NZ734194B2

NZ734194B2 - Methods of treating behavioral symptoms of neurological and mental disorders

Info

Publication number: NZ734194B2
Application number: NZ734194A
Authority: NZ
Inventors: James J Fallon; Joan M Fallon; Matthew F Heil; Kenneth Nanus; James Szigethy
Original assignee: Curemark Llc
Priority date: 2012-01-03
Filing date: 2013-01-03
Publication date: 2021-06-29

Abstract

Provided are uses of digestive enzymes in the manufacture of a medicament for the treatment of autism spectrum disorders. One embodiment provides the use of a composition that comprises a protease, an amylase, and a lipase for the manufacture of a medicament for the treatment of malnutrition as a result of self-imposed dietary restriction in a subject exhibiting an Autism Spectrum Disorder (ASD), wherein the medicament is formulated for administration to a subject two or more times a day with food and wherein upon administration of the medicament to the subject, the subject has an increase in the total daily fat, carbohydrate and/or vitamin intake (by weight) in comparison to intake before administration. sult of self-imposed dietary restriction in a subject exhibiting an Autism Spectrum Disorder (ASD), wherein the medicament is formulated for administration to a subject two or more times a day with food and wherein upon administration of the medicament to the subject, the subject has an increase in the total daily fat, carbohydrate and/or vitamin intake (by weight) in comparison to intake before administration.

Description

METHODS OF TREATING BEHAVIORAL SYMPTOMS OF NEUROLOGICAL AND MENTAL DISORDERS CROSS-REFERENCE This application claims the beneﬁt ofUS. Provisional Application No. 61/582,813, ﬁled January 3, 2012 and US. Provisional Application No. 61/600,110, ﬁled ry 17, 2012, which application is incorporated herein by reference in its entirety.

BACKGROUND OF THE INVENTION Autism is a lifelong disorder ofunknown origin. The disorder is characterized by behavioral, developmental, neuropathological, and sensory abnormalities (American Psychiatric Association 1994) and is usually sed between the ages of 3 and 10 with peak prevalence rates observed in children aged 5-8. gh there is debate as to whether autism has a pre- or post-natal origin, it is generally accepted that the ms and pathology persist throughout the life of the subject.

Nothing presented in the background section should be construed as an admission ofprior art.

SUMMARY OF THE INVENTION In one aspect a method is provided for treating a subject with an Autistic Spectrum Disorder (ASD), which es ive Developmental Disorders (PDDs), such as autism or an autistic disorder, in need thereofwith a ceutical composition comprising a therapeutic composition comprising proteases, amylases and/or lipases and an excipient: administering said pharmaceutical composition sing one or more pancreatic digestive enzymes to said subject, wherein said subject has an al fecal chymotrypsin level or stool pH, and wherein said subject shows a reduction in the severity or frequency of one or more symptoms associated with an Autistic Spectrum Disorder after stration of said pharmaceutical composition.

In another aspect a method is provided for treating a subject with an Attention Deﬁcit Disorder (ADD) and/or Attention Deﬁcit Hyperactivity Disorder (ADHD) in need thereofwith a pharmaceutical composition sing a therapeutic composition sing proteases, amylases and/or lipases and an excipient: administering said pharmaceutical composition comprising one or more pancreatic ive enzymes to said subject, wherein said subject has an abnormal fecal chymotrypsin level or stool pH, and wherein said subject shows a reduction in the severity or frequency of one or more symptoms associated with an Autistic Spectrum Disorder after administration of said pharmaceutical composition.

In another embodiment, one or more symptoms associated with an ic Spectrum Disorder and/or ADD or ADHD comprise bility, agitation, social awal, lethargy, inattention, hyperactivity, non-compliance, typy or inappropriate speech. In another embodiment the one or more ms comprise lethargy and hyperactivity, and/or the reciprocity of symptoms associated with each. In another ment, the symptoms are ed on the Aberrant Behavior Checklist (ABC) scale. In another embodiment, other measures are used to assess changes in autistic symptomotology as seen utilizing the behavioral and cognitive measures such as the Conners test, Expressive Vocabulary Test, second edition (EVT-2), Peabody Picture Vocabulary Test, fourth edition (PPVT-4), Social Communication Questionnaire (SCQ), The Autism Diagnostic iew-Revised (ADI-R test), the American atric Association's Diagnostic and Statistical Manual-IV (DSM-IV) test, any other test described herein or conventionally recognized in the art. In r embodiment, a pharmaceutical composition described herein does not produce a sedating effect, an se in neurological symptoms such as dizziness, dystonia, akathisia, somnolence, fatigue, extrapyramidal disorders, tremor, drooling, or other symptoms seen in medications treating behavioral disorders such as weight gain, etc. In another embodiment a pharmaceutical composition described herein does not produce a ng any side effects in accordance with FDA reporting standards (such as at a rate greater than about 5%).

In another embodiment, the subject is administered a ceutical composition described herein for at least 12 weeks. In one miting example, the subject is administered a pharmaceutical composition described herein three times a day for at least 12 weeks. In another embodiment, the subject showed said reduction in the severity or frequency of one or more symptoms after administration of a ceutical composition described herein for at least 12 weeks.

A subject to be treated with the methods described herein may be between the ages of 1-18 yrs. In another embodiment the subject is between the ages of 2-16 yrs. In another embodiment the subject is n the ages of 1-10 yrs. In another embodiment the subject is between the ages of 3-8 yrs. In another embodiment the subject is from any geographical location on the planet earth.

In another embodiment, the subject has mild and or moderate levels of lethargy, hyperactivity, social withdrawal or irritability prior to administration. In another embodiment the subject has high levels of lethargy, ctivity, social withdrawal or bility prior to administration.

In another embodiment the subject showed an improvement in receptive and/or expressive language after administration of a pharmaceutical composition described herein. In another embodiment the improvement is measured by the Expressive Vocabulary Test (EVT) and/or the Peabody Picture Vocabulary Test. In another embodiment the subject has autism and aphasia or another lack of expressive or receptive language.

In another ment the subject manifests one or more speech improvements, age appropriate grammatical structure and/or vocabulary after stration of a pharmaceutical composition described herein. In another embodiment the subject showed said station without a learning curve. In another embodiment the subject showed improvement in overall growth scales, increased question ceiling levels or reduction in error rates. In another embodiment the subject demonstrated improved working memory and/or ﬂuid reasoning after administration of a pharmaceutical composition described herein. In another embodiment the subject had reduced hyperactivity after administration of a pharmaceutical composition described herein. In another embodiment the changes in hyperactivity were observed in the Conners-3TR test. In r ment the one or more symptoms ses Inattention, Learning Problems, Executive ﬁanctioning, sion, Hyperactivity Impulsivity, Conduct Disorder, or Oppositional Deﬁance. In another embodiment the subject had improved Peer ons. In another embodiment the symptoms were measured on the Conners DSM-IV Scale.

In another embodiment the subject has increases in balanced food consumption, protein intake, vegetable intake, meat intake, terol, vitamin K, calcium, or improvements in glycemic load after administration of after ent with a pharmaceutical ition described herein compared to subject ofthe same age without an ASD or ADHD compared to a subject treated with a placebo. In r embodiment the subject has lower l caloric intake ed to subject of the same age without an ASD or ADHD or compared to a subject treated with a placebo. In another embodiment, the subject has the same l caloric intake after ent with a pharmaceutical composition described herein, but sed protein and fat intake compared to a subject treated with a placebo. In another embodiment the subject of the same age t an ASD, ADD or ADHD, or treated with a placebo, had a sedentary life style or an active life style. In another embodiment, a subject has fewer res after administration of a ceutical composition described herein compared to subject of the same age without an ASD or ADHD compared to a subject treated with a placebo.

In another embodiment, a subject exhibits improved overall health after administration of a pharmaceutical composition described herein ed to subject of the same age without an ASD or ADHD compared to a subject treated with a placebo. In another embodiment, a subject exhibits ed gastrointestinal health (e.g., improvement in constipation and/or diarrhea) after administration of a pharmaceutical composition described herein compared to subject ofthe same age without an ASD or ADHD ed to a subject treated with a placebo. In another embodiment, a subject exhibits a reduction in the number and/or severity of seizures (e.g., “Grand Mal”, absence, myoclonic, tonic, clonic or atonic) after administration of a ceutical composition described herein compared to subject ofthe same age without an ASD or ADHD compared to a subject treated with a placebo.

In another embodiment, an abnormal fecal chymotrypsin level indicates that said subject has physiological malnutrition. In another embodiment, the subject having a behavioral, neurological or mental er consumes fewer calories fat, protein, or carbohydrates than a subject with a normal fecal chymotrypsin level. In another embodiment the administration of a pharmaceutical ition described herein reverses the loss of protein and fat caloric ; in some cases, such intake occurs where the total caloric intake does not differ from a subject treated with a placebo. In another ment the subject is male. In another embodiment the subject is female. In another embodiment, the stool pH of a t treated with a pharmaceutical composition described becomes more ne.

The t may have a reduction in intake ofwhole grains after administration of a pharmaceutical composition described herein. The subject may also have a reduction in overall carbohydrate intake after administration of a pharmaceutical composition described herein. In another embodiment the reduction is at least 5%. In another embodiment the ion is at least 10%. In another embodiment the reduction is at least %. In another embodiment the ion is at least 20%. In another embodiment the reduction is at least 25%. In another embodiment the reduction is at least 30%. In another embodiment the reduction is at least 35%. In another ment the reduction is at least 40%. In another embodiment the reduction is at least 50%. In another embodiment the reduction is at least 60%. In another embodiment the reduction is at least 70%. In another embodiment the reduction is at least 80%. In another embodiment the ion is at least 90%. In another ment the reduction is at least 95%.

In another embodiment the administration of a pharmaceutical ition described herein is over a 4 week period. In another embodiment the administration of a pharmaceutical ition described herein is over an 8 week period. In another embodiment the administration of a pharmaceutical composition described herein is over a 12 week period. In another embodiment the stration of a pharmaceutical composition described herein is over a 16 week period. In another embodiment the administration of a pharmaceutical composition described herein is over a 20 week period. In another embodiment the administration of a pharmaceutical composition described herein is over a 6 month . In another embodiment the said administration of a pharmaceutical composition described herein is over a 1 year period. In another ment the said administration of a pharmaceutical composition described herein occurs on a regular, urring basis. A pharmaceutical ition described herein can be administered one, two or three times a day for the treatment period. A ceutical composition described herein can be administered with meals.

In another embodiment the subject increases overall protein intake aﬁer administration of a pharmaceutical composition described herein. In another embodiment the increase is at least 5%. In another embodiment the increase is at least 10%. In another embodiment the increase is at least 15%. In another embodiment the increase is at least %. In another embodiment the increase is at least 25%. In another embodiment the increase is at least 30%. In another embodiment the increase is at least 35%. In another embodiment the increase is at least 40%. In another embodiment the increase is at least 50%. In another embodiment the increase is at least 60%. In another embodiment the increase is at least 70%. In another embodiment the increase is at least 80%. In r embodiment the increase is at least 90%. In another embodiment the increase is at least 100%. In another embodiment the se is at least 150%. In another embodiment the increase is at least 200%.

In another embodiment the subject increases overall fat intake aﬁer administration of a pharmaceutical composition described herein. In another embodiment the increase is at least 5%. In another embodiment the increase is at least 10%. In another embodiment the increase is at least 15%. In r embodiment the increase is at least 20%. In r embodiment the se is at least 25%. In another embodiment the increase is at least 30%. In another embodiment the increase is at least 35%. In another embodiment the increase is at least 40%. In another embodiment the increase is at least 50%. In another embodiment the increase is at least 60%. In another embodiment the increase is at least 70%. In another embodiment the increase is at least 80%. In another embodiment the increase is at least 90%. In another embodiment the increase is at least 100%. In another embodiment the increase is at least 150%. In r ment the increase is at least 200%. In r embodiment the subject had a history of one or more allergies.

In r embodiment the subject with said history of one or more allergies had a larger intake of ﬁber, calories, fat, n, and carbohydrates aﬁer administration of a pharmaceutical composition described herein than a subject that did not have allergies. In another embodiment the t had an increase in B6, B12, A, C, E, K, Copper, Iron, Cholesterol, Niacin, vin, Thiamin, or Zinc consumption aﬁer administration of a pharmaceutical composition described herein. In another embodiment the subject had an increase in B6, B12, A, C, E, K, Copper, Iron, Cholesterol, Niacin, Riboﬂavin, Thiamin, or Zinc blood levels aﬁer administration of a pharmaceutical composition described herein. In another ment the subject ﬁlrther had a vitamin K deﬁciency. In another embodiment the vitamin K deﬁciency is measured by detecting levels of gamma carboxylated proteins in the blood. In another embodiment the method ﬁlrther comprises administering glutamate enhancing therapy to said subject. In another embodiment the method ﬁlrther comprises administering administration of vitamin K.

In another aspect a method is sed herein for treating a subject with an ASD, ADD or ADHD in need thereofwith a pharmaceutical composition described herein sing: administering said pharmaceutical composition comprising one or more pancreatic digestive enzymes to said subject, wherein said subject has a n K deﬁciency, and wherein said subject shows a reduction in the severity or ncy of one or more symptoms associated with an ASD, ADD or ADHD aﬁer administration of said pharmaceutical composition. In one embodiment the ASD is autism. In another embodiment the vitamin K deﬁciency is measured by detecting levels of gamma carboxylated proteins in the blood.

In another aspect a method is method of treating a t with an ASD, ADD or ADHD in need thereofwith a pharmaceutical composition described herein sing: administering said pharmaceutical ition comprising: 1) one or more pancreatic digestive enzymes; 2) glutamate enhancing therapy; and/or 3) vitamin K to said subject, wherein said t has a vitamin K deﬁciency or an abnormal fecal chymotrypsin level, 2013/020183 and n said subject shows a reduction in the severity or frequency of one or more symptoms associated with an ASD, ADD or ADHD after administration of said pharmaceutical composition. In one embodiment the ASD is autism. In another embodiment the vitamin K deﬁciency is measured by ing levels of gamma carboxylated proteins in the blood. In another embodiment a pharmaceutical composition described herein reduces the frequency or severity of diarrhea, gas, bloating, cramping, ﬂatulence, nausea or abdominal pain in said subject. In another embodiment the subject has stunting, protein energy malnutrition, wasting, n or mineral deﬁciency, abnormal albumin levels, abnormal umin levels, abnormal cholesterol levels, abnormal elastase levels or abnormal trypsin levels.

Provided herein is a method of treating a subject with an ASD, ADD or ADHD in need thereofwith a ceutical ition described herein comprising: administering said pharmaceutical composition comprising one or more digestive enzymes to said subject, wherein said subject has an abnormal fecal enzyme level, and wherein said subject shows a ion in the severity or frequency of one or more symptoms associated with an ASD, ADD or ADHD after stration of said pharmaceutical composition. In one aspect, the ASD is autism.

One or more symptoms that may be improve include, but are not limited to, irritability, agitation, social withdrawal, lethargy, hyperactivity, stereotypy and/or inappropriate speech. In one embodiment, the one or more ms include Lethargy and Hyperactivity.

Symptoms may be measured, for example, using the Aberrant Behavior Checklist (ABC) scale, any other test described herein and/or any other art-recognized test known in the art.

In such methods, a pharmaceutical ition described herein does not produce a sedating effect, an increase in neurological symptoms such as dizziness, son’s, dystonia, akathisia, ence, fatigue, extrapyramidal disorders, tremor, drooling, weight gain, or a combination thereof In one embodiment, a pharmaceutical composition described herein does not produce a sedating any side effects in accordance with FDA reporting standards (such as at a rate greater than 5%).

In another embodiment, a subject is administered a pharmaceutical composition described herein for at least 4 weeks. In one non-limiting e, a t shows a reduction in the severity or frequency of one or more symptoms after administration of said pharmaceutical composition for at least 4 weeks.

Subjects to be treated with such methods include children. In one embodiment, the child is male. In another embodiment, the child is female.

A t to be d with such methods may be from any geographical location on the planet earth. In one embodiment, the subject to be d is of Asian descent, of North American descent, of South American descent, of Eurasian descent, of Australian descent, of European descent, ofAfrican descent, or a combination thereof.

In one embodiment, a subject to be treated exhibits mild and or moderate levels of lethargy, hyperactivity, hypersensitivity, social withdrawal and/or irritability prior to administration of a pharmaceutical composition described herein.

In another embodiment, a subject to be treated exhibits t has high levels of lethargy, hyperactivity, hypersensitivity, social withdrawal or irritability prior to administration of a pharmaceutical composition described herein.

In one ment, the subject shows an improvement in receptive and/or expressive language after administration of a pharmaceutical composition described herein. Such improvements may be measured, for example, by the Expressive Vocabulary Test (EVT) and/or the y Picture Vocabulary Test. Subjects may be assessed prior to, during, and after treatment with any of the tests described herein.

In one embodiment, a subject to be treated with such methods has autism and aphasia or r lack of expressive language.

A subject treated with a pharmaceutical composition described herein may manifest one or more speech ements, age riate grammatical structure and/or vocabulary after administration of the pharmaceutical composition. In one embodiment, the subject may show the manifestation without a ng curve. In another embodiment, the subject show improvement in overall growth scales, sed question ceiling levels or reduction in error rates. In another embodiment, a subject demonstrates improved working memory and/or ﬂuid ing after administration of a pharmaceutical composition described . Such ements may be measured using a Stanford Binet Test. In another embodiment, a subject has reduced hyperactivity after administration of a pharmaceutical ition described herein. Such changes in hyperactivity may be observed in the Conners-3TR test.

In another aspect, symptoms to be treated by such methods include, but are not limited to, inattention, learning problems, ive ﬁanctioning, aggression, hyperactivity impulsivity, conduct er, oppositional defiance, or a combination thereof In one embodiment, a subject may have improved peer relations. Such symptoms may be ed, for example, on the Conners DSM-IV Scale.

In another aspect, a subject exhibits increases in ed food consumption, protein intake, vegetable intake, meat intake, cholesterol, vitamin K, m, and/or improvements in glycemic load aﬁer administration of a pharmaceutical composition described herein. In one embodiment, a subject has a lower overall caloric intake compared to a subject of the same age without an ASD or ADHD; where, in some cases, a subject of the same age without an ASD, ADD or ADHD had a sedentary life style or an active life style. In another embodiment, a subject has fewer fractures aﬁer administration of a pharmaceutical composition described herein.

An abnormal fecal enzyme level may indicate that the subject has physiological rition. In some cases, the al fecal enzyme level is an al fecal chymotrypsin level (FCT). Fecal enzyme levels may be monitored over time.

The amount of digestive enzymes stered to a subject may be based on one or more criteria including, but not limited to: said subject’s weight, said subject’s ne fecal chymotrypsin level, said subject’s instantaneous fecal chymotrypsin level, said subject’s time ed fecal chymotrypsin level, change in said subject’s chymotrypsin level, change in chymotrypsin level per unit time, rate of change of fecal rypsin level per unit time (2nd derivative), cumulative dose of digestive s to said subject to date, time averaged dosing over a given time period, rate of change of dosing against rate of change in fecal chymotrypsin level, or derivative of rate of change of dosing against rate of change in fecal chymotrypsin level.

In one embodiment, the fecal chymotrypsin level is used to titrate the amount of digestive enzymes administered to the subject.

A change in fecal chymotrypsin levels aﬁer administration of a pharmaceutical composition described herein, comprising one or more ive s may be used to determine when administration ofthe pharmaceutical composition comprising one or more digestive enzymes may be reduced, increased, or ated. In one embodiment, a subject to be treated has a low pre-treatment fecal chymotrypsin level. In one ment, a low fecal chymotrypsin level correlates to an increased severity in at least one symptom of autism. In another embodiment, decreasing levels of fecal chymotrypsin directly correlate with increasing severity of at least one symptom of autism. In yet another embodiment, improvements in the chymotrypsin level from baseline directly correlate with improvement of at least one symptom in the subject.

A subject to be treated with such methods may be diagnosed with autism neurological or mental disorder described herein. In one embodiment, the subject has a greater improvement in at least one symptom than a similar subject with a higher pretreatment fecal chymotrypsin level. In another embodiment, a t has a greater ement in post-treatment fecal chymotrypsin levels than a similar subject with a higher pretreatment fecal chymotrypsin level. The level of fecal chymotrypsin may be measured and used to titrate the amount of digestive enzymes administered to the subject.

In one , the pH of the subject’s stool returns to normal, or closer to normal, following treatment with a pharmaceutical composition described herein. In another aspect, the pH of the subject’s stool and the fecal chymotrypsin level of the subject return to normal, or closer to normal, following treatment with a composition described herein.

In another aspect, a subject exhibits an improvement in overall health following treatment with a pharmaceutical composition described herein. In one embodiment the improvement is a decrease in the rate or severity of ion. In another embodiment the improvement is a se in the number or severity of allergic incidents, which can include respiratory, dermatological, and/or gastrointestinal allergies.

In one aspect, a therapeutic composition disclosed herein comprises an amylase, a protease, or a lipase. In another aspect, a therapeutic composition disclosed herein ses two of: an amylase, a protease, and a lipase. In another aspect, a therapeutic composition disclosed herein ses an amylase, a protease, and a lipase.

In one aspect, the subject is ined or diagnosed as having at least one symptom of an ASD by using a screen comprising a DSM-IV, SCQ or ADI-R test. In r embodiment, a t is ined to have an ASD by using a screen comprising a DSM-IV, SCQ or ADI-R test. In one embodiment the subject is treated with a pharmaceutical ition described herein. In one embodiment the ASD is autism.

In one embodiment the subject is a child. In one embodiment the child is l, 2, 3, 4, ,5 ,6 7, 8,9 ,10, ll, 12, l3, 14, 15, l6, 17, or 18 years old.

In another embodiment, a subject is screened utilizing the ADI-R and determined to be able to be randomized for a clinical trial utilizing at least one or more of the following tests: ADI-R, DSM-IV and SCQ.

In another embodiment a subject with at least one symptom of an ASD and a level of chymotrypsin in a frozen stool sample <12.6 U/g is eligible for treatment with a ceutical composition disclosed herein.

In another ment a subject with at least one symptom of an ASD and a level of chymotrypsin in a fresh stool sample < 9 U/g is eligible for treatment with a pharmaceutical composition disclosed herein.

In another embodiment, a clinical trial with those with autism has a subset with those with abnormal chymotrypsin levels.

In another embodiment, a subject administered a pharmaceutical composition disclosed herein demonstrated higher fecal rypsin levels over the course of 12 weeks of administration.

In yet another embodiment, a pharmaceutical composition red chymotrypsin to the subject who was administered the pharmaceutical composition.

In another embodiment, there was a statistically signiﬁcant difference n subjects who were stered a pharmaceutical composition of (Formulation l) and ts who were administered a placebo.

In one embodiment a pharmaceutical composition comprises a therapeutic composition that comprises proteases, amylases and/or lipases, and/or an excipient. In one ment the therapeutic ition comprises proteases, amylases and lipases. In one embodiment the eutic composition is pancreatin. In one embodiment the therapeutic composition is coated with an excipient. In one embodiment the coating is a lipid or polymer coating. In one embodiment the g is a soy lipid coating, such as a soybean oil coating. The coating may optionally comprise an emulsifier. In one embodiment the pharmaceutical ition is provided as a tablet, capsule or granules.

In one embodiment the pharmaceutical composition has a protease actiVity of not less than 156 USP units/mg. In one embodiment the pharmaceutical composition is provided as granules. In one embodiment about 1.1 to 0.8 mg of the ceutical composition is provided per dose. In another embodiment the dose is provided in a pouch/sachet. In one embodiment, the pharmaceutical composition is Formulation l.

In another embodiment, a stool pH measurement is taken after treatment with a pharmaceutical composition disclosed herein of a subject with a symptom of an ASD, such as autism. In one embodiment the subject was diagnosed with autism before administration of the pharmaceutical composition disclosed . In one embodiment the stool pH becomes more alkaline after treatment of the subject with a pharmaceutical composition sed herein.

In another embodiment, the stool pH is measured to determine the gastrointestinal health of a subject with a symptom of an ASD, such as autism. In another embodiment, the stool pH is measured to determine the ability of a subject wit with a symptom of an ASD, such as autism to digest protein.

In another embodiment, a subject administered a pharmaceutical composition described herein exhibited a signiﬁcantly greater change in stool pH than a subject administered a placebo. In another embodiment, a subject administered a pharmaceutical composition described herein exhibited a positive change in stool pH demonstrating greater alkalinization of their stool, while a subject stered a placebo had an acidic change of their stool. In another embodiment, a subject administered a pharmaceutical composition described herein exhibited an alkalinization of their stool commencing at approximately week 4 aﬁer administration ofthe pharmaceutical composition began.

In one embodiment, an ABC test is used to e changes in one or more symptoms of an ASD in a subject administered a pharmaceutical ition described herein versus a subject administered a placebo. In another embodiment, a total ABC test is used to measure the outcomes tment of a subject with a pharmaceutical ition described herein. In one ment the t is a child. In one ment a total ABC test produces a total ABC scale. In another ment, the total ABC test can be used when a nd is non-sedating. In r embodiment, the total ABC scale can be used when the hyperactivity non-compliance scale and the lethargy social withdrawal scale are not ocal. In another embodiment, the total ABC scale or individual ABC subscales can be used to determine the outcomes of experimental observations in children with autism. In another embodiment, the ABC scale can be used when coupled with the ADI-R to determine the level of autism and the y to change based on the level of autism. In one embodiment, the one or more symptoms comprise irritability, agitation, social withdrawal, lethargy, hyperactivity, non-compliance, stereotypy or inappropriate speech. In another embodiment, the one or more ms comprise lethargy and hyperactivity the reciprocity of symptoms associated with each.

In another embodiment, the total ABC scale is used to measure change in autistic symptomotology. In another embodiment, the symptoms are measured on the Aberrant Behavior Checklist (ABC) scale, In another embodiment, other measures are used to assess changes in autistic symptomotology as seen using the behavioral and cognitive measures such as Conners test, EVT-2 test, PPVT-4 test, Social Communication Questionnaire, ADI-R test, the DSM-IV test, any other test described herein or conventionally recognized in the art.

In another ment, a pharmaceutical composition described herein does not produce a sedating effect, an increase in neurological symptoms such as dizziness, Parkinson’s, ia, akathisia, somnolence, fatigue, extrapyramidal disorders, tremor, drooling, or other symptoms seen in tions treating behavioral disorders.

In another embodiment, a pharmaceutical composition described herein does not produce any sedating any side effects in accordance with FDA reporting standards.

In another embodiment, the subject is administered a pharmaceutical composition described herein for at least 12 weeks. In another embodiment, the subject showed said reduction in the severity or frequency of one or more symptoms after administration of said pharmaceutical ition for at least 12 weeks. In another embodiment, the subject is administered said pharmaceutical composition for 24, 48 or additional weeks.

In r embodiment, the placebo adjusted 12 week scores demonstrated a significant difference between a subject administered a pharmaceutical composition bed herein and a subject administered a placebo as demonstrated by a greater percentage (%) change from baseline (i.e., before a pharmaceutical composition described herein was administrated). In one embodiment the subject is a child.

In another embodiment, that change as demonstrated by a continued increase in % change from baseline at 24 and 48 weeks shows a continued improvement over time in a t administered a pharmaceutical composition described . In one embodiment the subject is a child.

In yet another embodiment, the changes observed in a subject administered a pharmaceutical composition described herein, as measured by the ABC are in both positive and negative ms ofthe autism as measured by the ABC: positive ms (additive symptoms) hyperactivity, irritability, ion, stereopathy, and/or inappropriate speech. And the negative symptoms oms that take away behavior): social withdrawal, and lethargy.

In one ment, a subject treated with a ceutical composition described herein is between 1 and 18 years of age. In r embodiment, the subject is between the age of 2 and 16 years. In another embodiment, the subjects are between 3 and 8, in yet another embodiment the subjects are between 9 and 12 years of age. In another embodiment, the subjects are between the ages of 1 and 10 years. In one embodiment the subject is a child. In another embodiment, the subject is from any geographical location on the planet earth.

In another ment, a subject has mild and or moderate levels of gy, hyperactivity, social Withdrawal and/or irritability prior to administration. In another ment, a subject has high levels of lethargy, hyperactivity, social Withdrawal and/or bility prior to administration.

In another embodiment, a subject has mild and or moderate levels of hyperactivity and/or mpliance prior to administration. In another ment, a subject has high levels of hyperactivity and/or non-compliance prior to administration.

In another embodiment, a t has mild and or moderate levels of opriate speech prior to administration. In another embodiment, a subject has high levels of inappropriate speech prior to administration.

In another embodiment, the subject has mild and or moderate levels of stereopathy prior to administration. In r embodiment, the subject has high levels of stereopathy prior to stration.

In one embodiment, a PPVT and an EVT (A version or B versions) are used to measure vocabulary a method oftreatment of a subject (e.g., a child) with a pharmaceutical composition described . In one embodiment the subject has autism.

In another embodiment both a PPVT and an EVT are used to reduce pre-test post test bias out of the trial.

In another embodiment, the use ofthe PPVT coupled with the EVT is used to measure change in a subject for expressive and receptive language. In another embodiment the change is measured before the subject is administered a pharmaceutical composition described herein. In another embodiment the change is measured after the subject is administered a pharmaceutical composition described herein.

In another embodiment, the number of errors seen in the PPVT test in a subject is administered a pharmaceutical composition described herein is less than a subject administered a placebo.

In another embodiment, the growth scores seen in the PPVT test in a subject administered a pharmaceutical composition described herein is greater than a subject administered a o.

In another embodiment, the ceiling to error scores seen in the PPVT test ng minus (-) errors) is greater for a subject administered a pharmaceutical composition described herein.

In another embodiment, there is a r change for a subject administered a pharmaceutical composition described herein in the EVT growth score versus the PPVT score, demonstrating larger gains in expressive language.

In another embodiment, the number of errors seen in the EVT test in a subject administered a pharmaceutical composition described herein is less than a subject administered a placebo.

In another embodiment, the growth scores seen in the EVT tests in a subject administered a pharmaceutical composition described herein is greater than a t administered a placebo.

In another embodiment, the ceiling to error scores seen in the EVT test (ceiling minus (-) errors) is greater in a subject administered Formulation l, demonstrating improved performance.

In one embodiment, the block food screener is used to examine food intake by nutrient of a subject administered a ceutical composition described herein or of a subject administered a placebo. In another embodiment, the block food screener measures the qualitative and quantitative measure of food intake on a daily basis. In another embodiment, the block food screener measures ofthe qualitative and quantitative food intake can be compared to the changes in behavior, cognitive or other physiological measures in subjects with an ASD, such as autism, or other neurological disorders. In one embodiment, the changes as measured on the block food screener can be used to ine the nutritional status of a subject before, after or during stration of a pharmaceutical composition described herein. In yet r embodiment, as ed on the block food screener, as the ﬁnal amount of calories consumed per day at week 12 increased there are a greater improvement in scores on the total ABC. In yet another embodiment, as the total amount of calories consumed per day by a subject reached 800+ calories, as measured on the block food screener, the total ABC scores for a subject administered a placebo worsened while the total ABC score for a subject administered a ceutical composition described , improved cantly.

In another embodiment, there is improvement on the total ABC scores as seen in a t administered a ceutical composition described herein versus a subject administered a placebo at all levels of protein intake.

In another embodiment, at approximately 2+ grams of increase in protein intake per day as measured on the block food screener, a t administered a pharmaceutical 2013/020183 composition described herein has a greater improvement in at least one symptom ofASD, while a subject administered a placebo has a decline in at least one symptom ofASD.

In another embodiment, the worsening of ms on the total ABC in a subject administered a placebo is indicative of a lack of enzyme for the digestion of protein.

In yet r embodiment, there is improvement seen in subjects in their total ABC scores who are administered a pharmaceutical composition described herein versus subjects administered a placebo, at all levels of protein intake, as measured at 12 weeks after the pharmaceutical composition or placebo is ﬁrst administered.

In yet r embodiment, at imately 35+ grams of total protein intake per day as measured on the block food screener at week 12 administered a , subjects ceutical composition described herein began to have increased improvement, and subjects administered a placebo began to worsen in at least one m ofASD.

In yet another embodiment the worsening of symptoms on the total ABC administered a placebo is indicative of a lack of an enzyme for digestion of protein.

In one embodiment, there is improvement on total ABC scores in a subject administered a pharmaceutical ition described herein versus a subject stered a placebo at all levels of carbohydrate intake change as measured by the block food screener.

In yet another embodiment, at a level of 5+ grams change in carbohydrate intake as measured by the block food screener a subject administered a placebo began to worsen and a subject administered a pharmaceutical composition began to improve at a greater rate. In another embodiment, the worsening of symptoms as measured on the total ABC in a subject administered a placebo is due to the lack of enzyme to digest the n n of carbohydrates (such as gliadin n).

Provided herein is a method of treating a subject with one or more ms of an ASD, comprising: administering to the subject a pharmaceutical composition comprising one or more excipients and a therapeutic composition, wherein the therapeutic composition comprises protease, amylase and/or lipase, wherein the t exhibits improvement in one or more ms of an ASD comprising: (a) protein intake, fat intake, carbohydrate intake, Vitamin intake, diarrhea, constipation, seizures, and/or bone fragility; and/or (b) hyperactivity, irritability, agitation, obsessive compulsive behavior, eye contact, speech, lethargy, hypersensitivity, stereotypy, toilet training, non- compliance, inattention, and/or social withdrawal and wherein the subject has a greater improvement in the one or more symptoms of an ASD after administration ofthe pharmaceutical composition than a subject a subject with one or more ms of an ASD administered a placebo.

Improvement in one or more symptoms of an ASD may be at least 1 fold r improvement than in a subject with one or more symptoms of an ASD subject administered a placebo.

Improvement in one or more symptoms of an ASD may also be at least 2, 3, 4, or fold greater than in a subject with one or more symptoms of an ASD administered a placebo.

A subject may exhibit about a 10% or greater improvement in one or more symptoms of an ASD after administration ofthe pharmaceutical ition in comparison to before the subject was administered the pharmaceutical composition.

The subject may exhibit greater than about a 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90% or 100% improvement in the one or more symptoms of an ASD after administration of the ceutical composition.

Total daily protein, fat, carbohydrate and/or vitamin intake (by weight) by a subject may increase following administration of the pharmaceutical composition in ison to protein fat, carbohydrate and/or vitamin intake by the t before administration of the ceutical composition.

Total daily carbohydrate intake (by weight) by a subject may decrease following administration of the pharmaceutical composition in comparison to carbohydrate intake by the subject before administration of the pharmaceutical composition.

The subject may exhibit a greater increase in daily protein, fat, carbohydrate and/or n intake (by weight) following administration of the pharmaceutical composition in comparison to a subject with one or more symptoms of an ASD following administration of a placebo.

The greater the amount of daily protein, fat, carbohydrate and/or vitamin intake (by weight) consumed by a subject after administration of the pharmaceutical composition, the greater the subject’s improvement in one or more ms of an ASD.

In one embodiment, the daily n, fat, carbohydrate and/or vitamin intake (by weight) consumed by a subject may be measured before the subject was administered the pharmaceutical composition and at about 2, 4, 6, 8, 10, l2, l4, 16, 18, 20, 24, 36, 48 or 52 weeks after administration of the pharmaceutical composition begins. 2013/020183 A subject may exhibit a greater increase in daily vitamin intake (by weight) following administration of the pharmaceutical composition in ison to a subject with one or more symptoms of an ASD following administration of a o.

A subject may exhibit a greater increase in daily carbohydrate intake (by weight) following administration of the pharmaceutical composition in comparison to a subject with one or more symptoms of an ASD following administration of a placebo.

The total daily calories consumed by a subject may increase after administration ofthe ceutical composition in comparison to total daily calories consumed by a subject before administration of the pharmaceutical composition. The more daily calories the subject ed after administration of the pharmaceutical composition, the greater a subject’s improvement in one or more symptoms of an ASD.

The total amount of daily calories consumed by a subject may be measured before the subject is administered the pharmaceutical composition and at about 2, 4, 6, 8, , l2, l4, 16, 18, 20, 24, 36, 48 or 52 weeks after administration of the pharmaceutical ition begins.

In one embodiment, a subject may consume at least 800 kcalories per day after about 12 weeks of administration of the pharmaceutical composition.

A subject may ﬁarther exhibit an ement of a symptom comprising diarrhea, pation, seizures, bone fragility, hyperactivity, bility, agitation, obsessive compulsive behavior, eye contact, speech, lethargy, hypersensitivity, typy, toilet training, non-compliance, aggression, impulsivity, conduct er, or oppositional deﬁance and/or social withdrawal.

A subject’s improvement in one or more symptoms of an ASD may be measured on an Aberrant Behavior Checklist (ABC) scale.

A subject’s improvement in one or more ms of an ASD may be measured as a total Aberrant Behavior Checklist (ABC) score.

The daily protein intake of a subject may be higher after administration of the pharmaceutical composition begins compared to protein intake by the subject before stration of the pharmaceutical composition.

The daily protein intake of a subject may be higher after administration of the pharmaceutical composition begins compared to protein intake by the subject stered the placebo.

The daily n intake of a subject may be higher by 12 weeks after administration of the ceutical composition begins compared to protein intake by the subject before administration of the pharmaceutical composition.

The daily protein intake of a subject may be higher by 12 weeks after stration of the pharmaceutical ition begins compared to protein intake by a subject before administration of the pharmaceutical composition.

The daily protein intake of a subject may be about 2 grams higher by 12 weeks after administration of the pharmaceutical composition begins compared to daily protein intake by the subject before administration of the pharmaceutical composition.

The daily protein intake of a t may be about 2 grams higher by 12 weeks after administration of the pharmaceutical composition begins compared to daily protein intake by the subject before stration of the pharmaceutical composition.

A subject may consume from about 30 to about 50 grams ofprotein per day by 12 weeks after administration of the pharmaceutical composition begins.

A subject may consume about 35 grams or more ofprotein per day by 12 weeks after administration of the pharmaceutical composition begins.

] A subject may ﬁarther exhibit an improvement of a symptom comprising diarrhea, constipation, seizures, bone ity, hyperactivity, irritability, agitation, obsessive compulsive behavior, eye t, speech, lethargy, hypersensitivity, stereotypy, toilet training, non-compliance, aggression, impulsivity, conduct disorder, or oppositional deﬁance and/or social awal.

A subject’s improvement in one or more ms of an ASD may be ed as a total Aberrant Behavior Checklist (ABC) score.

The total daily calories consumed by a subject administered the pharmaceutical ition may be about the same as the subject consumed prior to administration of the pharmaceutical ition.

The total daily calories consumed by a subject administered the pharmaceutical composition may be about the same as a subject administered a placebo for the same length of time.

A subject may exhibit an improvement in carbohydrate intake of at least 3- grams per day.

A subject may exhibit an improvement in carbohydrate intake of at least 5 grams per day.

A Block Food Screener may be used to e food intake and/or to measure nutrient intake.

A Block Food Screener may be used to measure the quantity of food intake and/or to e quality of food intake.

] A subject may t improvement in hyperactivity by 12 weeks after administration of the pharmaceutical composition in comparison to a subject administered a placebo.

Hyperactivity may be measured by a Conners test.

A subject administered the pharmaceutical composition may show increased carbohydrate intake at week 12 in comparison to before the pharmaceutical composition was administered.

A subject may exhibit improvement in attention by 12 weeks after administration of the pharmaceutical composition in comparison to a t administered a placebo.

Attention may be measured by a Conners test.

A subject administered the pharmaceutical composition may show increased ydrate intake at week 12 in comparison to before the pharmaceutical ition was administered.

A subject may have a more alkaline stool pH after administration of the pharmaceutical ition than prior to administration of the pharmaceutical composition.

A subject may have a more alkaline stool pH after at least four weeks of administration of the pharmaceutical composition than prior to administration of the pharmaceutical composition.

A subject may have a more alkaline stool pH after administration of the pharmaceutical ition than the subject administered the placebo.

A subject may have a more alkaline stool pH after at least four weeks of administration of the pharmaceutical composition than prior to administration of the ceutical composition.

A subject may have an al fecal chymotrypsin level before administration of the pharmaceutical composition.

A subject may have a fecal chymotrypsin level less than 13 U/g as measured in a frozen stool sample before administration of the pharmaceutical composition.

] A subject may have a fecal chymotrypsin level less than 12.6 U/g as measured in a frozen stool sample before stration of the pharmaceutical composition.

A subject may have a fecal chymotrypsin level less than 10 U/g as measured in a fresh stool sample before administration of the pharmaceutical composition.

A subject may have fecal chymotrypsin levels less than 9 U/g as measured in a fresh stool sample before administration of the pharmaceutical composition.

A subject may have increased fecal chymotrypsin levels after administration of the pharmaceutical composition.

A subject may have increased fecal chymotrypsin levels after at least 12 weeks of administration ofthe pharmaceutical composition.

Improvement in one or more symptoms of an ASD may comprise an increase in protein intake, fat intake, carbohydrate intake, and/or vitamin intake in the subject.

Improvement in one or more symptoms of an ASD may comprise a decrease in carbohydrate intake.

Improvement in one or more symptoms of an ASD may comprise a decrease in the number of incidents or the severity of diarrhea, constipation, seizures, and/or bone fragility in the subject.

Improvement in one or more ms of an ASD may comprise a decrease in the number of incidents or the severity of ctivity, irritability, agitation, ive compulsive behavior, gy, hypersensitivity, stereotypy, non-compliance, aggression, impulsivity, conduct disorder, or oppositional e and/or social withdrawal in the subject.

Improvement in one or more symptoms of an ASD may comprise an increase in the number of incidents or on of eye contact.

Improvement in one or more ms of an ASD may comprise an increase in the number of incidents, articulation or vocabulary of the t’s speech.

Improvement in one or more symptoms of an ASD may se an improvement in toilet training.

Improvement may be ted by the subject administered the pharmaceutical composition and may be greater than the subject administered the placebo.

] A subject administered the pharmaceutical composition may ﬁarther have an improvement in overall health.

A subject may have a decrease in the number or severity of infections or a decrease in the number or ty of ic incidents after administration of the pharmaceutical composition in comparison to before the subject was administered the pharmaceutical composition.

A subject may have a decrease in the number or severity of infections or a decrease in the number or severity of allergic incidents after administration of the pharmaceutical ition in comparison to the subject administered the placebo.

A subject may be diagnosed as having an ASD before administration of the pharmaceutical composition.

A subject may be diagnosed as having an ASD by a DSM-IV, SCQ or ADI-R screen.

A subject may be diagnosed as having an ASD by a DSM-IV, SCQ or ADI-R screen, prior to administration of the pharmaceutical composition.

A subject may be diagnosed as having a PDD, ADD or ADHD.

A subject may be diagnosed as having autism.

One or more symptoms of an ASD may be measured for the subject using an Aberrant Behavior Checklist (ABC) scale, Conners test, sive Vocabulary Test (EVT) test, Peabody Picture Vocabulary Test (PPVT), Social ications Questionnaire (SCQ), ADI-R test, or DSM-IV test. In one ment, the EVT may be an EVT-2 test. In another embodiment, the PPVT may be a PPVT-4 test.

Hyperactivity may be measured by a Conners test.

In one ment, the Conners test may be a Conners-3 test.

Hyperactivity may be measured by comparing the Conners 3 test s with hyperactivity results measured on the ABC scale.

] One or more symptoms of an ASD may be measured prior to administration of the pharmaceutical composition.

One or more symptoms of an ASD may be measured after or during administration of the pharmaceutical composition.

WO 03746 ] One or more symptoms of an ASD may be measured one or more times after administration of the pharmaceutical composition for about 1, 2, 3, 4, 8, 12, 16, 20, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 70, 74, 78, 82, 86, or 90 weeks.

Improvement may be observed after the subject is stered the pharmaceutical composition for at least about 1, 2, 3, 4, 8, 12, 16, 20, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 70, 74, 78, 82, 86, or 90 weeks.

Improvement may be observed after the subject is stered the pharmaceutical composition for at least one week.

A subject may be administered the pharmaceutical composition with meals.

A subject may be administered the pharmaceutical composition daily. A subject may be administered the pharmaceutical composition 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12 times a day.

A subject may be administered the pharmaceutical composition once a day, twice a day or three time a day.

A subject may be administered the pharmaceutical composition for at least 12 weeks.

A subject may be administered the pharmaceutical composition for at least 3-6 months, 6-12 months, 12-18 months or 18-24 months.

A subject may be stered the pharmaceutical composition for at least 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 years.

The eutic composition may comprise proteases, amylases and lipases.

In one embodiment, the proteases se trypsin and/or rypsin.

In another embodiment, the therapeutic ition may be pancreatin.

In another embodiment, the therapeutic composition may be a solid form ofpancreatin.

In another embodiment, the therapeutic composition may be a crystalline form ofpancreatin.

In one embodiment, the pharmaceutical composition does not produce a sedating effect, an increase in ess, Parkinson’s disease symptoms, dystonia, akathisia, somnolence, fatigue, extrapyramidal ers, tremor, or drooling.

In another ment, the therapeutic composition comprises a coating.

The coating may be an enteric coating.

The coating may comprise a lipid, a lipid mixture, a blend of lipid and emulsiﬁers, or a polymer.

In one ment, the coating comprises a soy lipid.

The coating may mask the task and/or smell ofthe therapeutic composition.

In another embodiment, the enteric coating comprises hypromellose phthalate, dimethicone 1000, dibutyl ate, or a combination thereof.

The coating may ﬁlrther comprise an ﬁer.

The one or more excipients may comprise a cellulose.

] The therapeutic composition may be released into the proximal small intestine ing administration to the subject.

The therapeutic composition may be released into the um or jejunum portion of small intestine following administration to the subject.

The therapeutic composition may be ed into the ileum portion of small intestine following administration to the subject.

The pharmaceutical composition may be administered by oral administration.

The pharmaceutical composition may be administered directly into the gastrointestinal system.

The pharmaceutical composition may be administered through a nasal- intestinal —tube (NG Tube) or gastrointestinal —tube (G-tube).

A subject administered the pharmaceutical composition may exhibit improvement in two, three, four, ﬁve, six or more symptoms of an ASD.

] A subject may be between the ages of 1-18 years. A subject may be between the ages of 2-16 years. A subject may be between the ages of 1-10 years. A subject may be between the ages of 3-8 years. A subject may be between the ages of 9-12 years.

A subject may exhibit an increase in vitamin intake (by weight) of B6, B12, A, C, E, K, Copper, Iron, terol, Niacin, vin, Thiamin, or Zinc after administration of the pharmaceutical composition.

A subject may exhibit an increase in vitamin intake of one or more of plant based Vitamin A, Carotenoids (alpha and beta carotene), Vitamin K, Vitamin E, n C, Selenium, copper, folate, lutein, lycopene, magnesium, potassium, phosphorus, sodium, saturated fatty acids, monounsaturated fatty acids, saturated fats, terol, Vitamin E, Vitamin K, and/or Theobromine.

The increase in Vitamin intake by the subject may be in comparison to before the subject began administration of the ceutical composition.

The increase in Vitamin intake by the subject may be in comparison to the subject stered the placebo.

A subject may exhibit an increase in B6, B12, A, C, E, K, Copper, Iron, Cholesterol, Niacin, Riboﬂavin, Thiamin, or Zinc blood levels after administration of the pharmaceutical ition A t may exhibit an increase in fecal levels of plant based Vitamin A, noids (alpha and beta carotene), Vitamin K, Vitamin E, Vitamin C, Selenium, copper, folate, lutein, lycopene, magnesium, potassium, phosphorus, , polyunsaturated fatty acids, monounsaturated fatty acids, saturated fats, cholesterol, Vitamin E, Vitamin K, and/or omine.

] The increase in blood or fecal levels of the subject may be in comparison to before the subject began administration of the pharmaceutical composition.

The increase in blood or fecal levels by the subject administered the pharmaceutical composition may be in comparison to the subject administered the placebo.

In r embodiment, the subject ﬁarther has a Vitamin K deficiency.

The Vitamin K deficiency may be measured by detecting levels of gamma carboxylated proteins in the blood.

In one embodiment, the method ﬁarther comprises administering glutamate ing therapy to the subject.

In another embodiment, the method r comprises administering administration ofVitamin K.

Provided herein is a method of improving expressive and/or receptive ge capabilities a subject with a symptom of an ASD, comprising administering a pharmaceutical composition comprising one or more excipients and a therapeutic composition, wherein the therapeutic composition comprises protease, amylase and/or lipase.

A subject may exhibit an improvement in expressive and/or receptive language capabilities after administration of the pharmaceutical composition in comparison to before the subject was administered the pharmaceutical composition.

A subject may exhibit a greater improvement in expressive and/or receptive language capabilities after stration of the pharmaceutical ition than a subject with a m of an ASD administered a placebo.

The expressive and/or ive language lities may be measured with an Expressive Vocabulary Test (EVT) and/or Peabody Picture lary Test (PPVT).

In one ment, the EVT test may be an EVT-A or EVT-B test.

In one embodiment, the PPVT test may be a PPVT-A or PPVT-B test.

A subject administered the ceutical composition may t a greater improvement in expressive language capabilities than receptive language capabilities.

Provided herein is a method of treating a subject with one or more symptoms of an ASD, comprising: administering to the subject a ceutical composition comprising one or more excipients and a therapeutic composition, wherein the therapeutic composition comprises protease, amylase and/or lipase, wherein the subject exhibits improvement in one or more symptoms of an ASD comprising: (a) protein intake, fat intake, carbohydrate intake, vitamin intake, seizures, and/or bone fragility; and/or (b) irritability, agitation, lethargy, hypersensitivity, non-compliance, sion, impulsivity, conduct disorder, or oppositional deﬁance and/or social withdrawal and wherein the subject has at least a 10% or greater improvement in the one or more symptoms of an ASD after administration ofthe pharmaceutical composition.

A subject may exhibit increases l fat intake (by weight) of at least about 10% after administration of the pharmaceutical composition.

A subject may exhibit increases overall protein intake (by ) of at least about 10% after administration of the pharmaceutical composition.

A t may exhibit increases overall carbohydrate intake (by weight) of at least about 10% after stration of the pharmaceutical composition.

Provided herein is a method of increasing body mass or physical growth in a subject with a symptom of an ASD, comprising administering a pharmaceutical composition comprising one or more excipients and a therapeutic composition, wherein the therapeutic composition comprises protease, amylase and/or lipase.

A subject may be sed as having an ASD before administration of the pharmaceutical composition.

WO 03746 A subject may be diagnosed as having an ASD by a DSM-IV, SCQ or ADI-R .

A subject may be diagnosed as having an ASD by a DSM-IV, SCQ or ADI-R screen, prior to administration of the pharmaceutical ition.

A subject may be diagnosed as having a PDD, ADD or ADHD.

A t may be diagnosed as having autism.

] One or more symptoms of an ASD may be measured for the subject using an Aberrant Behavior Checklist (ABC) scale, Conners test, Expressive Vocabulary Test (EVT) test, Peabody Picture Vocabulary Test (PPVT), Social Communications Questionnaire (SCQ), ADI-R test, or DSM-IV test. In one embodiment, the EVT may be an EVT-2 test. In another embodiment, the PPVT may be a PPVT-4 test. Hyperactivity may be measured by a Conners test.

In another embodiment, the Conners test may be a Conners-3 test.

Hyperactivity may be measured by comparing the Conners 3 test results with ctivity results measured on the ABC scale.

The one or more symptoms of an ASD may be measured prior to administration of the ceutical composition.

The one or more symptoms of an ASD may be measured after or during administration of the pharmaceutical composition ement may be observed in the subject administered the pharmaceutical composition 12 weeks or more after the t began administration of the pharmaceutical composition.

] A subject administered the pharmaceutical composition may exhibit a greater improvement in an EVT score than a PPVT score.

A subject administered the pharmaceutical composition may exhibit a greater improvement in EVT or PPVT score and the subject may t increased protein intake after the subject began administration of the pharmaceutical composition.

Improvement may be observed 12 or more weeks after the subject begins administration of the pharmaceutical composition.

A subject may exhibit greater than a 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90% or 100% improvement in one or more additional symptoms of an ASD after administration of the pharmaceutical composition.

] Total daily n, fat, carbohydrate and/or vitamin intake (by weight) by the subject may increase following administration of the pharmaceutical composition increases in comparison to protein, fat carbohydrate, and/or Vitamin intake by the subject before administration of the pharmaceutical ition.

Total daily carbohydrate intake (by weight) by the subject may decrease following administration of the pharmaceutical composition in comparison to carbohydrate intake by the subject before administration of the pharmaceutical ition.

A subject may exhibit a greater increase in daily protein, fat, carbohydrate and/or Vitamin intake (by weight) following administration of the pharmaceutical composition in comparison to a t with one or more symptoms of an ASD ing administration of a placebo.

] The greater the amount of daily protein, fat, carbohydrate and/or Vitamin intake (by weight) consumed by the subject after administration of the pharmaceutical composition, the greater the subject’s improvement in one or more symptoms of an ASD.

The daily protein, fat, carbohydrate and/or Vitamin intake (by weight) consumed by the subject may be measured before the subject was administered the pharmaceutical composition and at about 2, 4, 6, 8, 10, l2, l4, 16, 18, 20, 24, 36, 48 or 52 weeks after administration of the pharmaceutical composition begins.

A subject may have a greater se in daily Vitamin intake (by weight) following administration of the pharmaceutical composition in comparison to a subject with one or more symptoms of an ASD ing administration of a placebo.

A subject may have a greater increase in daily carbohydrate intake (by weight) ing administration of the pharmaceutical composition in comparison to a subject with one or more symptoms of an ASD following administration of a placebo.

The total daily calories consumed by the subject may increase after administration of the pharmaceutical composition in comparison to total daily calories ed by the t before administration of the pharmaceutical composition.

The more daily es the subject consumed after administration of the pharmaceutical composition, the greater the subject’s improvement in one or more symptoms of an ASD.

] The total amount of daily calories consumed by the subject may be measured before the subject may be administered the pharmaceutical composition and at about 2, 4, 6, 8, 10, l2, l4, l6, 18, 20, 24, 36, 48 or 52 weeks after administration ofthe pharmaceutical composition begins.

A subject may consume at least 800 kcalories per day after about 12 weeks of administration of the ceutical composition.

A subject may ﬁarther exhibit an improvement of a symptom comprising diarrhea, constipation, seizures, bone fragility, and/or hyperactivity.

A subject may have a more alkaline stool pH after stration of the pharmaceutical composition than prior to administration of the pharmaceutical composition.

A subject may have a more alkaline stool pH after at least four weeks of administration of the pharmaceutical composition than prior to administration of the pharmaceutical ition.

A subject may have a more alkaline stool pH after administration of the pharmaceutical composition than the subject administered the placebo.

A subject may have an abnormal fecal chymotrypsin level before stration of the pharmaceutical composition.

A subject may have a fecal chymotrypsin level less than 13 U/g as measured in a frozen stool sample before administration of the ceutical composition.

A subject may have a fecal chymotrypsin level less than 12.6 U/g as measured in a frozen stool sample before administration of the pharmaceutical composition.

A subject may have a fecal rypsin levels less than 9 U/g as measured in a fresh stool sample before administration of the pharmaceutical composition.

A subject may have an sed fecal rypsin levels after administration of the ceutical composition.

A t may have an increased fecal chymotrypsin levels after at least 12 weeks of administration ofthe pharmaceutical composition.

A subject may ﬁarther have an improvement in one or more additional symptoms of an ASD.

The one or more ms of an ASD may be measured prior to stration of the pharmaceutical composition.

The one or more symptoms of an ASD may be measured after or during administration of the pharmaceutical composition.

The one or more symptoms of an ASD may be measured one or more times after administration of the pharmaceutical composition for l, 2, 3, 4, 8, l2, 16, 20, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 70, 74, 78, 82, 86, or 90 weeks.

] Improvement may be observed after the t may be stered the pharmaceutical composition for at least I, 2, 3, 4, 8, l2, 16, 20, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 70, 74, 78, 82, 86, or 90 weeks.

Improvement may be observed after the subject may be administered the pharmaceutical composition for at least one week.

A subject may be administered the pharmaceutical composition with meals.

A subject may be stered the pharmaceutical composition daily.

A subject may be administered the pharmaceutical composition 1, 2, 3, 4, , 6, 7, 8, 9, 10, ll or l2times a day.

A subject may be administered the ceutical composition once a day.

A subject may be administered the pharmaceutical composition for at least 3-6 months, 6-l2 months, 12-18 months or 18-24 months.

A subject may be administered the pharmaceutical composition for at least 1,2, 3,4, 5, 6, 7, 8, 9 or 10 years.

In one embodiment, a therapeutic composition comprises proteases, amylases and lipases.

In another embodiment, the proteases comprise n and/or chymotrypsin.

] In another embodiment, the therapeutic composition may be pancreatin.

In r embodiment, the therapeutic composition may be a solid form ofpancreatin.

] In another embodiment, the eutic composition may be a crystalline form ofpancreatin.

In another embodiment, the ceutical ition does not produce a sedating effect, an increase in dizziness, son’s disease symptoms, dystonia, akathisia, somnolence, fatigue, extrapyramidal disorders, tremor, or ng.

The therapeutic composition may comprise a coating.

The coating may be an enteric coating.

The coating may comprise a lipid, a lipid mixture, a blend of lipid and emulsifiers, or a polymer.

In one embodiment, coating comprises a soy lipid.

The coating may mask the task and/or smell ofthe therapeutic composition.

In one embodiment, the enteric coating comprises hypromellose phthalate, dimethicone 1000, dibutyl phthalate, or a combination thereof The coating may ﬁarther comprise an emulsifier.

In any of such embodiments bed herein, the one or more excipients comprise a cellulose.

The eutic composition may be released into the proximal small intestine following administration to the subject.

The therapeutic composition may be released into the duodenum or jejunum portion of small intestine following administration to the subject.

The therapeutic ition may be released into the ileum portion of small intestine following administration to the subject.

The pharmaceutical composition may be administered by oral administration.

The ceutical composition may be administered ly into the gastrointestinal system.

The pharmaceutical composition may be administered through a nasal- gastrointestinal —tube (NG Tube) or intestinal —tube (G-tube).

A t administered the pharmaceutical composition may exhibit improvement in two, three, four, ﬁve, six or more symptoms of an ASD.

A subject may be between the ages of l-l8 years. A subject may be between the ages of 2-16 years. A subject may be between the ages of l-lO years. A t may be n the ages of 3-8 years. A subject may be between the ages of 9-12 years.

A subject may exhibit an increase in vitamin intake (by weight) of B6, B12, A, C, E, K, , Iron, Cholesterol, Niacin, Riboﬂavin, Thiamin, or Zinc after administration of the pharmaceutical composition.

A subject may exhibit an increase in vitamin intake of one or more of plant based Vitamin A, Carotenoids (alpha and beta carotene), Vitamin K, Vitamin E, n C, Selenium, copper, folate, , lycopene, magnesium, potassium, phosphorus, sodium, polyunsaturated fatty acids, monounsaturated fatty acids, saturated fats, cholesterol, vitamin E, Vitamin K, and/or Theobromine.

The increase in vitamin intake by the subject may be in comparison to before the t began administration of the pharmaceutical composition.

The increase in n intake by the subject may be in comparison to the subject administered the placebo.

A subject may exhibit an increase in B6, B12, A, C, E, K, Copper, Iron, Cholesterol, Niacin, Riboﬂavin, Thiamin, or Zinc blood levels after administration of the pharmaceutical composition A subject may exhibit an increase in fecal levels of plant based Vitamin A, Carotenoids (alpha and beta carotene), Vitamin K, Vitamin E, Vitamin C, Selenium, copper, folate, lutein, ne, magnesium, potassium, phosphorus, sodium, polyunsaturated fatty acids, monounsaturated fatty acids, saturated fats, cholesterol, vitamin E, Vitamin K, and/or Theobromine.

The increase in blood or fecal levels of the subject may be in comparison to before the subject began administration of the ceutical composition.

Provided herein is a method of treating a subject with a PDD, ADD or ADHD in need thereofwith a pharmaceutical composition comprising: administering the pharmaceutical composition comprising one or more pancreatic ive enzymes to the subject, n the subject shows a reduction in the severity or frequency of one or more symptoms associated with a PDD, ADD or ADHD after stration ofthe pharmaceutical composition. ed herein is a method of treating a subject with a PDD, ADD or ADHD in need thereofwith a pharmaceutical composition sing: administering the pharmaceutical composition comprising one or more atic digestive enzymes to the subject, wherein the t has a Vitamin K deﬁciency, and wherein the subject shows a reduction in the severity or ncy of one or more symptoms associated with a ASD, ADD or ADHD after administration ofthe pharmaceutical composition.

The ASD may be autism.

The Vitamin K ncy may be measured by detecting levels of gamma carboxylated proteins in the blood.

Provided herein is a method of treating a t with a ASD, ADD or ADHD in need thereofwith a pharmaceutical composition comprising: administering the pharmaceutical composition comprising: 1) one or more atic digestive enzymes; 2) glutamate enhancing therapy; and/or 3) Vitamin K to the subject, wherein the subject has a Vitamin K deﬁciency or an abnormal fecal chymotrypsin level, and wherein the subject shows a reduction in the severity or frequency of one or more symptoms associated with a ASD, ADD or ADHD after administration ofthe pharmaceutical ition.

The ASD may be autism.

The Vitamin K ncy may be measured by detecting levels of gamma carboxylated proteins in the blood. ] ed herein is a method of treating a subject with a ASD, ADD or ADHD in need thereofwith a pharmaceutical composition sing: administering the pharmaceutical composition comprising one or more pancreatic digestive enzymes to the subject, wherein the subject has a Vitamin K deﬁciency, and wherein the subject shows a reduction in the ty or frequency of one or more symptoms associated with a ASD, ADD or ADHD after administration ofthe pharmaceutical composition.

Provided herein is a method of treating a subject with one or more ms of an ASD, comprising: administering to the subject a pharmaceutical composition comprising one or more excipients and a therapeutic composition, wherein the therapeutic composition comprises protease, amylase and/or lipase, wherein the subject exhibits improvement in one or more symptoms of an ASD, wherein the subject has one or more allergies and has a larger intake of ﬁber, calories, fat, protein, and carbohydrates after administration of the pharmaceutical composition than a subject that did not have allergies.

INCORPORATION BY REFERENCE All publications, patents, and patent applications mentioned in this cation are herein incorporated by reference to the same extent as if each individual publication, patent, or patent application was speciﬁcally and individually indicated to be orated by reference. US Publication No. 2010-0260857 Al (USSN 12/386051) by Fallon and Heil is incorporated by reference herein in its entirety.

BRIEF DESCRIPTION OF THE DRAWINGS ] The novel features of the ments are set forth with particularity in the appended claims. A better understanding ofthe features and ages of the present embodiments will be ed by reference to the following detailed description that sets forth rative embodiments, in which the principles of the embodiments are utilized, and the accompanying drawings h: Figure 1 shows a bar graph of the % lipase activity in the raw digestive enzyme particles, and following encapsulation, for coated enzyme ations containing 70%, 80% and 90% digestive enzymes by weight; Figure 2 shows a bar graph ofthe % enzyme release for the enzyme preparations ning 70%, 80% and 90% digestive enzymes by weight, at the times indicated on the y-aXis; Figure 3 shows a bar graph ofthe particle size distributions of the raw digestive enzyme particles compared with the particle size distributions in coated enzyme preparations containing 70% or 80% digestive enzymes by ; Figure 4 shows the ﬂow chart for a process that can be used to encapsulate digestive enzyme particles; Figure 5 shows a chromatogram ofpeak area (mAU) vs. time for working standard (top line), diluent (line that starts third from the top when time is 4 minutes), mobile phase used in the HPLC (bottom line at 4 minutes) and placebo (second to the top line when time is 4 minutes), which demonstrate no interference with the standard trypsin peak.

Figure 6 shows FCT levels ed in 26 subjects with symptoms of autism.

Figure 7 shows FCT levels measured in 46 subjects. 25 ofthe subjects had symptoms of autism, while 21 subjects did not have symptoms of autism.

Figure 8 shows fecal chymotrypsin levels measured in 320 age-matched subjects. The navy line (in grayscale, the upper, black line) shows FCT levels for ts with known ions (genetic and other conditions). The purple line (in grayscale, the upper, dark gray line), shows FCT levels for normal ts without any known ion. The aqua line, (in gray scale, the lower, medium gray line), shows FCT levels for subjects with autism. The pink line (in gray scale, the lower, dark gray line), shows FCT measurements for subjects with ADHD. The yellow line (in grayscale, the lower, light gray line), shows FCT measurements for subjects with ADD.

Figure 9 illustrates abnormal chymotrypsin levels in various subject populations.

Figure 10 provides an exemplary dietary outcome of self-imposed dietary restrictions observed in autistic subjects.

Figure ll provides Fecal rypsin .

] Figure 12 provides Fecal Chymotrypsin levels.

] Figure 13 provides exemplary major proteases.

Figure 14 illustrates representative movement of protein through the body after intake.

Figure 15 shows the changes in fecal rypsin levels from baseline in subjects administered the Formulation 1 versus ts administered the placebo.

Figure 16 illustrates the pH change in subjects treated with Formulation 1 versus placebo during the 12-week clinical trial.

Figure 17 shows the PPVT results the growth scores for subjects on Formulation l exceeded those on the placebo. Growth scores are adjusted for age and for standardization of scores across the entire study.

Figure 18 shows the EVT scores demonstrate a large difference between ts administered the Formulation l and subjects administered the placebo.

Figure 19 illustrates the EVT mean standard score change as a ﬁanction of protein intake (g) at week 12.

Figure 20 illustrates the total ABC median analysis at baseline total ABC change over the course of the 12-week trial.

Figure 21 illustrates the ABC irritability change as a ﬁanction of fecal chymotrypsin at week 12. At week 12 there is a statistically significant difference between placebo and Formulation 1 subjects in the irritability scores on the ABC regardless of their level of fecal chymotrypsin at week 12.

Figure 22 rates the ABC irritability score change in subjects above the ABC median irritability at baseline. In subjects whose baseline median ABC subscale for irritability was above the median at baseline, Formulation 1 improved signiﬁcantly over Placebo.

Figure 23 illustrates the ABC irritability change as a ﬁanction of protein intake change at week 12. There is a difference between the Formulation 1 subjects and the placebo subjects with respect to the ABC Irritability changes during the trial. The subjects on Formulation 1 had a greater change compared to the placebos regardless of the protein intake change over the course of the trial. Of note at about a 4 g+ increase in Protein intake per day, the ABC Irritability change continues to improve in the Formulation 1 subjects, and it worsens in the o ts.

Figure 24 illustrates the ABC irritability change as a ﬁanction of n intake (g) at week 12. There is a ence between the Formulation 1 subjects and the placebo subjects with respect to the ABC Irritability changes during the trial. The subjects on Formulation 1 had a greater improvement in ABC irritability scores compared to the placebos regardless of the protein intake at week 12. Of note, at about a 40 g+ in overall protein intake, the ABC Irritability change remains relatively constant in the Formulation 1 subjects, and it worsens in the placebo subjects. The greater the protein intake at week 12 in the ation 1 subjects the ABC bility scores are constant, and in the placebo the greater the protein intake at week 12, the worse subjects did on the ABC Irritability scale, and the change in the placebo scores went down.

Figure 25 illustrates the ABC irritability change as a ﬁanction of carbohydrate intake change. Regardless ofthe carbohydrate intake change during the trial, subjects administered Formulation 1 improved cantly (lower number) over subjects on the placebo. There also was a worsening in subjects on placebo as the carbohydrate (CHO) levels increase above 25+ grams.

Figure 26 illustrates the ABC irritability change as a ﬁanction orie intake at week 12. ABC irritability change improvement was greater in subjects on Formulation l regardless of the levels of calorie intake as ed at week 12. The ation 1 group irritability improvement change remained steady regardless of the c intake level as measured during week 12. The placebo group worsened in their irritability change as the level of calories measured was . It was especially noticeable at 800+ total calorie intake. It is important to note that these levels below 1200 calories are all abnormal levels of caloric intake.

Figure 27 rates the ABC lethargy change as a on ofkCalorie intake at week 12. Subjects on Formulation 1 had a great improvement in Social Withdrawal/ Lethargy compared to subjects on placebo regardless of amount caloric intake. When subjects on placebo reached approximately 800+ calories per day in intake they started to worsen.

] Figure 28 illustrates the ABC lethargy change as a ﬁanction of protein intake . ts on Formulation 1 had greater improvement in lethargy/social withdrawal compared to subjects on the placebo regardless of the protein . Subjects who had a 2+ gram change on the placebo continued to worsen with increasing amount of change from baseline in protein consumption.

Figure 29 rates the ABC lethargy change as a ﬁanction of fecal chymotrypsin at week 12. Subjects on ation 1 had greater improvement in lethargy/social withdrawal compared to subjects on the placebo regardless of their fecal chymotrypsin levels at week 12. Subjects who had a fecal chymotrypsin level of 8+ units/g or greater at week 12 and received Formulation 1 improved more than subjects administered a placebo, who had levels of fecal chymotrypsin at 8+ U/g, improved even more. Subjects who were on the placebo continued to worsen with increasing levels of FCT at the end ofthe trial.

Figure 30 illustrates the ABC ctivity change as a ﬁanction of kCalorie intake at week 12.

Figure 31 illustrates the ABC hyperactivity change as a ﬁanction of protein intake (g) at week 12.

Figure 32 illustrates the ABC hyperactivity change as a on of fecal chymotrypsin at week 12.

Figure 33 illustrates the ABC stereotypy change as a ﬁanction orie Intake at week 12.

Figure 34 rates the ABC stereotypy change as a ﬁanction of n intake (g) at week 12.

Figure 35 illustrates the ABC speech change as a ﬁanction ofkCalorie intake at week 12.

Figure 36 illustrates the ABC inappropriate speech change as a ﬁanction of protein intake change at week 12.

Figures 37A-B illustrate the total ABC median is at baseline: total ABC change over the l2-week trial. The overall measure ofABC change demonstrated that subjects above the median at baseline responded more robustly to Formulation 1 over subjects treated with placebo. Results below the median are shown in Figure 37A; results above the median are shown in Figure 37B.

Figure 38 illustrates the total ABC change as a ﬁanction okaalorie intake at week 12.

] Figure 39 illustrates the total ABC change as a ﬁanction of protein intake change at week 12.

Figure 40 illustrates the total ABC change as a ﬁanction of protein intake (g) at week 12.

] Figure 41 illustrates the total ABC change as a ﬁanction of fecal chymotrypsin at week 12. There is a signiﬁcant difference between subjects stered Formulation l and subjects administered placebo in their total ABC change regardless of their level of fecal chymotrypsin at week 12. This is suggestive of the fact that it is not just the rypsin levels g the process of change from the enzyme ition.

Figure 42 illustrates the total ABC change as a ﬁanction of carbohydrate intake change at week 12.

Figure 43 illustrates the kCalorie change as a ﬁanction of carbohydrate intake change. Subjects treated with Formulation l in the trial had a greater change in their kcal consumption compared to the placebo subjects regardless of the level of the increase in change in ydrate (CHO) consumption. There continues to be a separation between the Formulation l and subjects treated with placebo over the course of treatment.

Figure 44 rates the protein intake change as a ﬁanction of carbohydrate intake change. Regardless ofthe change in protein intake over the course of the trial or the CH0 intake, there continues to be a tion between the two .

Furthermore, regardless of the protein intake change, overall n intake is greater in subjects treated with Formulation 1 group over subjects treated with placebo, regardless ofthe change in CHO consumption.

Figure 45 illustrates the protein intake at week 12 as a ﬁanction of carbohydrate intake . The absolute amount ofprotein ingested by subjects at week 12 ofthe trial was greater in subjects on Formulation 1 compared to subjects receiving placebo. The CHO intake change over the course ofthe trial does not drive the amount of protein subjects ate at week 12. Once again, it was observed that the changes occurred in subjects on the drug compared to subjects on placebo. Of note is that once 20 g+ change in the CH0 ingestion over the trial, there is a greater separation between subjects ing Formulation 1 versus placebo.

Figure 46 illustrates the n change as a ﬁanction of carbohydrate intake change. Protein intake change over the course of the trial was greater in subjects administered Formulation 1 than in subjects administered placebo regardless of the level ofCHO intake change over the course ofthe trial. The increases in protein intake in subjects administered the drug were not driven by the CH0 intake.

] Figure 47 illustrates the kCalorie Change as a Function of Carbohydrate Intake Change. The graph demonstrates that ts treated with Formulation 1 have a greater kcal change across all increases in CHO ingestion during the trial. ts treated with Formulation 1 exhibited increases in CHO ingestion during the trial also had a greater kcal change compared to subjects treated with placebo. This trates that the carbohydrate ingestion during the trial even great changes up to 30+ g/day did not drive the increases in kcal consumption during the 12 weeks of the trial.

Figure 48 illustrates the mean fecal chymotrypsin at seek 12 as a on of carbohydrate (g) intake change: both subjects treated with Formulation 1 and subjects treated with placebos exhibited means similar at ne. The mean ofthe absolute fecal chymotrypsin levels at week 12 are close to the “normal old” of chymotrypsin (12.6 in frozen stool) regardless of the increase in CHO intake over the course of the trial. The subjects treated with o continue to remain abnormal with respect to their level of chymotrypsin at week 12 regardless of increase in the amount ofCHO change over the course ofthe trial.

Figure 49 illustrates the fecal chymotrypsin change as a ﬁanction of carbohydrate intake change: there is a signiﬁcant difference n subjects who are ed with Chymotrypsin in the trial (i.e., ts administered Formulation 1) and subjects administered a placebo. This change occurs regardless of the amount of increase in carbohydrate intake over the course of the 12 week trial. Importantly, food intake, in this case CHO, did not induce natural chymotrypsin into subjects on placebo. It is likely that the carbohydrate changes during the trial as subjects administered Formulation 1 and placebo could have an increase in carbohydrate intake due to ing requirements for calories.

Figure 50 illustrates the Vitamin K intake change as a ﬁanction of fecal chymotrypsin at week 12. The Vitamin K intake levels in subjects administered placebo ﬂuctuate between -3 and 1.5 g at week 12. For subjects administered placebo who are in the normal range for fecal chymotrypsin at week 12, their Vitamin K intake ranges from 0 to -3 g. For subjects on Formulation l, the Vitamin K intake ranged from -0.l to 4 g. For subjects in the normal range ofFCT at week 12, their n K intake ranged from 3.5 to 4 grams. Starting at 8.0 U/g of activity of rypsin the range went from 0.8 to 4.

Figure 51 illustrates the alpha carotene change as a ﬁanction of fecal chymotrypsin at week 12.

Figure 52 illustrates the Conners Parent Content Hyperactivity Change as a Function of Carbohydrate Intake Change. The subjects on Formulation 1 had a greater ement change (negative “-” is improvement) on parent content hyperactivity scores compared to subjects on placebo. Additionally aﬁer a 20 g+ change in CHO intake, the change in Formulation 1 ts s constant, and the change in placebo subjects demonstrates a worsening of ms (positive “+” change on the .

] Figure 53 illustrates the Conners hyperactivity change as a ﬁanction of carbohydrate intake change at week 12.

Figure 54 illustrates the Conners inattention change as a ﬁanction of carbohydrate intake change.

Figure 55 illustrates the Conners conduct disorder change as a ﬁanction of fecal chymotrypsin at week 12.

Figure 56 illustrates the Conners tional deﬁant change as a ﬁanction of fecal chymotrypsin at week 12.

] Figure 57 illustrates the PPVT mean growth score change as a ﬁanction of fecal chymotrypsin at week 12.

Figure 58 illustrates the EVT mean growth score change as a ﬁanction of fecal chymotrypsin change at week 12.

DETAILED DESCRIPTION OF THE INVENTION Digestive enzymes are produced by the salivary glands, glands in the stomach, the pancreas, and glands in the small ines. For example, ive enzymes produced by the pancreas and secreted into the stomach and small intestine aid digestion. Digestive enzymes produced by the pancreas are secreted into the duodenum, or upper segment ofthe small intestine, where the pH needs to be approximately 5 to 6.6, whereby the enzymes can assist in the digestion of food components, including carbohydrates, lipids, proteins and nucleic acids and other food components. When food is consumed, it is exposed to a highly acidic environment in the stomach (pH 1-2). Aﬁer the partial digestion of the food occurs in the stomach the food passes into the proximal portion of the small intestine (duodenum). The presence of the food in the duodenum (mechanoreceptors) and the very acidic pH (1-2) signals to the pancreas to secrete the enzymes precursors (pro-enzymes also known as zymogens) along with bicarbonate ions.

The food is then exposed to the pancreatic secreted proenzymes along with bicarbonate ions, which turns the pH of the duodenal environment ﬁom a pH 1-2 to a pH 5-6.5. The proezymes are then activated ﬁom their inactive zymogen state to an active form (for example: trypsinogen is converted to trypsin, and rypsinogen is converted into the active chymotrypsin).

Digestive enzymes have been stered to mammals to treat enzyme deﬁciencies caused by ions affecting the pancreas, such as atitis and pancreatic enzyme ncy or insufﬁciency. Pancreatic enzymes administered to humans are commonly ine origin. Manufacturers of enzyme preparations have also used enteric coatings for compositions in subjects who require administration of lipases. Orally administered enzyme preparations which are comprised ofpre ted s are exposed to highly acidic conditions in the stomach, with a pH of around pH 1-2, as well as gastric proteases which denature and e the enzymes; especially the lipase portion of the enzyme mixture which is highly sensitive to water air and proteases degradation.

The preparations for lipase delivery have used enteric coatings containing, for example, hypromellose ate, dimethicone 1000, and dibutyl phthalate. n methods for coating sensitive bioactive substances have been described. US. Patent No. 6,261,613 to Narayanaswamy et al. discloses particles that can contain yeast, coated in a shell of a fat in a beta prime form (z'.e. , triglyceride crystals having a blocky symmetry). The coating material can r contain emulsiﬁers such as those found in hydrogenated ble oil. However, the coating only allows release of the yeast in a limited temperature range of about 40° C to about 55° C US. Pat. No. 6,251,478 to Paciﬁco et al. ses certain sensitive nces ing certain bioactive compounds encapsulated in a lipid material.

Described herein are embodiments for coated digestive enzyme preparations, pharmaceutical compositions and enzyme delivery systems comprising coated digestive enzyme preparations, which are useful in the treatment of subjects with autism, ADD, ADHD, other neurological and behavioral diseases or conditions.

Autism or autistic disorder is the most common condition in a group of developmental disorders known as the autistic spectrum disorders (ASDs). Autism is characterized by impaired social interaction, problems with verbal and nonverbal communication, and unusual, repetitive, or ly limited activities and interests. Other ASDs include Asperger syndrome, Rett syndrome, childhood egrative disorder, and pervasive developmental disorder not otherwise speciﬁed (usually referred to as PDDNOS ). It has been estimated that l in 88 subjects in the US have some form of autism.

The numbers worldwide vary from 1 in 32 to 2—3 in 1000. In one embodiment, the compositions described herein are able to treat both the core and the non-core symptoms of autism.

] The re symptoms of autism include the following: seizure disorders, sensory integration disorders, gastrointestinal disorders, proprioceptive disorders such as balance and other issues.

] Attention deﬁcit-hyperactivity disorder (ADHD) is a neurobehavioral disorder that affects 3-5 percent of all subjects in the US. A similar incidence can be found world-wide. ADHD interferes with a person’s ability to stay on a task and to se propriate inhibition (cognitive alone or both cognitive and behavioral).

Some ofthe diagnostic signs ofADHD include failure to listen to instructions, inability to organize oneself and school work, ﬁdgeting with hands and feet, talking too much, abandoning projects, chores and leaving homework unﬁnished, and having trouble paying attention to and responding to details. Dysgraphia and disinhibition are ﬁlrther symptoms found in ADHD. There are several types ofADHD: a predominantly inattentive subtype, a inantly hyperactive-impulsive subtype, and a combined subtype. ADHD is usually diagnosed in ood, although the condition can continue into the adult years.

ADHD is presently comprised ofwhat was at one time known as Attention Deﬁcit er (ADD) and Attention Deﬁcit hyperactivity disorder (ADHD).

Criteria of Neurological or Mental Health Disorders The American Psychiatric Association's Diagnostic and Statistical Manual- IV, Text on (DSM-IV-TR) 1 provides standardized criteria to help diagnose Autistic Spectrum Disorders .

Psychiatric Diagnoses are rized by the Diagnostic and Statistical Manual of Mental Disorders, 4th. Edition. Better known as the DSM-IV, the manual is published by the an Psychiatric Association and covers all mental health disorders for both subjects and adults. It also lists known causes of these ers, statistics in terms of gender, age at onset, and prognosis as well as some research concerning the optimal treatment approaches.

Mental Health Professionals use this manual when working with subjects in order to better tand their illness and potential treatment and to help 3rd party payers (e.g., insurance) understand the needs of a subject. The book is typically considered the ‘bible’ for any professional who makes psychiatric diagnoses in the United States and many other countries. Much ofthe diagnostic information on these pages is gathered from the DSM IV.

The DSM IV is hed by the American Psychiatric Association. Much ofthe information from the Psychiatric Disorders pages is summarized from the pages of this text. Should any questions arise concerning incongruencies or inaccurate information, you should always default to the DSM as the ultimate guide to mental disorders.

The DSM uses a xial or imensional approach to diagnosing because rarely do other factors in a person's life not impact their mental health.

] Pervasive development disorders can be classiﬁed under the DSM-IV-TR classification as an autistic er, Asperger’s Disorder, PDD-NOS (including atypical autism), Rett’s Disorder and Childhood Disintegrative Disorder. The mental health ity is presently poised to convert their classiﬁcations of all mental health diagnostic criteria from the DSM-IV to the DSM-V. Both are outlined below. The DSM- V criteria are inclusive ofPDD-NOS and Asperger’s disorder, and also include sensory integration dysﬁlnction as a part for the diagnostic criteria.

DSM-IVDz'agnostl'c Criteriafor Autism Spectrum Disorder A subject must meet criteria A, B, C and D: ] A. Persistent ts in social communication and social ction across contexts, not accounted for by l developmental delays, and manifest by all 3 of the following: A1) Deﬁcits in social-emotional reciprocity; ranging from abnormal social approach and failure ofnormal back and forth conversation through reduced sharing of interests, emotions and affect and response to total lack of initiation of social ction; A2) Deﬁcits in nonverbal communicative behaviors used for social interaction; ranging from poorly integrated- verbal and non-verbal communication, h abnormalities in eye contact and body-language, or deficits in understanding and use ofnon-verbal communication, to total lack of facial expression or gestures; and A3) Deﬁcits in developing and ining relationships, appropriate to developmental level (beyond those with caregivers); ranging from difﬁculties in sharing imaginative play and in making friends to an apparent absence of interest in people.

B. Restricted, repetitive patterns of behavior, interest, or activities as manifested by at least two of the following: B1) Stereotyped or repetitive speech, motor nts, or use of objects (such as simple motor stereotypes, echolalia, repetitive use of objects or idiosyncratic phrases).

B2) Excessive adherence to routines, ritualized patterns of verbal or nonverbal behavior, or excessive resistance to change (such as motoric rituals, insistence on same route or food, repetitive questioning or e distress at small changes).

B3) Highly restricted, ﬁxated interests that are abnormal in intensity of focus (e.g., strong attachment to or preoccupation with unusual objects, excessively circumscribed or perseverative interests).

B4) Hyper- or hypo-reactivity to sensory input or unusual interest in sensory aspects of environment (e.g., apparent indifference to pain/heat/cold, adverse response to speciﬁc sounds or textures, excessive smelling or touching of objects, fascination with lights or spinning objects).

C. Symptoms must be present in early childhood (but may not become ﬁally manifest until social demands exceed limited ties).

D. Symptoms together limit and impair everyday ﬁlnctioning.

DSM-IVDiagnostic Criteriafor ive pmental Disorder Not ise Speciﬁed (Including Atypical Autism) This category should be used when there is a severe and pervasive ment in the development ofreciprocal social interaction associated with impairment in either verbal or nonverbal ication skills or with the presence of typed behavior, interests, and activities, but the criteria are not met for a speciﬁc Pervasive Developmental Disorder, phrenia, Schizotypal Personality Disorder, or Avoidant Personality Disorder. For example, this category es "atypical autism" - presentations that do not meet the criteria for Autistic Disorder because of late age at onset, atypical symptomatology, or reshold symptomatology, or all of these.

DSM-IVDiagnostic Criteriafor Rett's Disorder A. All of the following: A1) ntly normal prenatal and perinatal development; A2) apparently normal motor development through the ﬁrst 5 months after birth; and A3) normal head circumference at birth.

B. Onset of all of the following after the period ofnormal development: B1) deceleration of head growth between ages 5 and 48 months; ] B2) loss iously acquired purposeful hand skills n 5 and 30 months with the subsequent development of stereotyped hand movements (e.g., hand- wringing or hand washing); B3) loss of social engagement early in the course ( although often social interaction develops later); B4) appearance ofpoorly coordinated gait or trunk movements; and B5) severely impaired expressive and receptive language development with severe psychomotor retardation.

DSM-IVDz'agnostl'c Criteriafor Childhood Disintegrative er A. Apparently normal development for at least the ﬁrst 2 years after birth as manifested by the presence of age-appropriate verbal and nonverbal communication, social relationships, play, and ve behavior.

B. Clinically signiﬁcant loss ofpreviously acquired skills (before age 10 years) in at least two of the following areas: ] B1) expressive or receptive language; B2) social skills or adaptive behavior; B3) bowel or bladder control; B4) play; and B5) motor skills.

C. Abnormalities of ﬁanctioning in at least two of the following areas: C1) qualitative impairment in social interaction (e.g., impairment in nonverbal behaviors, failure to develop peer relationships, lack of social or emotional reciprocity); C2) qualitative impairments in communication (e.g., delay or lack of spoken ge, inability to initiate or sustain a conversation, stereotyped and repetitive use of ge, lack of varied make-believe play); and ] C3) restricted, tive, and stereotyped patterns of behavior, interest, and activities, including motor stereotypes and mannerisms. 2013/020183 D. The disturbance is not better accounted for by another speciﬁc Pervasive Developmental Disorder or by Schizophrenia Diagnostic Criteriafor Asperger's Disorder A. Qualitative impairment in social interaction, as manifested by at least two ofthe following: A1) marked ment in the use of multiple bal ors such as eye-to eye gaze, facial expression, body postures, and gestures to regulate social interaction; A2) failure to develop peer relationships riate to developmental level; A3) a lack of spontaneous seeking to share enjoyment, interests, or achievements with other people (6.g. a lack of g, bringing, or ng out , by objects of interest to other people); and A4) lack of social or emotional reciprocity.

B. Restricted repetitive and typed patterns of behavior, interests and activities, as manifested by at least one of the following: B1) encompassing preoccupation with one or more stereotyped and restricted patterns of interest that is abnormal either in intensity of focus; B2) apparently inﬂexible adherence to speciﬁc, nonﬁlnctional es or rituals; B3) stereotyped and repetitive motor mannerisms (e.g., hand or ﬁnger ﬂapping or twisting, or complex whole-body movements); and B4) persistent preoccupation with parts of objects.

C. The disturbance causes clinically signiﬁcant impairment in social, occupational, or other important areas of ﬁlnctioning.

D. There is no clinically signiﬁcant general delay in language (e.g., single words used by age 2 years, communicative phrases used by age 3 years).

E. There is no clinically cant delay in cognitive development or in the development of age-appropriate self-help , ve behavior (other than in social interaction), and curiosity about the nment in childhood.

F. Criteria are not met for another speciﬁc Pervasive Developmental Disorder or Schizophrenia. onal tests which may be used to assess subjects include, but are not limited to: EVT, PPVT, ADI-R, DSM-IV, SCQ, Block food screener, ABC checklist, and the s test.

DSM-VDiagnostic Criteriafor ic Disorder A. Six or more items from (1), (2), and (3), with at least two from (1), and one each from (2) and (3): A1) qualitative impairment in social interaction, as manifested by at least two ofthe following: Ala) marked impairment in the use of multiple nonverbal behaviors such as eye-to-eye gaze, facial expression, body postures, and gestures to regulate social interaction; Alb) failure to develop peer relationships riate to developmental level; Alc) a lack of spontaneous seeking to share enjoyment, interests, or achievements with other people (6.g. a lack of showing, bringing, or pointing out , by objects of interest); and ] Ald) lack of social or emotional reciprocity.

A2) qualitative impairments in communication as manifested by at least one ofthe following: A2a) delay in, or total lack of, the development of spoken language (not anied by an attempt to compensate through alternative modes of ication such as gesture or mime); A2b) in subjects with adequate speech, marked impairment in the ability to initiate or sustain a conversation with others; A2c) stereotyped and repetitive use of ge or idiosyncratic language; A2d) lack of varied, spontaneous make-believe play or social imitative play appropriate to developmental level.

A3) restricted tive and stereotyped patterns of behavior, interests, and activities, as manifested by at least one of the following: A3a) encompassing upation with one or more stereotyped and cted patterns of interest that is abnormal either in intensity or focus; A3b) apparently inﬂexible adherence to speciﬁc, nonﬁlnctional routines or rituals; A30) stereotyped and tive motor manners (e.g, hand or ﬁnger g or twisting, or complex whole-body movements); and A3d) tent preoccupation with parts of objects.

B. Delays or abnormal ﬁlnctioning in at least one of the following areas, with onset prior to age 3 years: (1) social ction, (2) language as used in social communication, or (3) symbolic or imaginative play.

C. The disturbance is not better accounted for by Rett’s Disorder or Childhood Disintegrative Disorder.

Further consideration with respect to levels of severity ofASD can be found in the following table: Severity Level for ASD Social Communication Restricted Interests and Repetitive behaviors Level 3 Severe deﬁcits in verbal and Preoccupations, ﬁxated non-verbal communication rituals and/or repetitive Requiring very skills cause severe behaviors ly substantial support impairments in oning; interfere with ﬁlnctioning very limited initiation of in all spheres. Marked social interactions and ss when rituals or minimal response to social routines are interrupted; overtures from . very difﬁcult to redirect from ﬁxated interest or returns to it quickly.

Level 2 Marked deﬁcits in verbal and RRBs and/or other rbal social preoccupations or ﬁxated ing substantial communication skills; social interests appear frequently support ments apparent even enough to be obvious to with supports in place; the casual observers and d initiation of social interfere with ﬁlnctioning interactions and reduced or in a variety of contexts. abnormal response to social Distress or ﬁustration is overtures from others. apparent when RRBs are interrupted; difﬁcult to redirect from ﬁxated interest.

Level 1 Without supports in place, Rituals and repetitive deﬁcits in social behaviors (RRBs) cause Requiring support communication cause signiﬁcant interference Severity Level for ASD Social Communication Restricted Interests and Repetitive behaviors noticeable impairments. Has with ﬁlnctioning in one or difﬁculty initiating social more contexts. Resists interactions and attempts by others to demonstrates clear examples interrupt RRBS or to be of atypical or unsuccessful redirected from ﬁxated responses to social overtures interest. of others. May appear to have decreased interest in social ctions.

Diagnostic Testing and Assessment ofAutism Severity Diagnostic Testing Assessment tools can be utilized to diagnose the presence of autism as well as the severity of . The two most comprehensive testing methods are the ADOS and the Autism Diagnostic Interview-Revised (ADI-R). Both are comprehensive and considered a c diagnostic tool for the ination of the ty of autism. ADI-R has the added beneﬁt of necessitating ng for those who administer the test. That training is rdized, which allows for the rdization across multiple clinical sites for example in a clinical trial Autism Diagnostic Interview-Revised (ADI-R) {00451} The ADI-R test may be used in the methods described herein to assess autism in subjects and adults and has been described by Anne Le r, Catherine Lord, and Michael Rutter, (Western Psychological Services, 2003).

ESEMSZE The Autism Diagnostic Interview-Revised (ADI-R) is a clinical diagnostic instrument for assessing autism in subjects and adults. The ADI-R es a diagnostic algorithm for autism as bed in both the lCD-lO and . The ment focuses on behavior in three main areas: qualities of reciprocal social interaction; communication and language; and restricted and repetitive, stereotyped interests and behaviors. The ADI-R is appropriate for subjects and adults with mental ages from about 18 months and above.

The ADI-R (Lord et al., 1994; Rutter, LeCouteur, et al., 2003) is a comprehensive parent interview that probes for symptoms of autism. It is administered by a trained clinician using a semi-structured interview format. The research or long version ofthe ADI-R requires approximately 3 hours (hr) to administer and score, The ADI-R elicits information from the parent on current or and developmental y. It is closely linked to the diagnostic criteria set forth in the DSM- IV-TR and International Classiﬁcation of Diseases-10. The ADI-R is a very l tool, but it does have some limitations. It is not ive to differences among subjects with mental ages below 20 months or IQs below 20 (Cox et al., 1999; Lord, 1995) and is not advised for use with such subjects. In particular, its sensitivity to the milder ASDs (AS and PDDNOS) is low at age 2, but good by 3.5 years. It is not designed to assess change through repeated administrations and is best suited to conﬁrm the initial diagnosis of autism d et al., 2000), Finally, and perhaps most important, it is labor intensive and requires more administration time than many practitioners may be able to allot.

} The ADI-R is a standardized, semi-structured clinical review for caregivers of subjects and adults. The interview contains 93 items and focuses on behaviors in three content areas or domains: y of social interaction (e.g., emotional sharing, offering and seeking comfort, social smiling and responding to other subjects); communication and language (e.g., stereotyped utterances, pronoun reversal, social usage of language); and repetitive, restricted and stereotyped interests and behavior (e.g., unusual preoccupations, hand and ﬁnger mannerisms, unusual sensory interests). The measure also includes other items relevant for treatment planning, such as self-injury and over-activity. Responses are scored by the clinician based on the caregivers description ofthe child's behavior. Questions are organized around content area, and deﬁnitions of all behavioral items are provided. Within the area of ication, for example, “Delay or total lack of language not compensated by gesture” is r broken down into speciﬁc behavioral items: pointing to express interest, conventional gestures, head nodding, and head shaking. Similarly, within the area of Reciprocal Social Interaction, lack of socio- emotional ocity and modulation to t include the following behaviors: use of other's body, offering comfort, inappropriate facial expressions, quality of social overtures, and appropriateness of social response. {004%} The interview starts with an introductory question followed by questions about a subject's early development. The next 41 questions cover verbal and nonverbal communication. Questions 50 through 66 ask about social development and play. The next 13 questions deal with interests and behaviors. The ﬁnal 14 ons ask about “general behavior,” ing questions about memory skills, motor , over-activity and fainting. 2013/020183 [0045?] The ADI-R interview generates scores in each of the three t areas (i.e., communication and language, social interaction, and restricted, repetitive behaviors).

Elevated scores indicate problematic behavior in a ular area. Scores are based on the clinician's judgment following the caregiver's report of the child's behavior and development. For each item, the clinician gives a score ranging from 0 to 3. A score of 0 is given when “behavior ofthe type ed in the coding is not present”; a score of l is given when “behavior ofthe type speciﬁed is present in an abnormal form, but not sufﬁciently severe or frequent to meet the criteria for a 2”; a score of 2 indicates “deﬁnite abnormal behavior” g the criteria speciﬁed; and a score of 3 is reserved for “extreme severity” of the speciﬁed behavior. (The interviewers of the e recode 3 as a 2 in computing the algorithm.) There are also scores of 7 (“deﬁnite abnormality in the general area of the coding, but not of the type speciﬁed”), 8 (“not able”), and 9 (“not known or not asked”) given under certain circumstances, which all are converted to 0 in ing the algorithm.

This interviewer-based instrument requires substantial training in administration and scoring. A highly trained clinician can administer the ADI-R to the parent of a 3- or 4-year old suspected of autism in approximately 90 minutes. The interview may take at longer when administered to parents of older subjects or adults. ng workshops are available in the United States as well as internationally.

The ADI-R and related materials are available from Western Psychological Services. rater and test-retest reliability, as well as al validity, have been demonstrated for the ADI-R. A detailed graphy (with abstracts) describing the psychometric properties ofthe ADI-R can be found on the University of Michigan Autism Communication and Disorders Center website.

The Social Communication Questionnaire The Social Communication Questionnaire (SCQ; Rutter, Bailey, & Lord, 2003), previously known as the Autism Screening Questionnaire (ASQ), was initially designed as a companion screening measure for the Autism Diagnostic Interview-Revised (ADI-R; Rutter, Le Couteur & Lord). The SCQ is a parent/caregiver dimensional e ofASD symptomatology appropriate for subjects of any chronological age older than four years. It can be completed by the informant in less than 10 minutes.

The Social Communication onnaire (is a parent-report questionnaire based on the ADI-R, It contains many ofthe same questions included on the ADI-R algorithm, presented in a briefer, yes/no format that parents can complete on their own. 2013/020183 The primary standardization data for the SCQ was obtained from a sample of200 subjects who had ipated in previous studies ofASD. The SCQ is available in two forms: Lifetime and Current; each with 40 questions presented in a yes or no format.

Scores on the questionnaire provide an index of symptom severity and indicate the likelihood that a subject has an ASD. Questions include items in the reciprocal social interaction domain (e.g., “Does she/he have any particular friends or best friend?”), the communication domain (e.g., “Can you have a to and fro ‘conversation’ with him/her that involves administered turns or building on what you have said?”) and the restricted, repetitive, and stereotyped patterns ofbehavior domain (e.g., Has she/he ever seemed to be more interested in parts of a toy or an object [e.g., ng the wheels of a car], rather than using the object as intended?”).

Compared to other screening measures, the SCQ has consistently demonstrated its effectiveness in predicting ASD versus non-ASD status in multiple studies. The scale has been found to have good discriminant validity and utility as an efﬁcient screener for at-risk groups of school-age ts. A threshold raw score of >15 is recommended to minimize the risk of false negatives and te the need for a hensive evaluation. Comparing autism to other diagnoses (excluding mental retardation), this threshold score resulted in a sensitivity value of .96 and a specificity value of .80 in a large population of subjects with autism and other pmental disorders. The positive tive value was .93 with this cutoff The authors recommend using different cut-off scores for different purposes and populations (e.g., a cut-off of 22 when differentiating autism from other ASDs and a cut-off of 15 when differentiating ASD from non-ASD). Several s (Allen et al., 2007; Eaves et al., 2006) have suggested that a cut-off of 11 may be more clinically useful s & lier, 2010).

The SCQ is one ofthe most researched ofthe ASD-specific evaluation tools and can be recommended for screening and as part of comprehensive developmental assessment for ASD (Norris & Lecavalier, 2010; Wilkinson, 2010, 2011). The SCQ is an efﬁcient screening instrument for identifying subjects with possible ASD for a more in- depth assessment. For clinical purposes, practitioners might consider a multistage assessment beginning with the SCQ, followed by a comprehensive developmental evaluation (Wilkinson, 2011). r, cut-off scores may need to be adjusted depending on the population in which it is used. The evidence also indicates that although the SCQ is riate for a wide age range, it is less effective when used with younger populations (e.g., subjects two to three years). It was designed for subjects above the age of four years, and seems to perform best with subjects over seven years of age.

Its agreement with the more labor-intensive ADI-R on diagnostic categorization is high (Bishop & Norbury, 2002), and it is thus an efficient way to obtain stic information or screen for autistic symptoms. There are two versions available: one for current behavior and one for lifetime behavior. The lifetime version is helpful for screening and diagnostic purposes, whereas the current n is more appropriate for assessment of change over time in a subject, A cutoff score of 15 differentiates between ASD and other diagnoses for subjects ages 4 years and older, s a cutoff of 22 minates subjects with ic disorder from those with other ASDs (PDDNOS or AS). Using these cutoffs, sensitivity of 0.85 and specificity of 0.75 have been ed in a large sample of subjects and adults with autism and other developmental disorders (Berumentetal, 1999).

DSM-IV and DSM-V criteria ADI-R, SCQ and ADOS, for example, are measures ofthe presence and, in some cases, the severity of autism. Those which look at severity such as ADI-R, ADOS and SCQ which measure severity cannot be utilized as outcome measures for test and retest of subjects with autism when administered an ention. Their use and validation are strictly relegated to diagnosis. There is no test re-test validation, and they are not designed to examine change seen in subjects with autism.

Behavioral assessments Behavioral testing can be utilized to e changes in subjects with autism who are administered an intervention. The pre test post test format is not able to be utilized with the diagnostic measures, but can be utilized with many of the behavioral ments.

Aberrant Behavior Checklist The Aberrant Behavior ist (ABC) scale is a standardized set of questions used for ing subjects and can be found, for e, published in the 1994 Slosson Educational Publications, Inc. (Aman et al.) and the assessment serves as the standard for assessing subjects. Behavioral attributes are rated as follows: 0 = not at all a problem; 1 = the behavior is a problem, but slight in decree; 2 = the problem is moderately serious; or 3 = the problem is severe in .

The s (subscales) of the ABC scale are as follows: (I) irritability, agitation, crying; (II) lethargy, social withdrawal; (III) stereotypic behavior; (IV) hyperactivity, noncompliance; and (V) inappropriate speech. A series of ons is asked with t to each of the scales and each is rated 0-3.

Three scales have signiﬁcant number of data points and validated: Irritability / Agitation ore) Primary; Lethargy/ Social awal (core) Secondary; and ctivity (non-core, high morbidity). Two minor scales are: Stereotypic Behavior and Inappropriate . The s of questions on each subscale are as follows: 1) Irritability, ion, crying (15 items); 2) Lethargy, social withdrawal (16 items); 3) Stereotypic behavior (7 items); 4) Hyperactivity, non- compliance (16 items); and 5) Inappropriate speech (4 items) The questions on the ABC test are as follows: 1. ively active at home, school, work or elsewhere 2. Injures self on purpose 3. Listless, sluggish, inactive 4 Aggressive to other subjects or adults (verbally or 0000 p—Ap—Ap—Ap—A NNNN 03030303 physically) . Seeks isolation from others $9909?) Meaningless, recurring body movements p-Ap-A Boisterous (inappropriately noisy and rough) Screams inappropriately Talks excessively lO. Temper tantrums/outbursts . Stereotyped or; abnormal, repetitive movements 12. Preoccupied; stares into space l3. Impulsive (acts without thinking) 14. Irritable and whiny . Restless, unable to sit still l6. Withdrawn; prefers solitary activities l7. Odd, bizarre in behavior l8. Disobedient; difficult to control b—KD—‘b—‘l—‘b—KD—‘b—‘l—‘b—KD—‘b—‘H 19. Yells at inappropriate times . Fixed facial expression/ lacks emotional responsiveness 21. Disturbs others 22. Repetitive speech p—Ap—Ap—Ap—A 23. Does nothing but sit and watch others p-A Uncooperative OOOOOOOOOOOOOOOOOOOO 24. NNNNNNNNNNNNNNNNNNNN 0303030303030303030303030303030303030303 . Depressed mood l 2 26. Resists any form ofphysical contact 27, Moves or rolls head back and forth repetitively 28. Does not pay attention to instructions 29. s must be met immediately . Isolates himself/herself from other ts or adults j—Ap—Ap—Ap—A 31. Disrupts group activities 32. Sits or stands in one position for a. long time 33. Talks to self loudly 34. Cries over minor annoyances and hurts j—Ap—Ap—Ap—A . Repetitive hand, body, or head movements p-A 36. Mood changes quickly 37. Unresponsive to structured activities (does not react) 0000000000000 NNNNNNNNNNNN WWWWWWWWWWWWW 38. Does not stay in seat (e. g., during lesson or training periods, meals, etc.) 39. Will not sit still for any length of time 40. Is difficult to reach, contact, or get through to 41. Cries and s inappropriately 42. Prefers to be alone 43. Does not try to icate by words or gestures b—‘ﬁ—‘b—‘b—KH 44. Easily distractible 45. Waves or shakes the extremities repeatedly 46. Repeats a word or phrase over and over D—t>—‘ 47. Stamps feet or bangs objects or slams doors 48. Constantly runs or jumps around the room 49. Rocks body back and forth repeatedly 50. Deliberately hurts himself/herself 51. Pays no attention when spoken to 52. Does physical ce to self 53. Inactive, never moves spontaneously 54. Tends to be excessively active b—‘ﬁ—‘b—‘b—KD—‘ﬁ—‘b—‘b—K 55. Responds negatively to affection p-A 56. Deliberately ignores directions OOOOOOOOOOOOOOOOOOO NNNNNNNNNNNNN WWWWWWWWWWWWWWWWWWW 57. Has temper outbursts or tantrums WO 03746 2013/020183 when he/she does not get own way 58. Shows few social reactions to others The ABC has been utilized in autism drug clinical trials because it has the characteristics of validity, reliability and drug sensitivity. All three are necessary to make the ABC useable as an outcome measure for clinical trials for drugs for . It is a predictor of maladaptive behavior. ive psychometric assessment ofthe ABC has indicated that its subscales have high internal consistency, adequate reliability, and established validity. 0.94 in the original development study. Generally, other studies have conﬁrmed this range of internal consistencies. However, some studies have found internal consistencies as low as 0.19 (Freund, teacher form).

Test-retest: The original development study reported test-retest reliabilities of 0.96-0.99. However, the subsequent studies failed to validate these ﬁndings. Generally, have been fairly good, ranging from 0.50-0.67 (Freund, teacher form) to 0.80-0.95 (Freund, parent form).

Inter-rater: The original development study reported inter-rater reliabilities of 0. 17-090, with a mean of 0.60. Subsequent s have found a wide variability of inter-rater ilities, ranging from 0.12 to 0.95 (both in Schroeder).

Validity There has been extensive validation of the 5-factor structure. The original development study found that the ABC demonstrated moderate discriminative validity with a number of instruments, as well as convergent validity with oral observation reports. It also demonstrated te predictive ty. Subsequent studies have provided ﬁarther evidence of predictive, gent and discriminative validities.

The EVT-2 test The EVT-2 test builds on the strength of the EVT in that is brief and easy to administer; the EVT-2 assessment has been ed to coordinate with the PPVTTM-4 (Peabody Picture Vocabulary Test, Fourth Edition) test. Together, these tools give provide a comprehensive system for comparing receptive and expressive vocabulary.

Unlike some other measures ofvocabulary, the EVT-2 es two equivalent forms ofthe test which contain different vocabulary items—helping ensure a subject has not “learned” the test. One form can be used prior to intervention to assess subjects’ vocabulary knowledge and the alternative form can be used for re-testing to evaluate and document progress. EVT-2 also includes a unique Growth Scale Value (GSV) which is ive to small changes over time. Users & Applications The EVT-2 test is individually administered and norm-referenced. It meets the needs of a wide variety of professionals to help: (1) Quickly assess expressive vocabulary with a test that requires no reading or writing; (2) Evaluate English Language Learners’ (ELL) vocabulary acquisition as a ﬂexible measure of their English word knowledge; (3) Make comparisons with ive vocabulary to pinpoint a student’s ths/weaknesses and identify potential word retrieval concerns; (4) Move immediately into evidence-based interventions using those embedded directly into and linked into the ASSIST software (SAS; www.sas.com/products/assist/index.html); (5) Assess oral expression as a foundation of writing ; and (5) Measure progress using one or both parallel forms.

] Features & Beneﬁts and beneﬁts ofthe EVT-2 test include, for example, two parallel forms for easier progress monitoring; cal administration and scoring procedures to the EVT; broader and more mixed use of labeling and synonym item types; ﬁve levels of diagnostic analysis; and new Growth Scale Value (GSV) for measuring progress over time.

Developed over a ﬁve-year period, the EVT-2 test was co-normed along with the PPVT-4 test with a national sample of subjects ranging in age from 2:6—90+.

More than 5,500 subjects were tested; data from approximately 3,500 subjects were used for the ive scores. The remaining data contributed to the validation studies. The sample was y controlled and was matched to the US. Census on gender, race/ ethnicity, , socioeconomic status (SES), and clinical diagnosis or special education ent. The EVT-2 test provides extremely reliable scores, with reliability coefﬁcients in the 0.90s for almost every age or grade. Additionally, the PPVT-4 test offers many enhancements to a vocabulary assessment that has been well respected for 50 years. This latest edition has been co-normed with the sive Vocabulary Test, Second Edition (EVTTM-Z), allowing for direct isons between receptive and expressive lary performance.

The PPVT-2 test Unlike some other measures ofvocabulary, the PPVT-2 supplies two equivalent forms ofthe test which contain different lary items, thereby helping ensure a subject has not “learned” the test. One form can be used prior to intervention to assess subjects’ vocabulary knowledge and the alternative form can be used for re-testing to evaluate and document progress. PPVT-2 also includes a unique Growth Scale Value (GSV) which is sensitive to small changes over time.

The PPVT-4 test is individually administered and norm-referenced. It may be used to y evaluate receptive vocabulary with a test that requires no reading or writing; monitor progress using two parallel forms; directly compare ive and expressive vocabulary when you also administer the EVT-2; move immediately into evidence-based interventions using those embedded directly into and linked into the ASSIST software; and meet ines for universal ing, identifying strengths and weaknesses, and diagnostic testing in an RTI environment In normally developing subjects the EVT and the PPVT should demonstrate similar growth. The growth scales seen over a 12 month period should keep pace with one another. In the case of neurologically or otherwise impaired subjects the scales will often not keep pace with one r.

The Connors test Changes in hyperactivity can be ed in the Conners’ 3- which is the Gold Standard for diagnosing as well as ing ished medications for Attention Deﬁcit and Attention Deﬁcit Hyperactivity Disorders. s’ 3 can be administered according to conventional methods and scored ing the T-score ines.

Attributes that are assessed include: restless or overactive behavior; excitability and impulsiveness; failing to ﬁnish tasks; inattentiveness and ease of distraction; temper outbursts; ﬁdgeting; disturbances of other subjects; demands to be met immediately and ease of frustration; ease and frequency of crying; and rapid and drastic mood changes.

Each attribute is scored on a scale of 0-3 where 0 = never, seldom; l = occasionally; 2 = often, quite a bit; and 3 = very often; very frequent.

Block Food Screenersfor Ages 2-1 7 These ers are designed to assess subjects's intake by food group, with outcomes measured in number of servings. One version asks about food eaten “yesterday,” and a second version about food eaten “last week.” The focus of these tools is on intake of fruit and fruit juices, vegetables, potatoes (including French fries), whole WO 03746 grains, meat/poultry/f1sh, dairy, legumes, saturated fat, “added sugars” (in sweetened s, soft drinks, and sweets), glycemic load and glycemic index. A secondary analysis produces estimates for intake of sugary beverages (both kcal and frequency). Individual portion sizes are asked. This questionnaire was designed for self-administration by subjects with the assistance of parent or caregiver, as needed.

The block food screener and block food screener last week have been utilized in clinical trials as well as by the USDA to examine food intake in s tions including subjects.

The tests have been ted and have excellent internal and external validity. The questionnaires are machine scored, and the intake is determined through a series of questions that have been designed to look at food types as well as portions to determine the intake of nutrients.

Enzyme Preparations and Uses Thereof Digestive enzymes to be used in the compositions and s described herein e, for e, pancreatic enzymes. There are two types reatic s which have U.S.P. designations: pancreatin and pancrealipase. atin is a substance containing enzymes, principally amylase, lipase, and protease, ed from the pancreas of the hog Sus scrofa Linne var. domesticus Gray (Fam. Suidae) or of the ox Bos Taurus Linne (Fam. Bocidae). Pancreatin contains, in each mg, not less than 25 USP units of amylase activity, not less than 2 USP units of lipase activity, and not less than 25 USP ofprotease activity. More information on Pancreatin is provided in Example 1 below. In contrast, pancrealipase USP refers to a cream-colored, amorphous powder, having a faint, characteristic (meaty), but not offensive odor, which contains Lipase in an amount of not less than 24 USP Units/mg; Protease in an amount ofnot less than 100 USP Units/mg; and Amylase in an amount ofnot less than 100 USP Units/mg; with not more than 5% fat and not more than 5% loss on drying.

Enzyme preparations with non-lipid enteric gs have been used to deliver lipases in subjects requiring administration of lipases to subjects in need of enzyme treatment. In addition, Fallon has bed certain methods and enzyme compositions for use in treating subjects and other subjects, with autism, ADD, ADHD, and other neurological diseases or conditions, for example, US. Patent Nos. 7,138,123, 6,660,831, 6,632,429; 6,534,063, hereby incorporated by reference as if set forth in fall herein.

The nature ofthe human digestive tract s challenges for the delivery of digestive s to subjects with neurological and behavioral conditions susceptible to treatment with digestive enzymes. Multiple temperature and pH changes over the course ofthe digestive tract make speciﬁc delivery a necessity and a challenge. For ce, pH as low as l is encountered in the stomach, but rapidly increases to a more basic pH of 5-6 in the proximal small intestine through the addition of bicarbonate ions secreted by the pancreas. For example, generally the pH in the stomach is approximately 1.2, the pH in the duodenum is about 5.0 to 6.5; the pH in the jejunum is about 6.8, and the pH is about 7.2 in the proximal ileum and about 7.5 in the distal ileum. The low pH in the stomach which changes rapidly to a more basic pH of 5-6 in the proximal small intestines, call for a speciﬁc delivery method depending upon where the enzyme is to be delivered.

For example, it was observed that subjects with autism who need ent with proteases beneﬁt from delivery e enzymes to the al small intestine.

Delivery of digestive enzymes can also be challenging due to the rapid degradation and denaturing of enzymes at ambient room temperature, as well as the enhanced degradation and denaturing that can occur with high temperature, re, humidity and/or exposure to light. Moisture and heat together can quickly destabilize enzymes, reducing their effectiveness, and shortening shelf life, leading to inaccurate dosing. Denaturization or destabilization of the enzymes can reduce their effectiveness by reducing the dose of active enzymes to less than the amount needed for ive treatment. Alternatively, attempting to compensate for the denaturization or destablization by increasing the dose to ensure an effective level of active enzyme, could risk an overdose or overﬁlling a capsule or other dosage form. To protect and stabilize the pancreatic/digestive enzymes from unfavorable conditions, such a penetration, decomposition, the pancreatic/digestive enzymes (core) can be coated or encapsulated in a continuous coating ning an emulsiﬁable lipid. In r , provided herein are new coated enzyme preparations with improved shelf life.

] In one embodiment, a composition provided herein contains the major proteases shown in Figure 15. Compositions provided herein are safe for administration to human subjects, including subjects. itions may be any form able for administration to a subject including, but not limited to particles, sprinkles, powder, tablets, mini-tablets, capsules, etc.

Manufacturers of enzyme preparations have used enteric coatings to deliver lipases in subjects ing administration of lipases. Because the porcine enzymes are delivered in a mixture ofproteases, s and amylases, and because these compositions for human consumption were prepared for lipase delivery, the uses ofthese enteric coatings, which e such substances as hypromellose phthalate, dimethicone 1000, and dibutyl phthalate, preclude delivery of proteases at the proper location in the digestive tract. All other enzyme preparations presently on the market contain at least one ofthese c coating substances and/or other additives in the preparation. Some additives that enable manufacturing, such as additives to improve ﬂow properties, can ﬁlrther risk t reactivity or ivity to the enzyme preparation.

] The use ofphalates which has been the state of the art for some time with respect to the delivery of enzymes which have been utilized to deliver lipases for pancreatitis. Phalates have been implicated in a number of diseases ing cancer and autism. The use of enteric coatings which are phalate derived were not utilized in this formulation due to these ial side effects.

FDA has issued a draft guidance with respect to the use of phalates and have requested that all pharmaceuticals which employ the use ates be re- formulated to exclude the use of phalates in all pharmaceutical preparations.

In one embodiment, a composition described includes a coated digestive enzyme preparation and/or composite, which, in some embodiments is an encapsulated pancreatic/digestive enzyme preparation. In other aspects, the invention includes enzyme delivery systems and pharmaceutical compositions comprising coated pancreatic/digestive enzyme preparations. These coated or encapsulated enzyme preparations contain cores comprising pancreatic or digestive enzyme particles, and a coating comprising an emulsif1able lipid.

The coatings in the digestive/pancreatic enzyme preparations create a r to degradation and denaturation, and allow more te levels of active enzymes to reach the treated subjects. The lipid coating of this invention provides a significant barrier to moisture, heat, ty and re to light by allowing for a physical barrier as well as one that prevents and or reduces hydrolysis. The coated enzyme preparations o less hydrolysis as a result of protection from moisture in the environment by the lipid coating. As a result of the present ion, pancreatic / digestive enzymes are provided which can tolerate storage conditions (e.g., re, heat, oxygen, etc.) for long periods oftime thus enabling extended shelf life. The coating of the encapsulated 2013/020183 enzyme preparation protects the enzyme from the environment and provides emulsif1cation in a solvent t detracting from the abrasion ance of the coating.

The invention thus ﬁarther relates to more stable enzyme preparations.

The coated enzyme preparations therefore reduce overﬁlling ofthe enzyme dosage, and enhance delivery of more accurate doses ofthe enzyme to subjects with autism, ADD, ADHD and other neurological or behavioral conditions or diseases susceptible to treatment with pancreatic or ive enzymes.

In addition, because subjects and other subjects with autism and other conditions often have multiple sensitivities to foods, additives, colorants and other carriers, excipients or substances used in drug formulations, it is a challenge to make an enzyme delivery system that avoids the use of allergens, and other carriers, excipients, extenders, nts, etc. that could potentially add to adverse symptoms or the morbidity of subjects. Furthermore, in very young ts, an enzyme ry system which allows ease and tolerability is paramount. A sachet ry system for these enzyme preparations has also heretofore not been ed.

It is another aspect of the present invention to use an enzyme preparation that is prepared without extenders nts, dyes, ﬂow enhancers and other additives to reduce the potential for allergens and other sensitivity reactions in subjects and other d subjects. It has been discovered that in some embodiments, the digestive s can surprisingly be encapsulated with a single lipid excipient to improve retention of enzyme actiVity, ease of administration, tolerability, and safety of administration, among other properties. It has been previously found that digestive enzyme particles containing lipases can be successfully encapsulated with coating consisting essentially of only hydrogenated soy oil.

In addition, porcine atic /digestive enzymes possess a significant odor and taste, similar to that of cured/smoked pork. This taste can be strong and offensive to some subjects stered enzyme replacement, and especially to subjects.

The addition of a lipid coating provides significant taste masking to the enzyme preparation, which allows for the tolerance of taste, as the lipid coating is odorless and tasteless. The use of this method of taste masking which does not involve the use of color, dyes, perﬁJmes, recipients, or other substances is preferable for the administration of medications, which have an unpleasant or undesirable taste and odor. In other embodiments, this invention relates to coated digestive enzyme preparations with improved taste and smell. 2013/020183 In some ments, the coatings on the ive enzyme particle cores are preferably continuous coatings. By “continuous,” it is meant that the pancreatic/digestive enzyme is uniformity protected. The continuous coating of the ﬁllly surrounds or encapsulates the pancreatic/digestive enzymes. The encapsulation provides protection of the pancreatic/digestive enzyme from conditions such as moisture, temperature, and conditions encountered during storage.

In addition, the encapsulation also provides controlled release of the pancreatic/digestive enzyme. The emulsiﬁcation properties ofthe coating in a solvent allows for controlled release of the enzyme in the gastrointestinal system, preferably the region ofthe GI tract where the enzymes are to be utilized. The coating ofthe ulated composite protects the enzyme from the environment and provides emulsiﬁcation in a solvent without detracting ﬁom the abrasion resistance of the coating.

For example, for ions ing ent with ses, the release of the protease portion of the enzymes is ary in the proximal small intestine, y necessitating a lipid encapsulation which has a dissolution proﬁle between 30-90 minutes. The dissolution proﬁle can also be about 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85 or 90 minutes. The dissolution proﬁle can also be enhanced by this method to included longer or shorter dissolution proﬁles. Dissolution proﬁles can be obtained using methods and conditions known to those of skill in the art. For example, dissolution proﬁles can be determined at various pH’s, including pH 1, 2, 3, 4, 5, 6, 7, 8, 9, 10.

The rate of release of the bioactive substance can also be controlled by the addition of additives as described below. When the preparations are exposed to a solvent, the solvent interacts with the molliﬁable lipid in the coating and results in emulsiﬁcation ofthe coating and release of the bioactive substance.

] “Encapsulate” as used herein means that the coating completely surrounds the pancreatic/digestive . In a population of ulated particles, encapsulated enzyme preparations can include inating or small portion of particles with a substantially continuous coating as long as the release proﬁles of the encapsulated les are not signiﬁcantly altered. A coated or encapsulated particle can contain one or more digestive enzyme particles enveloped in one coating to form one coated or encapsulated digestive enzyme particle in the coated or encapsulated digestive enzyme preparation.

Compositions described herein can be used for the treatment of neurological or behavioral disorders which have overlapping symptomotology. In addition to Autism and autism spectrum disorder ADD, ADHD, and the other behavioral or neurological conditions or diseases susceptible to treatment with pancreatic or digestive enzymes or with overlapping symptomotology By “susceptible to ent with atic or digestive enzymes” is meant that one or more symptoms ofthe disease or condition can be alleviated, treated, or d by administration of an effective amount ofpancreatic or ive enzymes.

There are often multiple co-morbid symptoms seen in behavioral or neurological conditions. For example, hyperactivity is 60% co-morbid in autism. Other symptoms which are oﬁen seen in multiple neurological conditions include seizure disorders. So seizures are a common occurrence in subjects with autism.

Compositions described herein can be used for the treatment of, for example, gastrointestinal issues (e.g., constipation and/or diarrhea) associated with the neurological disorder, seizures (e.g., “Grand Mal”, absence, myoclonic, tonic, clonic and/or atonic seizures), sensory issues (e.g., sight, sound, stimming, taste, touch and/or smell), speech issues such as expressive (e.g., stereotyped and tive) and/or receptive speech, socialization issues (e.g., lethargy, social ocity, non-verbal communication and/or peer onships), obsessive compulsive disorder issues such as obsession (e.g., thoughts, impulses and/or images) and compulsion (e.g., mental and/or behavioral), irritability, fragile X, hypersensory , ctivity issues, or a combination f It has been previously found that selected coated enzyme preparations can be made by coating digestive enzyme particles with lipids not previously used in coated digestive enzyme preparations. The unique es of emulsif1able lipids and enzymes can deliver certain ents of the pancreatic / digestive enzymes to ed locations and/or at selected times during transit of the GI tract. In some aspects are methods of delivering digestive enzymes to humans based upon dissolution proﬁles.

The emulsif1able lipid may be any lipid, lipid mixture, or blend of lipid and emulsifiers which emulsif1es when d to a solvent, and has a melting point which allows the lipid to be a solid at typical storage temperatures. The emulsiﬁable lipid can be a vegetable or animal derived-lipid. In some embodiments, the emulsiﬁable lipid consists essentially of, or comprises one or more monoglycerides, diglycerides or triglycerides, or other components including, for example, emulsifiers found in hydrogenated vegetable oils. In another embodiment the lipid is a non-polar lipid.

As used herein, animal and/or vegetable “derived” lipids can include fats and oils originating from plant or animal sources and/or s, and/or synthetically produced based on the structures of fats and oils originating from plant or animal sources.

Lipid material can be reﬁned, ted or puriﬁed by known chemical or mechanical processes. Certain fatty acids present in lipids, termed essential fatty acids, must be present in the mammalian diet. The lipid can, in some embodiments, comprise a Type I USP-National Formulary ble oil.

The digestive enzymes used in the t methods can be any combination of ive enzymes of a type produced by the as, including, but not limited to ive enzymes from a atic source or other sources. The enzymes are not limited to pancreatic enzymes ofporcine origin, but can be of other animal or plant origin as well as those which are synthetically derived. The digestive enzymes can be derived from mammalian sources such as porcine-derived digestive enzymes. The enzymes can include one or more enzymes, and can also be plant derived, synthetically derived, inantly produced in microbial, yeast, or mammalian cells, and can include a mixture of enzymes from one or more sources. Digestive enzymes can e, for example, one or more enzymes from more or more sources mixed together. This includes, for example, the addition of single ive enzymes to digestive enzymes derived from pancreatic sources in order to provide appropriate levels of c enzymes that provide more effective treatment for a selected disease or condition. One source of digestive enzymes can be obtained, for e, from Scientiﬁc Protein Laboratories.

The digestive enzyme can be, for example a pancreatic extract complex composition. In one embodiment, the digestive enzymes will comprise or consist essentially of 25 USP units/mg protease, 2 USP g lipase, and 25 USP Units/mg amylase. The term digestive enzyme can refer to one or more enzymes of a type produced by the pancreas.

The ive enzyme particles used as cores in the present invention include digestive enzyme particles where about 90% ofthe particles are n about #40 and #140 USSS mesh in size, or between about 105 to 425 um, or where at least about 75% ofthe particles are between about #40 and #80 mesh, or about 180 to 425 um in size. Particles between #40 and #140 mesh in size pass through #40 mesh but do not pass through #140 mesh. The coated or encapsulated digestive enzyme les in one embodiment ofthis invention can comprise less than about 35, 30, 25, 20, 15 or 10% of the particles which can be sieved through #100 mesh (150 um). In some embodiments, the term “non-aerosolizable” refers to a coated or encapsulated enzyme preparation where less than about 20% or less than about 15% of the particles can be sieved through #100 mesh (150 um). The encapsulated digestive enzyme preparation can be an encapsulated digestive enzyme composite where the digestive enzyme particles contain two or more enzymes.

The minimum amount ofpancreatic enzyme present in the core is at least about 5% active enzymes by weight ofthe coated enzyme ation, but in other embodiments can be at least about 30%, or at least about 50% by weight. The maximum amount ofpancreatic/digestive enzyme present in the composite is at most about 95% by weight, and in other embodiments at most about 90%, 85%, 80%, 75% or 70% ofthe coated enzyme preparation. In other embodiments, the amount ofpancreatic enzyme present in the ite is about 10%, 15%, 20%, 25%, 35%, 40%, 45%, 55%, 60%, 65%, 70%, 72.5%, 75%, 77.5%, 80%, 82.5%, 87.5%, or 92.5% by weight or anywhere in between.

] “At least about” or “at most about” a percentage (%) of enzyme can include equal to or about that % of enzyme. The term “about” includes equal to, and a range that takes into t experimental error in a given measurement. As used in connection with particle sizes, the term “about” can refer to plus or minus 10, 9, 8, 7, 6, 5, 4, 3, 2 or 1% or anywhere ween. As used in tion with % particles that can be sieved, the term “about” can refer to plus or minus 10, 9, 8, 7, 6, 5, 4, 3, 2 or 1% or anywhere ween.

The composition which contains the encapsulated digestive enzyme preparation or composite can be delivered as a sprinkle, powder, capsule, , pellet, caplet or other form. Packaging the encapsulated enzyme preparations in an enzyme delivery system that ﬁthher ses single dose sachet-housed sprinkle preparations allows for ease of delivery, and accurate dosing of the enzyme, by allowing a speciﬁc amount of enzyme to be delivered in each dosing. Allowing for speciﬁc unit dosing of an enzyme preparation which maintains the enzyme activity within speciﬁc stability parameters in an enhancement over other sprinkle formulations, which are , in a multi-unit dosing form that allows for air, moisture and heat to depredate and denature the enzyme preparation. In a preferred embodiment the powder or sachet is housed in a trilaminar foil pouch, or similar barrier to keep out moisture and to protect the enzyme preparation from adverse environmental s. The invention ﬁlrther relates to an improvement in stability due to a reduction in hydrolysis due to the lipid encapsulation.

Further, the lipid encapsulation methodology reduces the lization of the enzyme preparation that can be caustic to the child if inhaled through the lungs or the nose. In another embodiment, the invention includes delivery of digestive enzymes with ed safety of administration, by reducing the amount of aerosolization of the enzyme. The lipid ulation reduces aerosolization and the potential for caustic burn, aspiration, and/or aspiration pneumonias in ts and administrators of the enzyme ation, thereby reducing the potential for s in already compromised subjects, and leading to safer administration.

As used herein, the term “non-aerosolizable” will be used to refer to a coated or encapsulated enzyme preparation where substantially all of the particles are large enough to eliminate or reduce aerosolization upon pouring of the coated enzyme preparation compared to ed enzyme particles. For example, the term “non- aerosolizable” can refer to a coated or encapsulated enzyme preparation where at least about 90% ofthe particles are between about #40 and #140 mesh in size, or between about 106 to 425 um, or where at least about 75% ofthe particles are between about #40 and #80 mesh, or about 180 to 425 um. The term “non aerosolizable” can also refer to a coated or encapsulated enzyme preparation where less than about 35, 30, 25, 20, 15 or % ofthe particles can be sieved through #100 mesh (150 um). In some embodiments, the term “non-aerosolizable” refers to a coated or ulated enzyme preparation where less than about 20% or less than about 15% of the particles can be sieved through #100 mesh (150 um).

As bed and referred to herein, suitable pancreatic/digestive enzymes and suitable coatings can be used in the compositions and s of this invention. The choice of suitable enzymes and of suitable lipid coatings, including choice of the type or amount of enzymes or coating, are guided by the speciﬁc enzyme needs of a subjects, and the selected diseases to be treated. The encapsulated enzyme preparations that are one aspect of this invention have not been previously described.

Some embodiments relate to speciﬁc blends of enzymes and lipids selected for delivery in subjects with ADD, ADHD, autism, and other neurological and behavioral ers susceptible to treatment with digestive/pancreatic enzymes based on the transit times in the human gastrointestinal tract. It can ﬁlrther be based upon the need of a subject to be treated for s components of the digestive enzymes. Further, provided herein are embodiments that relate to improvement ofthe delivery of digestive enzymes to humans based speciﬁcally upon required delivery times, and dissolution proﬁles.

While general methods for g certain sensitive ic substances have been described, see, e. g., US Patent No. 6,251,478, hereby incorporated by reference, the encapsulated bioactive substance of this invention is an enzyme preparation comprising a core containing ive enzymes comprising or consisting of multiple proteases, lipases and amylases, and a coating which comprises or consists essentially of an emulsif1able lipid.

Additives can be blended with the emulsif1able lipid. Selection of the lipid(s) and additives will control the rate of release of the bioactive nce. In the case of the digestive and or pancreatic s, the lipid coat must be uniquely chosen to release the bioactive substance in the area of the ive tract selected for release to ze treatment.

The invention r relates to the administering of the coated and/or encapsulated enzyme preparation in a sachet or pouch preparation for ease of ry to subjects and adults. In some embodiments, the invention speciﬁcally relates to the administration of a coated enzyme particle preparation, housed in a sachet or pouch. This facilitates administration, ing but not limited to, administration in food or drink, direct stration into the oral caVity, or administration directly into the GI system through an NG-tube, G-tube or other GI entrances or deliveries.

In some embodiments, each dose contains about 100 to 1500 mg of coated or encapsulated enzyme preparation, and each dose can contain about 100, 150, 200, 250, 300, 350, 400, 450, 500, 550, 600, 650, 700, 750, 800, 850, 900, 950, 1000, 1050, 1100, 1150, 1200, 1250, 1300, 1350, 1400, 1450, or 1500 mg of coated or encapsulated enzyme preparation. “About” can include 80 to 125% ofthe recited preparation. Each dose can also be plus or minus 10% ofthe recited weight. In one embodiment each does will have a protease actiVity of not less than about 156 USP units/mg :: 10%. The protease ty can also be not less than about 100, 105, 110, 115, 120, 125, 130, 135, 140, 145, 150, 155, 160, 165, 170, 175, 180, 185, 190, 195, or 200 USP units/mg.

In other ments, at least two doses of a composition comprising a therapeutically effective amount of the coated digestive enzyme ations can be administered in the methods described herein. In certain embodiments, about 80% ofthe enzyme is released by about 30 minutes in a dissolution test performed at pH 6.0. In other embodiments, about 80% ofthe enzyme is released by about 30 minutes after the coated digestive enzyme preparations reach the small intestine.

Delivery of enzymes to humans can be improved by reducing the use of excipients, extenders and solvents currently used in the ations for delivery of digestive enzymes to humans. For example, the encapsulated digestive enzyme preparation can contain only one excipient, which increases the safety of administration by decreasing the chance of an allergic response. In one embodiment, the ent is hydrogenated soy oil.

Because, in some embodiments, the lipid encapsulation method does not require the enzyme preparation to be treated with solvents, extenders and excipients to facilitate ﬂow or improve stability, one aspect of the invention includes a ” preparation of GRAS substances (generally regarded as safe) to be administered. The reduction in the use of solvents, extenders excipients and other additives permitted by the methods of this invention reduces the exposure of subjects administered the enzyme replacement, to potential allergens, thereby producing a hypoallergenic enzyme preparation that ﬁlrther enhances its potential uses in the treatment of subjects who might otherwise develop an allergic response to treatment. Administration ofthe coated enzyme ations of this invention can thus reduce exposure to potentially toxic nces and will also reduce the possibility of allergy ion. Accordingly, in some embodiments, the encapsulated digestive enzyme preparation is lergenic.

Digestive s can be safely administered. The lipid coat adds weight to the enzyme preparation, which reduces the potential for lization. Previous uncoated enzymes have been shown to become lized, and can therefore be inhaled and contact the nasal caVity or the lungs, causing injury to the mucosa of those administered and those administering the enzyme preparation.

Sachet preparations can be improved for delivery to subjects. Provided herein are means for administration of a coated digestive enzyme preparation, housed in a sachet which allows for particular types of administration including but not limited to administration in food, drink, or direct administration into the oral caVity or directly into the GI system through a NG-tube, G-tube or other GI ces. The sachet, which represents a unit dosage or multiple doses for a day, represents a single unit dose. The sachet of a trilaminar foil allows the enzyme /lipid powder to remain , and allows for ease of administration.

In another embodiment, the rate of release of the pancreatic/digestive enzyme from an encapsulated enzyme preparation can be controlled upon exposure to a solvent. In some aspects, the method comprises ng an emulsiﬁable lipid with an amount of one or more additives to obtain a lipid blend; and coating the digestive enzyme particle with the blend to form an encapsulated digestive enzyme preparation ning particles comprising a core which ns the enzyme, and a coating which contains the lipid. In some embodiments, the emulsif1able lipid is a blend where the emulsif1able lipid and additive are not the same, and where the rate of release of the enzyme from the encapsulated composite upon exposure to a solvent is decreased as the amount of additive is increased. In the alternative, the rate of release of the enzyme from the encapsulated composite upon exposure to a solvent is sed as the amount of ve is decreased.

The lipid coating surprisingly does not appear to be reduced or destroyed by HCl (hydrochloric acid) present in the stomach, thereby protecting the enzyme from degradation following administration until the enzyme preparation s its target region in the GI tract. Further the lipid coat reduces the exposure of the enzyme to attack by water, thereby ng hydrolysis, and r protecting the digestive enzymes from degradation. In one embodiment an excipient containing only lipid can be used to coat or encapsulate digestive enzyme particles containing lipase.

] The use of digestive enzymes for the treatment of c disease targets can be made possible by preparing encapsulated digestive enzyme composite having ing release characteristics. Since various neurological and behavioral diseases can impact the gastrointestinal systems in humans in various ways, the use of speciﬁc enzyme preparations and the ensuing encapsulation can make the difference as to where and for what duration oftime the enzyme preparation is delivered.

In cases of administration to subjects where delivery of lipases is required for effective treatment, the dissolution profile of the enterically—coated digestive enzymes needs to favor a longer delay in the release of the enzymes, as well as the delivery of a high lipase formulation.

In one embodiment ent of subjects with autism who require delivery ease enzymes for effective treatment, the lipid encapsulate can be modified to deliver the protease during an r transit time window, in the proximal small intestine, to optimize protein digestion. In another example, for subjects who have slow GI transit times due to the dysautonomic nature of their neurological condition, still another release e is required to deliver enzymes for effective treatment. The lipid and/or ve selection will be made to obtain enzyme release at later times aﬁer administration.

Transit times for digestive enzymes through the digestive system can be controlled by layering lipids, or through encapsulation with specific lipid types. In certain aspects, provided herein is the use of a composition containing a ed blend of enzymes and lipids for delivery in ts susceptible to treatment with pancreatic/digestive enzymes, based upon the transit times in the gastrointestinal s of humans. 2013/020183 The improved ﬂow qualities can facilitate packaging of the coated digestive enzyme preparations into, for example, pouches or s.

] In one aspect, lipid encapsulation can be used to make a coated digestive enzyme preparation for speciﬁc delivery times within the human gastrointestinal (GI) tract ed for use in the treatment of a speciﬁc disease or condition. This disease or condition can be caused by or characterized by a digestive deﬁcit that can be treated by the administration of ive enzymes to the appropriate region of the GI tract. The ogical or behavioral disease or condition is one not traditionally associated with the digestive system, where one or more ms can be treated by administering an effective amount of a pancreatic and/or digestive enzyme preparation.

Thus, provided herein is a lipid encapsulation of speciﬁc enzymes targeted for use in the treatment of speciﬁc diseases, and the encapsulation method includes the amount and type of lipids used in the methods of described herein for the preparation of the encapsulated digestive enzyme composite. The present embodiments also relate to s ofmaking the enzyme preparations by lipid coating and/or encapsulation of pancreatic and/or digestive enzymes. The methods comprise providing an emulsiﬁable lipid, and coating pancreatic/digestive enzyme particles with the lipid, where the pancreatic/digestive enzymes comprise 5-90% ofthe coated enzyme preparations by weight. In some aspects the uncoated pancreatic/digestive enzyme particles have a size range of about 105-425 um.

In one ment, a method is described herein for ing an ulated digestive enzyme preparation, the method comprising a) screening uncoated digestive enzyme particles to obtain particles of a suitable size for encapsulation; and b) coating the screened digestive enzyme particles with an emulsiﬁable lipid to form coated or encapsulated digestive enzymes containing a core which contains the pancreatic/digestive enzyme and a coating which contains the emulsiﬁable lipid. In some embodiments, the encapsulated digestive enzyme preparation is a controlled release digestive enzyme preparation, which can have enhanced ﬂow properties.

Screening ofthe particles can include quality control steps to improve the activity, appearance or particle size of the digestive . For e, the particles can be ed to determine enzyme ty content, and/or visualized using chromatographic, microscopic or other analytical methods. The particles can also be screened to obtain particles of a suitable size for encapsulation by removing les that are too ﬁne or too large. For example, the particles can be sieved to obtain particles of a suitable size or more uniform size range for encapsulation. As a ﬁarther example, the particles can be sieved through USSS #40 mesh and through USSS #140 mesh. Particles that pass h the #40 mesh but are retained by the #140 mesh are of an appropriate size range for coating or encapsulation Particles can also be screened by sieving through USSS #140, #120, #100, #80, #70, #60, #50, #45, or #40 mesh, or any combination thereof.

Enzyme preparations supplied by the API supplier can be provided as irregular shaped, and multi-sized particles, with uneven edges, and much clumping, and containing some crystalline salt les (data not . Uneven particle size and shape reduces ﬂow properties, and interferes with packaging. In addition, pouring uncoated enzyme into the mouth of a subject would be difﬁcult, and potentially can cause too much or too little of the enzyme to be red. In one embodiment processing the digestive enzyme particles according to methods described herein yields a non-dusty, free-ﬂowing particulate preparation suitable for sachet packaging and for pouring onto food or drink. In addition, as discussed throughout, the use of lipid encapsulation to prevent aerosolization, and therefore increase safety, to increase ﬂow properties which enhance cturing of a pharmaceutical is an embodiment disclosed .

The size distribution of particles in an ary raw enzyme preparation may be determined (data not . Large particles (>40 mesh) and very small particles (<140 mesh) are generally not suitable for proper encapsulation and can be removed by screening. In order to increase the ﬂow properties of the encapsulated pancreatic enzyme preparation, ive enzyme particles can be sieved to remove ﬁnes and overly large particles, for e by including only particles of sizes 40-140 mesh, or about 105 to 425 microns. In some embodiments, the coated ive enzyme preparation containing 80% digestive enzyme by weight is made by coating sieved pancreatic enzyme particles with a hydrogenated vegetable oil using 20 lbs. of enzyme particles and 5 lbs of hydrogenated vegetable oil.

In some embodiments, the temperature ofthe lipid or lipid blend is maintained between 100° F and 120° F before application to the digestive s, which are not heated.

In some embodiments, the lipid should be present in the preparation at a minimum amount of about 5% by weight ofthe ulated composite, preferably about %, and more preferably about 50% by weight ofthe encapsulated ite. The maximum amount ofpancreatic/digestive enzyme present in the encapsulated composite WO 03746 is about 95% by weight ofthe composite, preferably about 90%, and more preferably about 85% ofthe encapsulated composite. The emulsif1able lipid can be any lipid or lipid-derived material that emulsif1es or creates an emulsion yet has a melting point which allows the emulsiﬁable lipid to be a solid at typical storage temperatures, for example, 23° C.

“Emulsifiable lipids” as used herein means those lipids which contain at least one hydrophilic group and at least one hydrophobic group, and have a structure capable of forming a hydrophilic and hydrophobic interface. These chemical and/or physical properties, mentioned above, of an emulsif1able lipid permit emulsif1cation.

Examples of interfaces include, for example, micelles and bilayers. The hydrophilic group can be a polar group and can be charged or uncharged.

The emulsif1able lipid can be d from animal or vegetable origins, such as, for e, palm kernel oil, soybean oil, cottonseed oil, canola oil, and poultry fat, ing hydrogenated type I vegetable oils. In some embodiments, the lipid is hydrogenated. The lipid can also be saturated or partially saturated. Examples of emulsif1able lipids include, but are not limited to, monoglycerides, diglycerides, fatty acids, esters of fatty acids, phospholipids, salts thereof, and combinations thereof The emulsif1able lipid is ably a food grade emulsif1able lipid. Some examples of food grade emulsif1able lipids include sorbitan monostearates, sorbitan tristearates, calcium yl lactylates, and m stearoyl lactylates. Examples of food grade fatty acid esters which are emulsif1able lipids e acetic acid esters of mono- and diglycerides, citric acid esters of mono- and di-glycerides, lactic acid esters of mono- and di-gylcerides, polyglycerol esters of fatty acids, ene glycol esters of fatty acids, and diacetyl tartaric acid esters of mono- and diglycerides. Lipids can include, for example, enated soy oil.

Any emulsiﬁable lipid can be used in the methods and products sed herein. In certain embodiments the emulsif1able lipid used will produce non- agglomerating, non-aerosolizing enzyme ation particles.

In other embodiments, the method relates to preparation of an encapsulated, controlled release digestive enzyme ation with enhanced ﬂow properties, the method comprising: a) blending an emulsif1able lipid with one or more additives to obtain a blend; and b) coating screened digestive enzyme with the blend to form an encapsulated digestive enzyme containing a core which contains the ive enzyme and a coating which contains the blend of emulsif1able lipid.

The coating ofthe enzyme with the lipid allows for the enzyme to become more uniform in size and shape, but reduces the jagged edges associated with the raw enzyme, and allows for ease of administration and ease of manufacturing, as the ﬂow properties associated with the covered enzyme will allow for the manufacturing machinery to easily fill the sachet/pouch with the enzyme and reduces overﬁlling or under ﬁling ofthe sachet. The unit dose packaging reduces the ability of the child to open the multi dose can/box/ or other container. The trilaminar foil pouch or sachet ﬁarther reduces the ability of a t to open the sachet/pouch, and over e the enzyme.

] In r embodiment, provided herein is a method of controlling the rate ofrelease of a digestive enzyme from the encapsulated preparation by using a lipid blend to coat the digestive enzyme. The method es blending an f1able lipid with one or more additives to obtain a blend, and coating the digestive enzyme with the blend to form an encapsulated digestive enzyme containing a core which contains the digestive enzyme and a coating which contains the blend of f1able lipid. The rate of release ofthe enzyme from the encapsulated preparation upon exposure with a solvent is decreased as the amount of additive is increased. In the alternative, the rate of release of the enzyme from the encapsulated composite upon exposure with a t is increased as the amount of additive is decreased. Thus, the nature of the g allows for controlled release of the enzyme from the encapsulate.

Non-emulsiﬁable lipids do not s the chemical and/or physical properties related to emulsif1cation as described above and e any lipid, lipid derived material, waxes, organic esters, or combinations thereof Non-emulsifiable lipids generally do not emulsify by themselves. Non-emulsiﬁable lipids can be used as additives so long as the properties of the coating, and constituent lipids, permit emulsif1cation. Non-emulsifiable lipids, such as, for example, triglycerides, can be blended with an emulsif1able lipid disclosed herein. The non-emulsif1able lipid can be derived from animals, vegetables, mineral, or synthetic origins. The non-emulsifiable lipid is preferably hydrogenated, and can be saturated or partially saturated, and includes, but is not limited to triglycerides. In a preferred embodiment, the coating contains a blend ofmonoglycerides and triglycerides applied to a atic/digestive enzyme.

The inclusion of one or more additives with an emulsiﬁable lipid disclosed herein is used to control emulsif1cation of the coating and release of the . For e, the additive, triglyceride, can be blended with monoglycerides (e.g., an emulsif1able , to control emulsif1cation of the coating and thus control (e.g., decrease) the rate of release of the enzyme from the composite. As a ﬁarther example, one or more additives, such as a eride and a triglyceride can be blended with the emulsif1able lipid to control the rate of release of the enzyme. Hydrogenated vegetable oils can n emulsifying agents, such as soy lecithin or other components.

Properties including mechanical strength, g point, and hydrophobicity can be considered when choosing a le lipid coating for the ive enzyme. Lipids having lower melting points or more polar, hydrophilic properties were generally less suitable for encapsulation because they resulted in product that would cake under accelerated storage stability conditions. Enzyme preparations made using, for example, hydrogenated soy oil, hydrogenated castor wax, and camauba wax all demonstrated good pouring and no caking.

The wax can be paraffin wax; a petroleum wax; a mineral wax such as ozokerite, ceresin, or montan wax; a vegetable wax such as, for e, camuba wax, bayberry wax or ﬂax wax; an animal wax such as, for example, spermaceti; or an insect wax such as beeswax.

Additionally, the wax material can be an ester of a fatty acid having 12 to 31 carbon atoms and a fatty alcohol having 12 to 31 carbon atoms, the ester having from a carbon atom content of from 24 to 62, or a mixture thereof Examples include myricyl ate, cetyl palmitate, myricyl cerotate, cetyl myristate, ceryl palmitate, ceryl certate, l melissate, stearyl palmitate, stearyl myristate, and lauryl e.

In a ﬁarther embodiment, a method is disclosed herein for controlling rate ofrelease of a pancreatic/digestive enzyme from an encapsulated composite upon re to a solvent. The method includes coating the enzyme with an amount of an emulsif1able lipid to form an ulated pancreatic enzyme substance composite, wherein the rate of release of the enzyme from the encapsulated composite is decreased as the amount of emulsif1able lipid based on total weight of the encapsulated composite is increased. In the alternative, the rate of e of the pancreatic enzyme from the encapsulated composite is increased as the amount of emulsiﬁable lipid based on total weight ofthe ulated composite is decreased. The emulsif1able lipid useﬁal in this embodiment can consists essentially of one or more monoglycerides.

The solvent in which a lipid emulsif1es can be an aqueous solvent. The aqueous solvent interacts with the hydrophilic groups present in the emulsif1able lipid and disrupts the continuity of the coating, resulting in an emulsion between the aqueous solvent and the lipids in the coating, thus releasing the bioactive substance from the composites.

Provided below are s ofusing encapsulated pancreatic or digestive enzyme cores for treatment ological ions or disorders to achieve speciﬁc ends. Provided herein are s for lipid encapsulation of medications for human consumption which have the characteristics of a time-released medication, and which utilize the lipid encapsulation for ity. Described below are methods for the preparation of an encapsulated enzyme preparation comprising a coating of emulsiﬁable lipid and a digestive enzyme suitable for the time-speciﬁc arid/or site-speciﬁc targeted release along the GI tract.

Aspects and embodiments ofthe instant embodiments stem from the surprising and unexpected discovery that certain pharmaceutical dosage preparations comprising a coating of emulsiﬁable lipid and a digestive enzyme can have novel potentiated activity and unexpected favorable release and dissolution proﬁles and tion kinetic parameters along the various portion of the GI tract. These characteristics are useful for ating a speciﬁc bioactive enzyme for site speciﬁc targeted release along the GI tract.

In some cases, determination ofwhether a subject is in need oftreatment with an effective amount of digestive enzymes can be based on a determination that a t has an enzyme deﬁciency. In other cases, determination ofwhether a subject is in need tment with an effective amount of ive enzymes can be based on a determination that a subject has an abnormal chymotrypsin level as measured in the GI tract, directly or at the end of the GI tract as a measure of fecal chymotrypsin. In yet other cases, determination ofwhether a subject is in need oftreatment with an effective amount of digestive enzymes can be based on a determination that a t has an abnormal stool pH level. In yet other cases ination her a subject is in need oftreatment with an effective amount of digestive enzymes can be based on a determination that a subject has abnormal PCT and stool pH levels.

Levels of amino acids which are the breakdown products ofprotease digestion can be measured as well to determine if there is a need for enzyme replacement.

Low and absent proteases will leave a dearth of amino acids, and amino acid pool in the body will be altered and subsequent determination of the need for s to break down proteins can be determined by the measurement of amino acids in the blood.

As enzyme replacement may be necessary as a result of enzymes such a the proteases either being secreted in insufﬁcient amount, in normal amounts which are then degraded through an unsuitable environment in the small intestine, or if the enzyme for example the proteases are secreted in a defective or inactive form will all necessitate the need for exogenous enzyme replacement.

Further stool pH will be low or abnormally low in the e of protein breakdown, and may signify the need for proteases replacement. Therefore an abnormal blood or stool pH may indicate the need for enzyme replacement.

Further in the examination of nutrient uptake and nutrient digestion may also signal the need for enzyme ement and/or an abnormal vitamin intake such as vitamin K could be potentially indicative of autism or the formation of autistic motology, or other co-morbid condition.

] In one aspect a method disclosed herein comprises using the enzyme formulations disclosed herein to treat subjects and other subjects with autism who also have an enzyme ncy. The enzyme ncy could be determined by any method used in determining or diagnosing an enzyme deﬁciency. In one aspect the determination or diagnosis can be made by ting symptoms, including eating , self-imposed dietary restrictions, and symptoms of eating disorders and/or gastrointestinal ers.

In other aspects, the determination can be made on the basis of a biochemical test to detect, for example, levels or activities of s secreted, excreted or t in the GI tract, and/or by determining the presence of a mutation in a gene or aberrant expression of a gene encoding one or more digestive enzymes. The enzyme deﬁciency can also be determined, for example, by detecting a mutation or aberrant expression of a gene encoding a product ting or otherwise affecting expression or activity of one or more digestive s.

In another aspect, the determination ofbehavioral symptoms and symptom improvement can be ed by the administration of enzymes and especially proteases to improve an aspect of the behavior. The behaviors include but are not limited to: irritability, agitation, aggression, ; lethargy, social withdrawal; social isolation, stereotypic behavior ing neuro stimming (autistic stereopathy) and obsessive compulsive behaviors hyperactivity, noncompliance; inappropriate speech. Further the behaviors can encompass, a lack of expressive or receptive language, limited vocabulary, lack or low levels of executive ﬁanction, as well as restricted and repetitive movements and other oceptive issues which manifest in autism as well as other neurological conditions.

In some aspects, a subject to be treated can either have symptoms of autism or other co-morbid neurological or behavioral manifestations or have a genetic based co-morbidity. Further the assessment of the need for enzyme replacement could also ine the need for treatment with the enzyme delivery systems described herein.

In certain aspects, ts who are determined to have autism based on clinical symptoms but not a co-morbidity such as a genetic co-morbidity, are treated with the enzyme delivery systems described herein. However, subjects who are determined to have autism based on clinical symptoms and a co-morbidity, who nevertheless also test abnormally low for FCT level or ve using another tor of GI pathogens and/or low digestive enzyme activity or expression can also be treated with the enzyme delivery systems disclosed herein.

The need for enzyme replacement based upon symptomology has utility as the degradation of certain enzymes makes testing difficult. A direct marker such as the measurement of fecal chymotrypsin, as well as a secondary or surrogate marker such as that seen with low circulating amino acids could be utilized for example to determine the need for the enzyme preparations described herein.

In one aspect, the ination of an enzyme deﬁciency can be made using a test for fecal rypsin levels. s such as PCR or other amplification, SNP ion, sequencing, and/or DNA combing can be used to detect the presence of a mutation or presence of short RNA sequences which interfere with expression of one or more genes encoding a digestive enzyme. For example, the mutation can in a gene ng a digestive enzyme which decreases or eliminates the activity of the enzyme.

As r example, the mutation can be mutation in the MET gene, a gene encoding the pleiotropic MET receptor tyrosine kinase See Campbell et al., PNAS 103(46), 16834-39 (2006). These mutations can include, for example, the MET promoter variant rs1858830 C allele, and or mutations in the MET signaling pathway such as a haplotype of the SERPINEl gene, or the rs344781 PLAUR promoter variant T allele.

] The enzyme formulations disclosed herein are suited for use in delivering digestive enzymes to subjects with autism, autism um disorders, ADD, ADHD, and other neurological diseases or conditions in need of enzyme treatment. The co-morbid ms of other neurological or behavioral ions may also be amenable to treatment with the said enzyme preparation described herein.

Fallon has described certain methods and enzyme compositions for use in ng subjects and other subjects, with autism, for example, US. Patent Nos. 7,138,123, 831, 6,632,429, 6,534,063, hereby incorporated by reference as if set forth in ﬁlll .

] In the experiments described herein, several factors were discovered that d for the unexpected enhanced / potentiated efficacy and property. For example, it was discovered that certain encapsulation enzymatic preparations comprising soy oil exhibited certain surprising characteristics that led to improvements in the site-specific activity, release/dissolution proﬁle, and ease of manufacturing, packaging and storage.

Without being bound to a ular theory of operation, the skilled artisans will appreciate that other methods of sample preparation and/or formulation that can also yield these advantageous parameters are also contemplated herein.

The encapsulation of an enzyme as described herein did not by deﬁnition anticipate the properties exhibited by the ion. For example, the stability of the t over 36 months under standard and nonstandard conditions was not obviated by the known ality ofthe encapsulation process. The properties of the enzyme as formulated by ratio described herein could not have anticipated the protective qualities of the combined enzyme-encapsulation material x.

The concentration of digestive enzymes in the pharmaceutical composition will depend on the degradation, inactivation and excretion rates of the enzymes, the physicochemical characteristics of the enzymes, the dosage schedule, the dosage form, and amount administered as well as other factors known to those of skill in the art.

The pharmaceutical composition can be administered at once, or can be divided into a number of smaller doses to be administered at intervals of time. It is understood that the precise dosage and duration of treatment is a ﬁanction of the wound and can be determined empirically using known testing protocols or by extrapolation from in vivo or in vitro test data. It is to be ﬁarther understood that for any particular subject, specific dosage regimens should be adjusted over time according to a t need and the professional judgment ofthe person administering or supervising the administration of the compositions, and that the tration ranges set forth herein are exemplary only and are not intended to limit the scope or practice of the d compositions. In some embodiments, the compositions are provided in unit dosage forms suitable for single stration, or multi-dose administration, of a precise dose. 2013/020183 Dosing should be given with food to aid in the absorption of the nutrients and to facilitate breakdown. The invention anticipates release of the enzyme over time, and this can be expanded to a time release formulation whereby once a day or other long acting affects can come from the administration of the enzyme.

The compositions can be stered either alone or more typically in combination with a conventional pharmaceutical carrier, ent or the like. The term “excipient” is used herein to be any ient other than the compound(s) (enzymes) used in the composition as described herein and known in the art. Lipid encapsulation is one preferred embodiment, but other carriers and excipients can be utilized to deliver the enzyme ation.

Methods ofpreparing such dosage forms are known, or will be apparent, to those skilled in this art; for example, see Remington: The Science and Practice of Pharmacy, 21st Edition (Lippincott ms & Wilkins. 2005).

Appropriate dosages will depend on a subject (species, age, weight, health, etc), the severity of the condition, the type of formulation and other factors known to those having ordinary skill in the art. It is to be noted that concentrations and dosage values can vary with the severity of the ion, weight of a subject, the amount and types of food eaten and other factors as determined by the administering practitioner. It is to be ﬁarther understood that for any particular subject, speciﬁc dosage ns should be adjusted over time according to a subject need and the professional judgment of the person stering or supervising the administration of the compositions.

In one embodiment a composition can be administered 1 or more times a day, such as l, 2, 3, 4, 5, 6, 7, 8, 9, or 10 times a day preferably with food. Speciﬁc dosage forms or time release applications can be administered without food. In another embodiment, a composition can be administered orally 3 times a day with or t food, or with each substantial meal. The composition can be in tablet, capsule, granular, in sprinkle form, and have taste maskers present for ease of ry to subjects. The compositions can be packaged in a unit dose e with the drug remaining stable for over 30 months.

Experiment I examined the changes seen in subjects administered Formulation 1 described herein when compared to subjects who received a placebo.

Formulation l is a granulated pancreatin soy lipid-encapsulated drug product that has a protease activity of not less than 156 USP units/mg. A single dose of Formulation l is provided in a pouch or sachet at about 900mg. Subjects aged 3-8 diagnosed with autism were administered a composition of formula 1 or a placebo. While females are typically known to have more severe cases of autism, one surprising discovery made by the present inventors is that girls were found to improve more than boys aﬁer treatment with compositions described herein. Boys were also identiﬁed as exhibiting improvement in one or more symptoms of autism. Furthermore, ts with more severe cases of autism as a whole had greater improvements as ed to subjects with less severe cases of autism when treated with itions bed herein. Provided herein is a method oftreating an autistic child, comprising administering to a subject in need thereof a composition described herein. In one embodiment, a subject to be treated with such methods is autistic. In another embodiment, a subject to be treated is female. In yet r embodiment, a subject to be treated is male. A subject can be administered a single dose or multiple doses of the compositions. In another embodiment, a subject treated with such s exhibits an improvement in autism of at least about 5%, about %, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% ed to a subject treated with a placebo.

The factors (subscales) of the Aberrant Behavior Checklist (ABC) scale are as follows: (I) irritability, ion, crying; (II) lethargy, social withdrawal; (III) stereotypic behavior; (IV) hyperactivity, noncompliance; and (V) inappropriate speech.

At a terminal FCT level of 6.0 Units/gram (fresh) or 9.0 (frozen) or r of feces, additional improvements ed following treatment with compositions described herein include body weight, ABC stereotypical behavior, ABC hyperactivity, ABC irritability, ABC lethargy/ social withdrawal.

At a terminal FCT level of 6.0 Units/gram (fresh) or 9.0 (frozen) or greater of feces, along with an FCT 3.5 or greater from baseline, the t ors determined that there was statistically icant improvement in all 4 ABC scales — irritability, hyperactivity, lethargy/ social withdrawal, and stereotypical behavior.

The present inventors have found that subjects treated with compositions described herein trated overall better improvement as compared to treatment with aripiprazole (Abilify®) on the ABC irritability scale. In general, females who experience an increase in FCT have an improvement is seen in four ABC scales: ABC stereotypical behavior, ABC hyperactivity, ABC irritability, ABC lethargy/ social withdrawal.

Provided herein is a method of ing all four subscales of the ABC scale in a subject, comprising administering to a subject in need thereof a composition described herein. In one embodiment, a subject to be treated with such methods is autistic. In another embodiment, a subject to be treated is female. In yet another embodiment, a subject to be treated is male. In another embodiment, a t treated with such methods exhibits an improvement in all four subscales of the ABC scale of at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a subject treated with a placebo.

In one embodiment, subjects treated with a composition described herein exhibit an improvement in irritability and/or agitation ing to the ABC scale.

Provided herein is a method of treating irritability and/or agitation in a subject, comprising administering to a subject in need thereof a composition described herein. A subject can be administered a single dose or le doses of the compositions. In another embodiment, a subject treated with such methods exhibits an improvement in irritability and/or agitation of at least about 5%, about 10%, about 15%, about 20%, about %, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a subject treated with a placebo.

In another embodiment, subjects treated with a composition described herein exhibit a signiﬁcant improvement in social withdrawal and/or lethargy based on the ABC scale. Provided herein is a method of improving social withdrawal and/or lethargy in a subject, comprising administering to a subject in need thereof a composition described herein. A subject can be administered a single dose or multiple doses of the compositions. In another ment, a subject treated with such methods exhibits an improvement in awal and/or lethargy of at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a subject d with a o.

In one embodiment, subjects treated with a composition described herein exhibit a significant improvement in hyperactivity based on the ABC scale. Provided herein is a method of decreasing hyperactivity in a subject, comprising administering to a t in need f a composition described herein. A subject can be administered a single dose or le doses of the itions. In r embodiment, a subject treated with such methods ts an ement (1.6. a decrease) in hyperactivity of at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a subject treated with a placebo.

Provided herein is a method of improving stereotypic behavior in a subject, comprising administering to a subject in need thereof a composition described herein. In one embodiment, a t to be treated with such methods is autistic. A subject can be administered a single dose or multiple doses of the compositions. In another embodiment, a subject treated with such s exhibits an improvement in stereotypic behavior of at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a subject d with a placebo.

The present inventors identiﬁed that all of the oral measurements that improved aﬁer treatment with the present s, did so in correlation with improved FCT 1eve1s.

Provided herein is a method of improving one or more behaviors in a subject, comprising stering to a t in need thereof a composition described herein. In one embodiment, a subject to be treated with such methods is autistic. A subject can be administered a single dose or multiple doses of the compositions. In another embodiment, a subject treated with such methods exhibits an improvement in one or more behaviors of at least about 5%, about 10%, about 15%, about 20%, about 25%, about %, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a subject treated with a placebo.

Provided herein is a method of improving inappropriate speech in a subject, sing administering to a subject in need f a composition described herein. A subject can be administered a single dose or multiple doses of the compositions.

In another ment, a subject d with such methods exhibits an improvement (i.e., decrease) in inappropriate speech of at least about 5%, about 10%, about 15%, about %, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a subject treated with a placebo.

In yet another embodiment, subjects treated with a composition described herein exhibit an improvement in the overall 5 subscales, which include the three described above, as well as typy and inappropriate speech. ed herein is a method of improving one, two, three, four, or ﬁve of the les of the ABC scale in a subject, comprising administering to a subject in need thereof a composition described herein. A subject can be administered a single dose or multiple doses of the itions. In another embodiment, a subject d with such methods exhibits an improvement of at least about 5%, about 10%, about 15%, about %, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% of one, two, three, four, or ﬁve subscales of the ABC scale compared to a subject treated with a placebo.

In one embodiment the lethargy and hyperactivity scales were both reduced whereas, typically, they are reciprocal scales — z'.e., an ement in lethargy also results in an increase in hyperactivity and vice versa.

Provided herein is a method of improving lethargy and hyperactivity in a subject, comprising administering to a subject in need thereof a composition described herein. A subject can be administered a single dose or multiple doses of the compositions.

In another embodiment, a subject treated with such methods exhibits an ement in lethargy and hyperactivity of at least about 5%, about 10%, about 15%, about 20%, about %, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a subject treated with a o.

The present methods are efﬁcacious in subjects that hold mild and or moderate levels of lethargy, ctivity, social withdrawal, and bility.

The present methods are even more efﬁcacious in subjects with increased levels of lethargy, hyperactivity, social withdrawal, and bility.

The compositions described herein, in certain embodiments, behave like a partial dopamine agonist.

In one embodiment the compositions described herein accomplish this effect without a ng effect or an increase in neurological symptoms (such as dizziness, Parkinsonisms, dystonia, akathisia, somnolence, fatigue, extrapyramidal disorders, tremor, and drooling), as compared to other approved drugs for autism. In one embodiment, treatment of a subject with such s does not cause a sedating effect.

In another embodiment, treatment of a subject with such methods does not cause an increase in one or more neurological symptoms, wherein the neurological ms are ess, Parkinsonisms, dystonia, sia, somnolence, fatigue, extrapyramidal disorders, tremor, and drooling.

In one embodiment, improvement in one or more symptoms in subjects aﬁer treatment with a ition described herein is accomplished without weight gain.

] Furthermore, these positive changes in the subscales can be accomplished/met t any side effects in accordance with FDA ing rds (a rate greater than 5%).

Provided herein is a method of treating a subject exhibiting one or more of the ABC subscales: (I) irritability, agitation, crying; (II) lethargy, social withdrawal; (III) stereotypic behavior; (IV) ctivity, noncompliance; and (V) inappropriate speech, comprising administering to a subject in need thereof a composition described , wherein the side effects of treatment are without any side effects in accordance with FDA reporting standards (a rate greater than 5%).

In some embodiments, changes that occur in the subscales occur at week 4 and continue to improve thereaﬁer. Within subjects of ages 3 to 8, there is no age effect, that is, the compositions are equally efficacious amongst all age groups. No geographical correlation was observed in ts treated with compositions described herein.

Improvements were observed in both receptive and expressive language as measured by the Expressive lary Test (EVT) and the Peabody Picture Vocabulary Test.

The Expressive Vocabulary Test (EVT) is a subjectively administered, norm-referenced test of expressive vocabulary and word retrieval. For 38 labeling items, the er points to a picture or a part of the body and asks a question. On 152 synonym items, the examiner presents a picture and stimulus word(s) within a carrier phrase. The examinee responds to each item with a one-word answer. All stimulus pictures are in ﬁlll color, carefully balanced for gender and ethnic representation. Results are assessed based on Age- and Grade-Based rd Scores, Percentiles, Normal Curve Equivalents (NCEs), Stanines, Age and Grade lents, Growth Scale Value (GSV).

The Peabody Picture Vocabulary Test measures a subject's receptive (hearing) vocabulary for Standard American English and provides a quick estimate of their verbal ability or scholastic aptitude. An examiner presents a series of pictures to each person. There are four pictures to a page, and each is ed. The examiner states a word describing one ofthe pictures and asks a subject to point to or say the number of the picture that the word describes. Item responses can also be made by multiple choice selection depending upon subject's age. The total score can be converted to a percentile rank, mental age, or a standard deviation IQ score.

Provided herein is a method of ing receptive and expressive language in a subject, comprising administering to a subject in need thereof a composition described herein. A subject can be administered a single dose or multiple doses of the compositions. In one embodiment, a subject treated with such methods exhibits an improvement in receptive and expressive language of at least about 5%, about 10%, about %, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a t treated with a placebo.

Subjects with autism that had aphasia and other potential unknown causes that present as a lack of expressive language manifest speech improvements surprisingly with age appropriate grammatical structure and lary without a learning curve.

Provided herein is a method of improving grammatical structure and vocabulary, comprising administering to a subject in need thereof a composition described herein. A t can be administered a single dose or le doses of the compositions. In one embodiment, a subject treated with such methods exhibits an improvement in grammatical structure and lary of at least about 5%, about 10%, about 15%, about %, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a subject treated with a placebo.

Provided herein is a method of improving l growth scales as well as sed question ceiling levels and reduction in error rates in a subject, comprising administering to a t in need thereof a composition described herein. A subject can be administered a single dose or multiple doses of the compositions. In one embodiment, a subject treated with such methods exhibits an improvement in overall growth scales of at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% ed to a t treated with a placebo. In another embodiment, a subject treated with such methods exhibits an increased question ceiling level and reduction in error rate of at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% ed to a subject treated with a placebo.

Changes in hyperactivity were also observed in the Conners’ 3-teacher report (3-TR) which is the Gold Standard for diagnosing as well as adjusting established medications for Attention Deﬁcit and ion Deﬁcit Hyperactivity Disorders.

Connors’ 3-TR can be administered according to tional methods and scored according the T-score guidelines. Attributes that are assessed include: ss or overactive behavior; excitability and impulsiveness; failing to ﬁnish tasks; inattentiveness and ease of distraction; temper sts; ﬁdgeting; disturbances of other subjects; demands to be met immediately and ease of ﬁustration; ease and frequency of crying; and rapid and drastic mood changes. Each attribute is scored on a scale of 0-3 where 0 = never, seldom; 1 = occasionally; 2 = often, quite a bit; and 3 = very often; very frequent.

Administration ofthe compositions described herein resulted in a signiﬁcant reduction in hyperactivity and improvement in the Global Index of the Conners’ Test.

Provided herein is a method of treating a t, comprising administering to a subject in need thereof a composition described herein, wherein treatment s hyperactivity results in an ement in inattention, learning problems, executive ﬁanctioning, aggression, and peer relations. A subject can be administered a single dose or le doses of the compositions. In one ment, a t treated with such methods exhibits an improvement in inattention, ng problems, executive ﬁlnctioning, aggression, and peer ons of at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a subject treated with a placebo.

Persuasive development disorders can be classiﬁed under the DSM-IV-TR classiﬁcation as an autistic disorder, Asperger’s Disorder, PDD-NOS (including atypical autism), Rett’s Disorder and Childhood Disintegrative er. In another embodiment, treatment improves one or more ofthe attributes of the Conners’ DSM-IV Scale according to conventional scoring. The Conners’ ADHD/DSM-IV Scales (CADS) consist of the items of the CRS-R that best differentiate subjects with ion- Deﬁcit/Hyperactivity Disorder from nonclinical subjects. The DSM-IVTM Symptom Scales ly correspond to DSM-IV criteria for ADHD diagnosis with parent (CAD-P), teacher T) and self-report (CADS-A) forms. Separate measurements for ADHD inattention, ctivity impulsivity, conduct disorder, oppositional deﬁant, and the global impression scale have been made aﬁer treatment with compositions described herein with the same results demonstrating improvement observed. In one embodiment, a subject treated with such methods exhibits an improvement in one or more of the attributes of the Conners’ DSM-IV Scale according to conventional scoring of at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a subject treated with a o.

The compositions provided herein reduce the occurrence of diarrhea in at least the population of ic subjects and most likely for subjects overall for certain types of intestinal disturbances. Provided herein is a method for reducing the occurrence of ea in subjects, comprising administering to a subject in need thereof a composition described . In one embodiment, the child is autistic. In another embodiment, the child is not autistic. In yet r embodiment, administration ofthe present compositions reduces the occurrence of diarrhea by at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% ed to a subject treated with a placebo.

The majority of subjects with autism universally suffers from a n mal-absorption syndrome, and thus undernourished. The present inventors have identified that a pretreatment FCT level of 15.5 mean (frozen) across the entire study population indicated that subjects are universally suffering from a protein sorption syndrome and, thus, are under-nourished. This includes all subjects that are above the 12.6 units/gram (frozen) of chymotrypsin cutoff for the study.

The compositions described herein also were observed to improve diet and weight in subjects. As subjects approached reasonably normal levels of chymotrypsin, the stronger the increases in balanced food consumption, protein intake, vegetable intake, meat intake, cholesterol, vitamin K, m, improvements in glycemic load, and improvements in ABC irritability, social withdrawal/ lethargy and hyperactivity.

] Provided herein is a method of normalizing chymotrypsin levels in a subject, comprising administering to a subject in need thereof a composition described herein. In one embodiment, such treatment increases balanced food consumption, n intake, vegetable intake, meat intake, cholesterol, vitamin K, calcium, improvements in glycemic load. In another embodiment, such treatment es ABC irritability, social awal/ lethargy and ctivity.

At a terminal FCT level of 6.0 Units/gram (fresh) or 9.0 (frozen) of feces or r, the present inventors identified that numerous minerals and vitamins improve following treatment: Plant Based Vitamin A, Carotenoids (alpha and beta ne), Vitamin K, Vitamin E, Vitamin C, Selenium, copper, food folate, lutein, lycopene, magnesium, moisture content of foods, potassium, phosphorus, sodium, polyunsaturated fatty acids, monounsaturated fatty acids, saturated fats, cholesterol, vitamin E, Vitamin K, along with a beneficial decrease in Theobromine. Calcium and Iron (both a positive 2 charge ions), and animal sources ofVitamin A, were not ed to improve.

In general, subjects treated with a composition described herein and which subjects had a level of 40 milligrams or greater of daily copper daily intake and at the same time an FCT level of 6.0 Units/gram ) or 9.0 (frozen) or greater of feces were observed to have an improvement in four ABC scales: ABC stereotypical behavior, ABC hyperactivity, ABC irritability, ABC lethargy/ social withdrawal.

In general, subjects treated with a composition described herein and which had a level of 2000 micrograms or greater daily intake of lycopene, daily intake and at the same time a lutein daily intake level of 500 micrograms or greater improvement is seen in four ABC : ABC stereotypical behavior, ABC hyperactivity, ABC irritability, ABC lethargy / social withdrawal.

] In general, subjects treated with a composition described herein and which had a level of 40 micrograms or greater daily intake of selenium have daily intake improvement in four ABC scales: ABC stereotypical behavior, ABC hyperactivity, ABC irritability, ABC lethargy/ social awal.

In general, with an se in alpha and simultaneously beta carotene improvement is seen in four ABC scales: ABC stereotypical behavior, ABC hyperactivity, ABC irritability, ABC lethargy/ social withdrawal aﬁer treatment with a composition herein (data not shown).

The ic index (G1) is a measure ofthe effects of carbohydrates on blood sugar levels. Carbohydrates that break down quickly during digestion and release glucose y into the bloodstream have a high GI; carbohydrates that break down more slowly, releasing glucose more gradually into the bloodstream, have a low GI. A lower glycemic index suggests slower rates of ion and tion of the foods' carbohydrates and may also indicate greater extraction ﬁom the liver and ery of the products of carbohydrate digestion. A lower glycemic response may equate to a lower insulin demand in some cases, and may improve long-term blood glucose control and blood lipids. The insulin index is also useful for providing a direct measure of the insulin response to a food.

The glycemic index of a food is deﬁned as the area under the two-hour blood glucose response curve (AUC) following the ingestion of a ﬁxed portion of carbohydrate (usually 50 g). The AUC ofthe test food is divided by the AUC ofthe standard (either glucose or white bread, giving two different deﬁnitions) and multiplied by 100. The average GI value is calculated from data collected in 10 human subjects.

Both the standard and test food must contain an equal amount of available carbohydrate.

The result gives a relative ranking for each tested food.

Conventional methods use glucose as the reference food, giving it a glycemic index value of 100 by deﬁnition. This has the advantages ofbeing universal and ing maximum GI values of approximately 100. White bread can also be used as a nce food, giving a ent set of GI values (ifwhite bread = 100, then glucose z 140).

GI values can be reted intuitively as percentages on an absolute scale and are ly interpreted as follows: Classiﬁcation GI range Examples most ﬁuits and vegetables, legumes/pulses, whole Low GI 55 or less grains, nuts, ﬁuctose whole wheat products, i rice, sweet potato, Medium GI 56—69 sucrose, baked potatoes 70 and white bread, most white rices, corn ﬂakes, extruded High GI_ above breakfast cereals, glucose, maltose The present inventors have identiﬁed that, in general, in subjects treated with a composition herein and having a glycemic index of less than 55 and an FCT level of 6.0 Units/gram (fresh) or 9.0 (frozen) of feces or r, an improvement is seen in four ABC scales after treatment: ABC stereotypical behavior, ABC hyperactivity, ABC irritability, ABC lethargy/ social withdrawal (data not shown).

At a al FCT level of 6.0 Units/gram (fresh) or 9.0 (frozen) or greater in feces after treatment, there are increases in calorie , protein intake, meat., poultry, ﬁsh, fruit consumption, vegetable consumption, legume consumption ,carbohydrate consumption along with a beneﬁcial decrease in the glycemic index.

] Decreases in glycemic index are highly correlated with improvements in lethargy as measured on the ABC scale.

In one embodiment, the glycemic index of a subject treated with a composition described herein ses by at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a subject treated with a placebo. rmore, in another embodiment, a t experiences a decrease in lethargy as measured on the ABC scale. Such a decrease may be about 5%, about 10%, about 15%, about 20%, about %, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a subject treated with a placebo.

Provided herein is a method of improving the uptake of one or more vitamins and/or minerals in an autistic child, comprising administering to a subject in need f a composition described herein. In one embodiment, a subject to be d with such methods is autistic. In another embodiment, a subject to be treated is female.

In yet another embodiment, a subject to be treated is male. In another embodiment, uptake of one or more of Plant Based Vitamin A, Carotenoids (alpha and beta carotene), Vitamin K, Vitamin E, Vitamin C, um, copper, food folate, lutein, lycopene, magnesium, moisture content of foods, ium, phosphorus, sodium, polyunsaturated fatty acids, monounsaturated fatty acids, saturated fats, cholesterol, vitamin E, Vitamin K, and omine is improved by at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a subject treated with a placebo.

In another , provided herein is improving the quality of diet of an autistic child by increasing en essential vitamins and minerals: vitamins B6, B12, A (plant sources), C, E, K, along with Copper, Iron, Cholesterol, Niacin, Riboﬂavin, Thiamin, and Zinc, by administering to the child a composition described herein. In studies conducted by the t inventors, the increases in these vitamins and minerals were statistically significant (data not shown).

The chymotrypsin biomarker can also be a good indicator of subjects with physiological rition. Provided herein is a method of monitoring physiological malnutrition in a subject comprising measuring chymotrypsin concentrations in one or more body ﬂuids or tissues and comparing those levels to a baseline concentration or to levels in one or more healthy subjects.

All ic subjects at baseline were ed to have a lower overall caloric intake compared to subjects age-matched either subjects with a sedentary life style or an active life style. Provided herein is a method of ing caloric intake in an autistic subject, comprising administering to a subj ect in need thereof a composition described herein. In one embodiment, a subject treated with such methods exhibits improved caloric intake of at least about 5%, about 10%, about 15%, about 20%, about %, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a subject treated with a placebo.

Compositions described herein can be used to prevent or reduce the number of fractures in subjects with abnormal ﬂora in their guts (such as autistic subjects), and in other subject populations such as, for e, subjects who take antibiotics, who have Crohn’s disease, and who have a small and large intestinal disorder that s ﬁom damage inﬂammation necrosis or disease. tion or reduction of the number of fractures can be at least about 5%, about 10%, about 15%, about 20%, about %, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a subject treated with a placebo.

] Increased clotting disorders in autistic and other subjects has been observed due to deﬁciency in vitamin K and deﬁciency in serotonin transport from platelets. ed herein is a method of treating a clotting disorder in a subject, comprising administering to a subject in need thereof a composition described herein. In one embodiment, clotting is modiﬁed by at least about 5%, about 10%, about 15%, about %, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a subject treated with a placebo.

Potential measuring levels of gamma carboxylated proteins in the blood as a measure of vitamin K deﬁciency can be a novel ker for autism and other mal- nutritional ncies. As subjects with autism trated increased vitamin K intake, the carboxylation of certain glutamate residues can be essential to autism. ed herein is a method of decreasing Vitamin K intake in autistic subjects, comprising administering to a subject in need f a composition described herein. In one embodiment, a subject treated with such methods exhibits decreased Vitamin K intake of at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about %, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% ed to a subject treated with a o.

Also provided herein is a method of sing carboxylation of glutamate residues, comprising administering to a subject in need thereof a composition described herein. In one embodiment, a subject treated with such methods exhibits sed carboxylation of glutamate residues of at least about 5%, about 10%, about 15%, about %, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a subject treated with a placebo.

It appears that subjects with autism s an ongoing loss of overall caloric intake as well as the caloric intake of fat, protein, and carbohydrates. Enzyme replacement therapy reverses the loss of protein and fat caloric intake.

Provided herein is a method ofreversing protein loss and fat caloric intake in a subject, comprising administering to a subject in need thereof a composition bed herein. In one embodiment, a subject treated with such s exhibits decreased protein loss of at least about 5%, about 10%, about 15%, about 20%, about %, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a subject treated with a placebo.

In general, female subjects who are treated with a composition described herein who experience an increase in protein consumption, have an improvement in four ABC scales: ABC typical behavior, ABC hyperactivity, ABC irritability, ABC lethargy/ social awal. In one embodiment, provided herein is a method of increasing protein consumption in an autistic female child, sing administering to a female indiVidual in need thereof a composition described herein. In one embodiment, a female indiVidual d with such methods exhibits an improvement in four ABC scales of at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about %, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a female individual d with a placebo.

The present inventors identiﬁed that overall consumption of polyunsaturated fatty acids improved in a subject population treated with a composition bed herein when study participants achieved a study level ofFCT greater than 6.0 grams (unfrozen) or 9.0 units/ gram (frozen) in their feces (data not shown). In one embodiment, provided herein is a method of sing consumption ofpolyunsaturated fatty acids in a subject in need thereof, comprising administering to a subject a composition described herein. In one embodiment, consumption ofpolyunsaturated fatty acids increases by at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a subject treated with a placebo.

The present ors also identiﬁed that subjects treated with compositions described herein exhibited an increased consumption ein and fats, which seemed to correlate more favorably to improvements in irritability and hyperactivity on the ABC scale. In one embodiment, provided herein is a method of increasing consumption ofpolyunsaturated fatty acids in a subject in need f, comprising administering to a subject a ition described herein. In one embodiment, consumption ofprotein and fats ses by at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a subject treated with a placebo.

It appears that Asians improved to an even greater extent for ABC, c, ially everything overall. Provided herein is a method of treating an Asia subject for improving one or more les ofthe ABC scale, improving caloric intake, preventing or reducing the number of fractures in ts with abnormal ﬂora in their guts (such as autistic subjects), and in other subject tions such as, for example, subjects who take antibiotics, who have Crohn’s disease, and who have a small and large intestinal disorder that results from damage inﬂammation necrosis or disease, improve diet and weight, improve one or more of Connor’s DSM-IV attributes, or any ofthe other conditions/attributes described herein, comprising administering to an Asia subject in need thereof a composition described herein.

] Girls respond better to enzyme replacement therapy, as they tend to have more severe cases of autism. Provided herein is a method of treating autism in a female individual, sing administering to a female individual in need thereof a composition described herein. In one embodiment, a female individual treated with such methods exhibits a reduction in one or more symptoms of autism of at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a female individual treated with a placebo.

In one embodiment there can be a condition ofprotein calorie malnutrition in autistic subjects. The form of protein energy malnutrition in the autistic population is due to the selection of improperly ed diet due to the self-restriction that s from inability to digest protein. Indicators for malnutrition in the autistic population that can serve as a partial marker for autism (which would be conﬁrmed by additional conﬁrmation by the ABC test or other markers) include, for example: one or more of Anthropometry (for example: height for age (e.g., chronic malnutrition , stunting, eta), weight for age (e.g., protein energy rition), weight for height (e.g., acute malnutrition, wasting, eta), middle upper arm circumference, demi or arm span, knee height, g height, skin fold thickness, head circumference, edema, and body mass index); deﬁciencies in essential vitamins and minerals (other than Vitamin K); micronutrients; biochemical testing (e.g., Albumin, umin and/or Cholesterol); monitoring oral ; other enzyme deﬁciencies such as elastase and trypsin along with other enzymes.

Subjects with autism that have enzyme replacement therapy have statistically signiﬁcant ions in whole grains as well as approximately a 20% reduced intake in overall ydrates as a result of the enzyme replacement therapy over a twelve week period. ed herein is a method ofreducing whole grains and/or intake of carbohydrates, in an autistic child, comprising administering to a subject in need thereof a ition described herein. In one embodiment, a subject treated with such methods exhibits a reduction in one or more symptoms of autism of at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a subject treated with a placebo.

WO 03746 In one embodiment the compositions described herein can be used to treat autistic ts as it has been newly identiﬁed that many autistic subjects avoid eating protein. Overall protein intake doubles with enzyme replacement therapy and an approximate 15% increase in fat ption compared to subjects not treated with an enzyme over a 12 week period. Provided herein is a method of increasing protein intake in a subject, comprising administering to a subject in need thereof a composition described herein. In one embodiment, a subject treated with such methods exhibits a reduction in one or more ms of autism of at least about 5%, about 10%, about %, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a subject treated with a placebo.

In one embodiment, subjects having a history of allergies and treated with enzyme replacement therapy had a larger intake of ﬁber, calories, fat, n, and carbohydrates than autistic subjects treated with enzyme replacement therapy that did not have allergies. The methods described herein can be d as needed depending upon whether or not a subject to be treated has allergies.

In autistic subject given enzyme replacement therapy, the sed caloric intake did not result in an al increase in weight due to the overall improvement in the quality of their diets. The increase in quality of their diets had statistically signiﬁcant changes in the thirteen essential vitamins and minerals which are vitamins B6, B12, A, C, E, and K, along with Copper, Iron, Cholesterol, Niacin, Riboﬂavin, Thiamin, and Zinc.

Thus, in one ment, a subject d with any of methods described herein exhibits an improvement in caloric intake without causing an abnormal increase in weight or obesity.

] Compositions described herein can be administered with one or more additional agents. For e, in one non-limiting embodiment, provided herein is a method oftreating autism in a subject, comprising administering to a subject in need thereof a composition bed herein with ate enhancing therapy.

Provided herein is a method treating autism in a subject, comprising administering to a subject in need thereof a composition sing vitamin K in conjunction with glutamate enhancing therapy can be a novel treatment for autism.

Treatment can ﬁarther include an enzyme composition described herein.

A subject to be treated with a method described herein includes a subject that is between about 1 and about 25 years of age. In some embodiments, a subject is 2013/020183 from about 5 years to about 20 years of age, from about 2 years to about 10 years of age, from about 3 years to about 8 years of age, from about 10 years to about 15 years of age, from about 10 to about 20 years of age, or any range therebetween.

] Provided herein is a method for monitoring the Fecal Chymotrypsin level to select dosing of a composition herein for treatment of subjects with Autism. The concentration of fecal chymotrypsin may be measured using any conventional assay. In one embodiment, the method includes measuring the concentration of chymotrypsin in a sample obtained from an autistic child, comparing the concentration to one or more control values, and determining if additional treatment is needed. In one embodiment, a control concentration may be that of a subject known to not be autistic. In another embodiment, a l concentration may be that of a subject known to be autistic.

Fecal Chymotrypsin Level may be used to titrate dosage in order to tailor dosing for an optimal subject se by assessing the values of fecal chymotrypsin and the deltas between the concentration identiﬁed in a subject compared to the one or more controls (2'.e., difference between baseline and termination).

Dosing may be adjusted based on one or more ofthe following: weight, ne chymotrypsin level, instantaneous chymotrypsin level, time averaged chymotrypsin level, change in chymotrypsin level, change in chymotrypsin level per unit time, rate of change of chymotrypsin level per unit time (2nd derivative), cumulative dose to date, time averaged dosing over a given time , rate of change of dosing against rate of change in chymotrypsin level, derivative of rate of change of dosing t rate of change in chymotrypsin level.

Fecal chymotrypsin levels may be determined on an hourly, daily, weekly, bi-weekly, monthly, bi-monthly or yearly basis.

Other enzymes secreted in stools that may be equivalent or even less efﬁcacious markers may be also be measured in order to assess a subject’s state and determine the best course of treatment.

The present inventors have identiﬁed that, the more severe the autism diagnosed, the lower the ne fecal chymotrypsin level is found.

Furthermore, the lower the ne fecal chymotrypsin level, the r improvement is observed in the fecal chymotrypsin level and a corresponding greater improvement in the disease ing treatment with a composition described herein (data not shown).

] In one embodiment, a terminal FCT level of 6.0 Units/gram (fresh) or 9.0 (frozen) or greater of feces along with an FCT 3.5 or greater from baseline determination indicates an improvement in the subject being d.

In one ment, the level of hyperactivity and other symptoms of ADHD can be determined by the Conners-3 test.

In yet another embodiment, the s-3 subscales for hyperactivity can be compared to those on the ABC.

In yet another embodiment, the Conners scale can be utilized to determine if a change in behavior has occurred in subjects with ADHD and autism as hyperactivity is a co-morbid symptom found in autism.

In another embodiment, the attributes that can be measured utilizing the Conners-3 in subjects with autism are: restless or overactive behavior; ctivity; excitability and impulsiveness; failing to finish tasks; inattentiveness and ease of distraction; temper outbursts; ﬁdgeting; disturbances of other subjects; demands to be met immediately and ease of ation; ease and frequency of crying; and rapid and drastic mood changes. Each attribute is scored on a scale of 0-3 where 0 = never, seldom; l = occasionally; 2 = often, quite a bit; and 3 = very often; very frequent.

In one embodiment, the comparison of change in intake of ydrates as ed by the use ofthe block food screener and the Conners test for change in ctivity demonstrate that at all levels of carbohydrate intake change the subjects administered a composition described herein improved in their Conners scores over subjects administered the o over the course of 12 weeks.

In yet another embodiment, the changes the improvement in hyperactivity in subjects administered the enzyme composition may be due to the ement in carbohydrate digestion.

In yet another embodiment, the changes the improvement in hyperactivity in subjects administered the enzyme preparation may be due to the improvement in protein digestion as evidenced by an improvement in the n components ofthe carbohydrates.

In yet another embodiment, the enzyme preparation ns proteases, amylases, and lipases, thus, subjects administered the enzyme composition demonstrate improvement over subjects who are not administered the enzyme composition.

In one embodiment, the comparison of change in intake of carbohydrates as measured by the use ofthe block food screener and the Conners test for change in inattention demonstrate that at all levels of carbohydrate intake change the subjects stered a composition described herein improved in their Conners scores over subjects administered the placebo over the course of 12 weeks.

In yet another ment, the changes the improvement in inattention in subjects administered the enzyme preparation may be due to the improvement in carbohydrate digestion.

In yet another embodiment, the changes the improvement in inattention in subjects administered the enzyme preparation may be due to the improvement in protein digestion as ced by an improvement in the protein components ofthe carbohydrates.

In yet another embodiment, the enzyme preparation contains ses, amylases, and lipases, thus those administered the enzyme demonstrated improvement over subjects who are not administered the enzyme.

In yet r embodiment, a decrease in inattention was seen in subjects not administered the enzyme as their carbohydrate intake increases. In subjects administered a placebo, the inattention increases as the carbohydrate intake increases.

In yet another embodiment, the increase in carbohydrate intake without the concomitant replacement of enzyme, allows for the worsening ofthe inattention, most likely due to the inability to digest the protein in the ydrates (gliadan).

In yet another embodiment, as ydrate consumption increases, it was observed that inattention decreases in those administered Formulation l, and was observed to increase in subjects not administered the medication (e. g., a composition of Formulation 1).

In yet another embodiment, the se in carbohydrate intake t the concomitant replacement of enzyme, allows for the ing ofthe ntion, most likely due to the ity to digest the protein in the carbohydrates (gliadan).

In yet another ment, the PPVT and the EVT tests were both affected by the amount ofprotein intake following administration of a ition described herein. The PPVT and the EVT growth score changes are the measure ofthe amount of overall change in receptive and expressive language adjusted for the age of the child.

In one embodiment, the growth scores for both the EVT and the PPVT increased, demonstrating improvement in subjects administered the enzyme preparation.

In yet another embodiment, at the end 12 weeks the e of both the PPVT and the EVT growth scores ofthose administered a composition described herein remain signiﬁcantly better than subjects administered the placebo.

] In yet another embodiment, in both the EVT and the PPVT, subjects administered the placebo exhibit a worsening in their scores as the amount of protein subjects ingest per day at week 12 increases.

In yet another embodiment, an ement in scores is seen in the PPVT in subjects administered a composition described herein as the amount of protein that is ingested per day at week 12 increases.

] In yet another embodiment, the EVT the scores remain constant demonstrate large improvements across all levels ein intake per day at week 12.

In yet another embodiment, the instant ﬁndings represent the administration of a high protease formulation where at week 12 a signiﬁcant improvement in growth scores in both the PPVT to the EVT can be demonstrated.

Improvement in any one ofthe symptoms or outcomes may be measured according to any of the tests described herein or conventionally accepted in the art. For example, improvement may be at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95% or about 100% compared to a subject treated with a placebo (placebo). In another example, improvement may be at least about 2-fold, about 3-fold, about , about 10- fold, about 15-fold, about 20-fold, about 25-fold, about 30-fold, about 35-fold, about 40- fold, about 45-fold, about 50-fold, about 55-fold, about 60-fold, about 65-fold, about 70- fold, about d, about 80-fold, about 85-fold, about 90-fold, about 95-fold or about 100-fold ed to a subject treated with a placebo (placebo).

The following experiments describe ary procedures in accordance with the invention. It is to be understood that these experiments and corresponding results are set forth by way of illustration only, and nothing therein shall be construed as a limitation on the overall scope of the invention. By way of example, these studies demonstrate some ofthe unexpected improvements realized by the exemplary encapsulated enzyme preparations ofthe present disclosure. 100- 2013/020183 EXAMPLE 1: Increased flow properties and pourability of an exemplary encapsulated digestive enzyme preparation Before the exemplary methods and preparations ofthe present disclo sure is d, examination of an unprocessed, raw enzyme ation (Scientiﬁc Protein Laboratories (SPL) of Wanakee, WI) ed that it contained signiﬁcant variability in particle size and 20 irregular morphology, as shown in an electron micrograph of the particles (data not shown). Some crystalline salt particles are also visible. The raw enzyme does not pour as it clumps and is lt to measure due to the uneven surfaces, and jagged edges. The raw preparation is also not suitable for lipid encapsulation without ﬁthher processing because the raw product contains particles both too large and too small for proper encapsulation. The sieved enzyme while more uniform in size, continues to exhibit uneven surfaces and clumps while pouring.

The coated enzyme preparation may be ed following sieving and lipid coating of the raw material (data not shown). In this example, the morphology of particles is signiﬁcantly improved, with rounder surfaces. This leads to a non-dusty product with good ﬂow and organoleptic properties.

The morphology ofthe enzyme is now y improved due to the rounding ofthe surfaces, which leads to a product which is less dusty, does not aerosolize and has good ﬂow and improved leptic properties.

The size distribution of particles in the raw enzyme preparation is determined. In general, large particles (>40 mesh) and very small particles (<l40 mesh) are not suitable for proper encapsulation. In order to increase the ﬂow properties of the encapsulated pancreatic enzyme ation, the raw enzyme particles were sieved to include only particles of sizes 40-140 mesh, or about 106 to 425 s.

EXAMPLE 2: Stability of an exemplary encapsulated digestive enzyme preparation: temperature storage In a ﬁlrther ary embodiment, multiple types and weight tages of lipids were used to coat the sieved enzyme cores. Properties including mechanical strength, melting point, and hydrophobicity were taken into consideration in choosing a suitable lipid coating for the pancreatic enzyme. Multiple examples of lipid coatings were ed below and their physical appearances were examined under 25° C and at 40° C. Accordingly, lipids with a range ofphysical properties such as mechanical strength, melting point and hydrophobicity were evaluated for coating of the pancreatic 101- WO 03746 enzymes. In this example, it was found that the decreasing the g point or increasing the hydrophilicity of the coatings were not suitable for encapsulation e they resulted in t that would cake under accelerated storage stability conditions.

The sieved and encapsulated enzyme preparations made using hydrogenated soy oil, hydrogenated castor wax, and camauba wax all demonstrated good pouring and no caking.

Both the hydrogenated monoglycerides and the soy oil / monoglyceride blends demonstrated caking at the higher temperature. Therefore it is clear that the lower melting or more hilic coatings were not suitable for encapsulation because they resulted in a product that would cake under extended storage conditions as evidenced by our accelerated storage condition test at 40 degrees Centigrade.

Both the hydrogenated monoglycerides and the monoglyceride blends demonstrated caking at the higher temperature. Therefore it is clear that decreasing the melting point or sing the hydrophilicity of the coatings were not suitable for encapsulation because they resulted in a product that would cake under extended storage conditions as evidenced by our accelerated storage condition test at 40 degrees Centigrade.

EXAMPLE 3: An exemplary encapsulated ive enzyme preparation suitable for pancreatic enzymes: enzyme ty measured as a function of stability.

In a ﬁlrther embodiment, enzyme stability was determine according to the following method: For the accelerated test, standard ICH guidelines were used: the coated ations were placed in a plastic container, which was stored in a controlled humidity cabinet at 40°C and 75% relative humidity. tic activity was measured by grinding the coated enzyme preparations, dispersing in appropriate buffers, and testing for lipase activity.

The soy oil 80% appeared to impart the greatest amount of stability of all the , an effect that singly was greater for enzyme preparations stored in capped containers than in uncapped containers. Tests of ity for 75% relative humidity enzyme preparations stored at 40°C in open pans did not show significant differences in stability between coated and uncoated preparations. 102- EXAMPLE 4: An exemplary encapsulated digestive enzyme preparation suitable for pancreatic enzymes: enzyme activity and rate of release of multiple soy encapped pancreatic enzyme ] In a ﬁlI‘thGI' embodiment, encapsulates were ed according to the methods described below. The raw enzyme material was sieved to obtain particles smaller than 40 mesh but larger than 140 mesh, to remove ﬁnes, and to obtain a more uniform mixture more suitable for enteric coating.

The following preparations were made: (1) 70% active enzyme by weight, with a standard stable soy coating; (2) 80% active enzyme by weight, with a standard stable soy coating; and (3) 90% active enzyme by weight, with a standard stable soy coating.

] Activity in each encapsulated enzyme preparation was measured by ng the encapsulates, sing the ground material in appropriate buffers, and g for lipase activity.

As shown in Figure l, the enzyme activity in the coated preparations does not show any signiﬁcant loss of activity upon coating (decrease from 110 to 100% activity, normalized to stated enzyme activity of the raw enzyme material).

] Enzyme release was measured by suspending each encapsulate in a ution apparatus at pH 6.0 buffer for 30, 60, and 90 minutes (100 rpm, as per USP guidelines). As shown in Figure 2, all ulates show between 80-90% release at 30 and 60 minutes. At 90 minutes, the measured enzyme activity obtained with these preparations decreases.

EXAMPLE 5: An exemplary encapsulated digestive enzyme preparation suitable for pancreatic s: particle size of multiple soy oil encapped pancreatic enzyme In a ﬁlrther embodiment, preparations containing 70% or 80% active pancreatic enzyme by weight, encapsulated with soy oil were compared to raw atic enzyme material with respect to particle size, as shown in Figure 3.

All levels of lipid demonstrate an impact of particle size. The 80% PEC demonstrates the most uniform as none appear at the 200 mesh level.

EXAMPLE 6: An exemplary encapsulated digestive enzyme preparation suitable for pancreatic s: smell and taste Examination of exemplary encapsulated enzyme preparations containing 70%, 80% and 90% enzyme by weight was med to determine their taste and smell 103- WO 03746 when compared to SucanatTM and brown sugar, as well as ed to the raw enzyme.

The results are shown in the table below. SucanatTM is an organic whole food sweetener.

SUBSTANCE ODOR TASTE Brown sugar Yes Sweet SucanatTM No Sweet Raw Enzyme Meaty/smoky N/A 70% No No 80% No No 90% Slight Salty EXAMPLE 7: An exemplary encapsulated digestive enzyme ation suitable for pancreatic enzymes: manufacturing The ﬂow chart outlining a manufacturing process useful in making an enzyme preparation is shown in Figure 4.

Ingredients used in making a batch of an exemplary ulated pancreatic enzyme preparation included 20.0 lbs of sieved pancreatic enzyme and 5.0 lb. of hydrogenated vegetable oil, for e, soy oil.

The pancreatic enzyme concentrate was ﬁrst sieved through a 40 USSS mesh , and the material which passed through the mesh was retained. The retained material was then screened through a 140 USSS mesh screen (or the equivalent), and the material which did not pass through the mesh was retained as the sieved pancreatic enzyme material or particles.

In the encapsulation process, the appropriate coating material is charged to the melt pot, and brought to and maintained at 110° F for the spraying process. Any temperature that will provide appropriate consistency during the spraying process can be used. In some embodiments, the temperature is ﬁthher selected based on the melting points of the lipids used in the coating, and/or so that after contact of the sieved pancreatic enzyme material or particles with the g, the activity of the enzyme preparation remains about the same.

The liqueﬁed coating material is weighed and transferred to the spray pot.

The sieved pancreatic enzyme was added to the encapsulation manufacture vessel. The pancreatic enzyme les are encapsulated with coating al to the selected coating level. 104- WO 03746 The encapsulated material is screened with a 14 USSS mesh screen (or equivalent), and the material that passes through the screen is retained. Following sieving, the material is ted and samples are removed for y control (QC).

Iftwo sub-batches are to be blended, the loaded screened material is added to a suitable blender and blended for 7 to 10 s. Samples are obtained for ﬁnished product testing. The encapsulated material is bulk packaged and placed in quarantine pending test results. Upon achieving acceptance criteria, the ﬁnished product is released by the Quality group. Afterwards, the t can be shipped as ed.

Samples are collected for d product testing, including analytical testing and microbial assays, which can be tested over time.

EXAMPLE 8: An exemplary ulated digestive enzyme preparation suitable for pancreatic enzymes: packaging In yet another ﬁlrther embodiment, the stability of the enzyme is due in part to the encapsulation and in part to the trilaminar foil packaging. The ing demonstrates the packaging s for the single dose s/pouches.

First, ing manufacture the product is dispensed into clean, drums double lined with food-grade polyethylene bags, and the drums are sealed. If speciﬁcation criteria are met, the lot is then released from quarantine, and the material is then shipped to a suitable packager for placement into sachets for individual dosing to a subject.

For example a PD-73272 Printed Child Resistant (CR) Pouch consisting of 26# C18 Paper/ 7.5# LDPE/.0007” Aluminum Foil/15# with a Surlyn liner is utilized for packaging. Preferably pre-printed ﬁlm/foil, exterior printing will be with 1 color eye- mark on white background while in-line printing of lot number, expiration date and product code will also be in 1 color, black. Overall sachet dimension are: W 2.50” x H 3.50”. The sachet is sized to hold 900 mg of granules of Pancreatin lipid-encapsulated drug product with a tolerance % into a unit dose pouch/sachet. The ﬁnal product will have a protease activity ofnot less than 156 USP units/mg.

EXAMPLE 9: An exemplary encapsulated digestive enzyme preparation suitable for pancreatic s: dissolution The effect of the release of pancreatic extract complex from lipid encapsulated particles with soy oil was studied using particles with varying levels of lipid coating (expressed as % lipid coating per total le weight. The coating level was 105- varied from 10% to 30%. There was no signiﬁcant effect of lipid coating in this range on the release of pancreatic t complex in an aqueous environment from the particles over a 60-minute period. All formulations release over 80% ofthe enzyme within the ﬁrst 30 minutes following the tion of dissolution. Maximum release for the 90%, 80% and 70% particles was 85%, 88% and 83% respectively by 60 minutes.

The choice of 70% -90% ulated pancreatic enzyme preparation (active enzyme by weight) was selected on the basis of its release proﬁle, as suitable for release of the enzyme in the proximal small intestines where protein digestion by the protease component will take place.

Soy oil was selected as the lipid coating, for its lack of protein ents, and corresponding lack of antigenic properties, to minimize or eliminate the possibility of an allergic reaction to the lipid coating in treated ts and ts with autism.

The use ofthe 70-90% preparation increases pourability and ﬂow properties while ses aerosolization, which permits use of a sachet or pouch delivery system.

The addition ofthe trilamminar foil g insures that the le formulation will be stable, ortable, and will be delivered by a single unit dose mechanism.

The low lipase ation allows also for the safety by reducing the potential for colonic strictures, and enhances the utilization of the protease portion of the EXAMPLE 10: Biochemical biomarkers, and behavioral core and non-core symptoms The correlation between digestive enzyme deﬁciencies in autistic subjects was determined in subjects diagnosed with autism based on clinical (behavioral) symptoms. This correlation was also studied in subjects diagnosed with autism and a genetic co-morbidity. Following the l discovery that autistic subjects exhibited selfimposed protein dietary restrictions, studies were conducted which indicated that abnormally low levels of fecal chymotrypsin (PCT) is useﬁll as a biomarker for autism.

Fecal chymotrypsin may be assessed using conventional methods including, but not limited to those described herein, and commercially available kits (6.g. , Monotest Chymotrypsin; nger, Mannheim).

Infant feces are ted in a manner to keep them free from urine ination and mixed with water to obtain a weight by weight (w/w) mixture (6.g. 106- 1:4 w/w). This mixture is then mixed thoroughly to obtain a homogeneous suspension by homogenization or sonication. The feces are then diluted with a reaction buffer, described below, to obtain a fecal tration which, when added to a protease ate, hydrolyzes the substrate over a 5 to 60 minute period. Using such a method, for example, fecal chymotrypsin may be measured.

For the fecal chymotrypsin test, a stool sample is collected from a t.

Each stool sample can be analyzed using an enzymatic photo spectrometry analysis to determine the level of fecal chymotrypsin in the stool; in some cases the assay is med at 300 C, see, e.g: US. Pat. No. 6,660,831, incorporated by reference herein.

Alternatively, other methods, such as the colorimetric method, use of substrates, use of , and/or any other suitable method may be used to measure the fecal chymotrypsin levels. The levels of fecal chymotrypsin in the samples of a subjects suspected of or diagnosed as having autism are compared to the levels of fecal rypsin in subjects not suspected or diagnosed with autism to determine if the tested subjects exhibit lower fecal chymotrypsin values and to determine if a subjects would beneﬁt from the stration of a composition as described herein.

In addition, the number of autistic subjects responding to pancreatic enzyme replacement was also determined, based on biomarker measurements and clinical symptoms. Changes in the intestinal system as well as a change in the core symptoms of autism were examined.

Initial observations were based on observation of self-imposed dietary restriction by almost all subjects with . Multiple studies were then conducted to evaluate the ability of autistic subjects to digest n. A study of the physiology of protein digestion led to an examination of the gastrointestinal system’s cascade of digestive enzymes, especially those ed in protein degradation, such as chymotrypsin. As a measure of dysﬁlnction, it was determined that fecal chymotrypsin (FCT) levels in subjects suffering from autism were abnormally low.

This initial study was an exploratory one to determine if a small cohort of subjects with autism indeed would have abnormally low levels (<90) of fecal chymotrypsin (FCT). .

All 9 subjects with autism evidenced an abnormally low FCT level of below 7 Units/gram (Normal 2 9.0). This ation in a small set of subjects led to 107- ﬁarther ation of the potential for a physiological link to autism heretofore overed.

St_udy_2 Study 2 was undertaken to determine if a larger cohort of subjects (26 subjects) with autism also experienced abnormally low FCT levels. Levels of fecal elastase-1, another pancreatic digestive enzyme present at low amounts in pancreatic insufﬁciency, were also determined. Again, the levels ofFCT were abnormally low in 25 ofthe 26 subjects, falling at 8 U/g or below. One child had an FCT level of 9 U/g. On the other hand, all of the subjects had normal levels of fecal elastase-l.

Study 3 In Study 3, FCT levels were ined in 46 subjects aged 2 years to 14 years of age, 25 with autism and 21 without autism, The data demonstrated that subjects with autism had ally low FCT levels and subjects who did not have autism had normal FCT levels, of 12 U/g or higher. The s are ized in Figure 7. The top line in Figure 7 shows the FCT levels in subjects who did not have autism, while the bottom line shows the FCT levels in subjects who did have autism.

Study 4 In Study 4, FCT levels were determined for 463 subjects aged 2 years to 8 years of age, 266 diagnosed with autism and 197 diagnosed without autism, in a multi- off1ce physician-conducted study. The data showed that the subjects with autism had abnormally low fecal chymotrypsin levels and subjects who did not have autism had normal levels of fecal chymotrypsin.

The data is summarized in the table below.

Mean Fecal Chymotrypsin Levels in Subjects with and without Autism Total numbers of subjects 266 197 Mean FCT (U/g) 4.4 23.2 Total Subjects with al Levels ofFCT 203 3 % (p<0.001) 76.34% 1.50% Total Subjects with Normal Levels ofFCT (p <0.01) 63 194 % 23.68% 98.50% 108- Chymotrypsin is a pancreatic enzyme. Chymotrypsin is a serine protease and is unique in that it cleaves only ial amino acids during the digestive process. cally, chymotrypsin s the peptide bond on the carboxyl side of ic amino acids. A lack ofprotein digestion as evidenced by abnormal FCT levels leaves the child with a dearth of amino acids available for new protein synthesis. Without sufﬁcient levels of essential amino acids, new proteins required for various bodily ons cannot be synthesized. For example, a shortage or lack of proteins involved in neurological processes can then give rise to symptoms of autism.

Chymotrypsin cleaves speciﬁc amino acids which are not cleaved by the other protease. In speciﬁc it cleaves the essential amino acids: phan, methionine, phenylalanine, and leucine, and the semi essential amino acid tyrosine. The two other major proteases do not cleave these essential amino acids and therefore the lack of chymotrypsin ty in the small intestine regardless ofwhy it is low will leave a subject with a lack of these amino acids. Other very low by volume proteases carboxypeptidase A and B cleave minute amounts of some ofthese amino acids, but not ent quantities to make up the difference.

Study 5 In Study 5, FCT levels were determined for 320 subjects aged 2 years to 18 years of age, 64 with autism, 64 with ADD. 64 with ADHD, 64 with known genetic conditions, and 64 normals (no known conditions). The data showed that the subjects with autism, ADD and ADHD exhibited abnormally low levels ofFCT compared to the subjects with known genetic ions and normal subjects. FCT data were ed during a multi-physician ofﬁce trial of age-matched subjects with multiple conditions.

Figure 8 depicts FCT levels in separate groups of subjects aged 6 years to 18 years who have Autism, ADHD (Attention Deﬁcit Hyperactivity Disorder), ADD ( Attention Deﬁcit Disorder), known c disorder also diagnosed with autism, or no known condition (normals).

The two upper lines in Figure 8 correspond to FCT levels in subjects without any known condition and subjects with known co-morbid conditions (genetic and others). The three bottom lines correspond to FCT levels in the subjects with autism, ADD and ADHD.

The Autism, ADD, and ADHD subjects had signiﬁcantly lower levels FCT than subjects without any known condition, or subjects with a known c co- morbidity or traumatic condition (p <0.01). 109- Study 6 In Study 6, 42 tched subjects, 25 with autism, and 17 without autism or other co-morbid condition, were examined using a stool test for the presence of multiple pathogens as well as markers of gastrointestinal dysﬁlnction, including FCT levels. The subjects with autism had a larger number of stool pathogens present as well as ally low FCT levels.

This small pilot study was undertaken to examine the gastrointestinal ﬂora of ts with autism versus subjects without autism. Multiple markers of gastrointestinal health were examined to determine if there is an abnormal gastrointestinal presentation in these subjects.

Forty two (42) subjects aged matched 25 with autism and 17 without autism or other bid condition were screened using a stool test for the presence of multiple pathogens as well as markers of Gastrointestinal dysﬁlnction. Other GI pathogens or stool markers known to those of skill in the art can also be tested as a marker of GI dysﬁanction. The table below shows the incidence ofpresence of a GI en or other stool marker.

Incidence of the Presence of Pathogens and other Stool s Representing Gastrointestinal Dysfunction AUTISM % TOTAL NOT % TOTAL AUTISM LOW PCT 25 100% 0 0% C. dz'ﬁ‘zcz'le 15 60% l 6% antigen Fecal Elastase 0 0% 0 0% <200 H. pylori antigen 17 67% 0 0% E. histolytica 8 32% 0 0% antigen Giardz'a antigen 9 36% l 6% Yeast overgrowth 4 l6% 0 0% Cryptosporz'dium 9 36% l 6% N = 25 N = 17 110- 2013/020183 The presence ofpositive stool markers in the subjects with autism, including low levels of fecal chymotrypsin indicated additional gastrointestinal problems in subjects with autism.

Example 11: Randomized Double Blind Placebo Controlled Trial of high Protease Enzyme Formulation in Subjects With Autism Subjects to be treated (Formulation l or placebo) were diagnosed with autism. Subjects were administered Formulation 1 ising pancreatin) or a placebo as a powder taken three times a day with food.

The clinical trial was an interventional study with parallel assignment that was randomized. Primary outcome measures ed evidence of changes in behavior scales and physical ms of autism at baseline, 14 days, 30 days, 60 days, and 90 days after treatment commenced.

Secondary Outcome Measures: other key measures of behavior and quality of life associated with autism were assessed at baseline, 14 days, 30 days, 60 days, and 90 days after treatment cement.

One hundred eighty two subjects were enrolled in the study. The two arms ofthe study were as s: Assigned Interventions Active Drug: FORMULATION l Comparator: 1 Single unit dose powder of active substance (Formulation l) Formulation 1 administered 3 times per day for 90 days Placebo Drug: Placebo Comparator: 2 Single unit dose powder ofnon-active substance administered 3 Placebo times per day for 90 days powder Eligibility ts seeking treatment were administered questionnaires and tests to determine the nature and ty of .

A ges Eligible for Study: 3 years to 8 years of age lll- Genders Eligible for Study: ‘ ccepts Healthy Volunteers: Inclusion criteria for subjects to enroll in the study ed that the subject met the current Diagnostic and Statistical Manual for Mental Disorders (DSM-IV-TR) diagnostic criteria for autistic disorder (AD) Exclusion criteria for ts to be excluded from the study included the following parameters: 1. Subject weighing less than (<) 11 kg (24.2 lbs.); 2. Demonstrated previous allergy to porcine (pork) products; 3. Previous history of severe head trauma or stroke, seizure within one year of entering study or uncontrolled ic disease; 4. Diagnosis of: HIV, cerebral palsy, endocrine er, pancreatic disease; ] 5. Within 30 days of starting the study, certain supplementation, chelation or dietary restriction (a 30 day washout period would be required for inclusion); 6. Use of any stimulant medication must be discontinued 5 days prior to entering the study; and 7. t must have a stable dose of SSRI's for at least 30 days.

Locations: The clinical trials were conducted at 19 locations throughout the United States.

Example 12: Clinical Trial of Formulation 1 in Subjects with Autism Autism is currently a signiﬁcant cause of disability in the pediatric tion. Formulation l is based upon the observation that many subjects with autism do not digest protein. Formulation l is an enzyme composition that is designed as a powder taken three times a day. ation l is a composition as described as in Example 8, where the ition comprises a soybean oil coated pancreatin granule comprising at least 156 USP units per mg. The composition is administered in USP Units per 900 mg dose. It is formulated to be released in the small intestine to enhance protein digestion thus increasing the availability of essential amino acids. The purpose of this study is to determine efficacy of ation l in treating the core symptoms of autism.

Subjects to be treated (Formulation l or placebo) are sed with autism. Subjects are stered Formulation l or a placebo. 112- The clinical trial is an interventional study with parallel assignment that was randomized. The endpoint classiﬁcation assessed during the trial is to ine treatment efficacy of the subjects with Formulation 1.

Primary Outcome Measures to be assessed include evidence of changes in behavior scales associated with the core ms of autism at baseline, 4, 8, 12, 16, 20, 24, 36, 60, 72, 84, 96, 108, 120, 132, 144, 156, 168, and 180 weeks oftreatment.

Secondary Outcome Measures to be assessed include other key measures vior and y of life associated with autism at baseline, 4, 6, 20, 24, 36, 48, 60, 72, 84, 96, 108, 120, 132, 144, 156, 168, and 180 weeks tment.

One hundred seventy (170) subjects are enrolled in the study and treated according to the following arm: Assigned Interventions Experimental: 1 Drug: Formulation 1 Formulation 1 Single unit dose powder of active substance (Formulation 1) administered 3 times per day for 90 days Eligibility Subjects seeking treatment undergo a questionnaire and tests to ine the nature and severity of autism. . ges Eligible for Study: 9 years to 12 years of age s Eligible for Study: ‘ ccepts Healthy Volunteers: Inclusion criteria for subjects to be included from the study included the following parameters: 1. Meets the current Diagnostic and tical Manual for Mental Disorders (DSM-lV-TR) diagnostic criteria for autistic disorder (AD). 2. Ongoing 00102 Protocol requires tion of 00101 Protocol. 3. Now recruiting subjects directly into 00102 Protocol.

Exclusion criteria for subjects to be excluded from the study included the following parameters: 1. Ongoing study required subjects to be 3-8 years old weighing < 11 kg (24.2 lbs.), and achieving ages 9-12 years old weighing < 22 kg (48.4 lbs.). 113- 2. Newly recruited subjects must be between ages 9 - 12 years old weighing < 22 kgs (48.4 lbs.). 3. Demonstrated previous allergy to e (pork) products. 4. Previous y of severe head trauma or stroke, seizure within one year of ng study or uncontrolled systemic disease. 5. Diagnosis of: HIV, cerebral palsy, endocrine disorder, pancreatic disease. 6. Within 30 days of starting the study, certain supplementation, chelation or dietary restriction (a 30 day washout period would be ed for inclusion). 7. Any use hotropic medications, stimulants, or SSRI's must be discontinued for 30 days prior to entrance.

Locations: clinical trials will be conducted at 19 locations throughout the United States.

Study 1A Two hundred ninety eight (298) subjects were ed for autism by the DMS-IV criteria as well as by the SCQ and the ADI-R stic tests. Once they were determined to have autism, they were tested for their fecal chymotrypsin .

] Once they were determined to have autism by the above aforementioned tests, and found to have low FCT levels (<l2.6 U/g of frozen stool) they were randomized and assigned to one oftwo parallel treatment groups: one administered the high protease enzyme composition (Formulation l) as described herein ,or a placebo.

Ongoing study required subjects to be 3-8 years old weighing >11 kg (24.2 lbs.). ation l or placebo was stered three times a day with food.

Formulation l is described herein as a high protease enzyme composition (the medication).

One hundred eighty-two (182) subjects were randomized. The clinical trial is an interventional study with parallel assignment that was randomized and blinded. The endpoint classification assessed during the trial was undertaken to determine treatment efﬁcacy of subjects with the high protease enzyme product described herein ( the medication) ,versus subjects administered the placebo.

FCT at Baseline FCT at week 12 114- FCT at Baseline FCT at week 12 In this study, the changes from baseline between week 0 (baseline) and week 12 for fecal chymotrypsin levels were measured. Subjects administered the medication were supplemented with active chymotrypsin, and subjects who were stered o were not supplemented with chymotrypsin.

Figure 15 shows the changes in fecal chymotrypsin levels from baseline in subjects administered the medication versus subjects administered the o.

Chymotrypsin levels improved signiﬁcantly over 12 weeks acement in the trial. The change of 1 demonstrated by the placebo is within the standard deviation ofthe test.

Subjects on placebo who did not receive chymotrypsin replacement did not e signiﬁcantly over the trial. A p value of <0.03 demonstrates cance over a 12 week period.

] This demonstrated that the chymotrypsin was replaced in subjects who received the medication and that those who received placebo did not receive replacement Study 2A The same cohort of subjects as outlined in study 1A was used in Study 2A. ts were screened for autism. The medication or placebo was administered three times a day with food. The medication is described herein as a high protease enzyme (Formulation 1).

Stool changes in pH were measured in both subjects administered the medication and in subjects administered the placebo As an increase in pH (more alkaline) occurs it is pathagneumonic for an increase in n digestion. As the maines present as a byproduct of the protein digestion are present it makes the stool more alkaline.

The pH ofthose administered the medication increased to an average of 0.03 and the stool pH of ts administered the placebo actually had a stool pH decrease by 0.16. The graphic depiction of the changes can be seen in Figure 16. The pH changes over the trial were sed in subjects who received enzyme replacement and subjects receiving the placebo lost pH change. 115- pH Levels at week 12 ations with calcium, copper and vitamin C are provided in the following table, There were positive robust signiﬁcant correlations between subjects administered Formulation l and calcium and vitamin C intakes , copper at week 12.

STUDY 3A The same cohort of subjects as outlined in study 1A was used in Study 3A.

The subjects were screened for autism. The medication or placebo was administered three times a day with food. The medication is described herein as a high protease enzyme composition (Formulation 1).

] One hundred eight two (182) subjects were randomized. The clinical trial is an interventional study with parallel ment that was randomized and blinded. The endpoint classiﬁcation assessed during the trial was undertaken to determine treatment efﬁcacy of subjects with the high protease enzyme composition described herein (Formulation 1), versus subjects administered the placebo.

Primary Outcomes assessed were the fore mentioned les of the Aberrant or Checklist. The total ABC was also assessed. Assessments were taken at time points of 12, 24 and 48 weeks. Weeks 0 to 12 were the medication versus the placebo, and weeks 24 and 48 were changes from baseline where all ts are stered the medication.

The outcome of this study was the improvement from baseline on the 5 les of the ABC Aberrant Behavior Checklist observed in subjects treated with Formulation 1 compared to the placebo.

Formulation 1: Improvement in: 12 week (placebo 24 weeks 48 weeks adjusted) Irritability 9 27 34 Lethargy l l 36 48 Hyperactivity l l 25 27 Stereotypy l l 31 38 116- The table demonstrates the changes in total ABC score from baseline at 12, 24, and 48 weeks during the study.

Each time point is characterized by the percentage change from baseline.

At the week 12 time point the percentage change is demonstrated as a o adjusted outcome, where by the change on placebo is subtracted by the change on the assessment in subjects administered the medication.

For those skilled in the art, placebo adjusted changes from baseline are standard ways to assess change between the two groups: medication versus placebo.

When there is a positive change, (sign is positive) the medication had a greater affect on the e change than the placebo. Should the change be negative the outcome is better in the placebo After 12 weeks, it is apparent that subjects administered the medication improve compared to those stered the placebo.

] Improvement appears to continue through week 48. In subjects whose symptoms are never thought to change over the course of their lifetime, the ability to see this magnitude in change could not have been anticipated.

Ofnote, the subscales of social withdrawal/lethargy, and hyperactivity/non-compliance are known as reciprocal scales. When hyperactivity increases, social withdrawal and lethargy are decreased. The opposite is true as well. The fact that both subscales decreased is significant as the changes demonstrate that there is a non-sedating effect of the medication, and a dating ch to the problem.

Further ofnote is the fact that all les have a large improvement over 12, 24 and 48 weeks. This is an unexpected ement both in the fact that it is all les and also the fact that the total ABC demonstrates ement.

STUDY 4A The PPVT and the EVT were administered to the subjects in the study. In the same cohort of subjects as outlined in study 1A.

The subjects were screened for autism. The tion or placebo was administered three times a day with food. The medication is described herein as a high protease enzyme (Formulation l). 117- WO 03746 One hundred eighty two (182) subjects were randomized. The clinical trial is an interventional study with parallel assignment that was randomized and blinded. The endpoint classiﬁcation assessed during the trial was undertaken to ine treatment efﬁcacy ofthe subjects with the high protease enzyme composition described herein (Formulation 1), versus subjects administered the o.

In normally developing subjects the EVT and the PPVT should demonstrate similar growth. The growth scales seen over a 12 month period should keep pace with one another. In the case of neurologically or otherwise ed subjects the scales will often not keep pace with one another.

Further the amount of growth (growth scores) demonstrated over a 12 month period should range from 8-10 points on both the EVT and the PPVT, depending upon age. In the ages 3-8 years range the growth score should be imately 8.

— PPVT Mean Changes In these PPVT results the growth scores for subjects on the medication exceeded subjects on the placebo. Growth scores are adjusted for age and for standardization of scores across the entire study (See Figure 17).

] Additionally subjects on the medication made fewer errors; whereas subjects on the placebo made signiﬁcantly more errors. This increase in error rate may signify an increase in ctivity or an increase in inattention, compared to subjects on the composition of ation 1.

The EVT was administered to the same group of subjects as the PPVT.

The EVT scores demonstrate a large difference between subjects administered the medication and subjects administered the placebo (See Figure 18).

There was also a reduction in the number of errors in subjects administered the medication compared to subjects administered the placebo The growth scores demonstrate a vast improvement in subjects administered the medication versus subjects administered the placebo Ofnote the growth scores seen in subjects administered the medication in 12 weeks are more than half ofwhat would be expected in a ly ping subjects 118- in 52 weeks. This increase in expressive language is a profound change in a subject with autism.

Also ofnote is the fact that there is a larger gain in growth scores in the EVT seen in ts administered the medication versus subjects administered the tion in the PPVT. This is not generally seen in normally ping subjects.

EVT Mean Changes STUDY 6A The Block food screener was administered to subjects in the study. In the same cohort of subjects as outlined in study 1A were assessed in the present study.

Subjects were screened for autism. The tion or placebo was administered three times a day with food. The medication is described herein as a high se enzyme composition (Formulation 1).

One d eighty-two (182) subjects were randomized. The clinical trial is an interventional study with el assignment that was randomized and blinded. The endpoint classiﬁcation assessed during the trial was undertaken to ine treatment efﬁcacy of subjects with the high se enzyme composition described herein lation 1), versus subjects administered the placebo.

The food screener was administered at baseline, weeks 2, 4, 8, and 12.

The following are various correlations seen between the food intake and changes seen on the various scales.

Figure 19 illustrates EVT mean standard score change as a ﬁanction of protein intake (g) at week 12.

Secondary Outcome Measures to be assessed included other key measures ofbehavior and quality of life associated with autism at baseline, 4, 8, l2, 16, 20, 24, 36, 48, 60, 72, 84, 96, 108, 120, 132, 144, 156, 168, and 180 weeks oftreatment.

ABC inappropriate speech percentage changes by week are provided in the following table: 119- ] ABC subscale change as a ﬁanction of subjects eating 50g+ daily protein at week 12 is provided in the ing table: ABC Subscale Formulation 1 o p Value Irritability -3 .38 1.61 .0381 Lethargy -5.70 -l.44 .0866 Hyperactivity -5.95 -0.90 .0392 Stereotypy -2.4l 1.17 .0055 TotalABC -l8.ll -0.l2 .0078 Conners Subscales Carbohydrate Change (g) >0 at week 12: Formulation 1 Placebo Hyperactivity -3 .07 -l .30 Conduct Disorder -l .77 -0.23 Oppositional Deﬁant -l .29 -0. 12 Global Impression -2.05 -l .24 Inattention -3 .55 -l .74 Hyperactivity -5 .27 -l .99 Learning Problems -2.69 -0.32 Aggression -2. 19 -0.47 When there is an increase in the amount of carbohydrates ingested >0g, there is a greater ement in subjects administered the drug over subjects administered the placebo.

The ing observations were made over the course ofthe trials: Fecal Chymotrypsin Change ated with changes in vitamin K and lutein.

—Formulation 1 Correlation Peabody Picture Vocabulary Test (PPVT) — PPVT Mean Changes 120- —Expressive Vocabulary Test (EVT): EVT Mean Changes Standard Group Ceiling Errors Score While preferred embodiments have been shown and bed herein, it will be obvious to those skilled in the art that such embodiments are provided by way of example only. Numerous variations, changes, and substitutions will now occur to those skilled in the art. It should be understood that various alternatives to the embodiments described herein can be employed. It is intended that the following claims deﬁne the scope of the ments and that methods and structures within the scope ofthese claims and their equivalents be d thereby. 121-

Claims

1. Use of a composition that comprises a protease, an amylase, and a lipase for the cture of a ment for the treatment of malnutrition as a result of self-imposed dietary restriction in a subject exhibiting an Autism Spectrum Disorder (ASD), wherein the medicament is formulated for administration to a subject two or more times a day with food and wherein upon administration of the medicament to a subject, the subject has an increase in a total daily fat, ydrate and/or vitamin intake (by weight) in comparison to intake before administration.

2. The use of claim 1, wherein an improvement in the ASD after stration of the medicament is at least 1-fold greater than in a subject stered a placebo.

3. The use of claim 1, wherein an improvement in the ASD after administration of the medicament is at least 2, 3, 4, or 5-fold greater than in a subject stered a placebo.

4. The use of claim 1, wherein the subject exhibits a 10% or greater improvement in the ASD after administration of the medicament in comparison to before the subject was administered the medicament.

5. The use of claim 1, wherein the subject exhibits greater than a 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, or 100% improvement in the ASD after administration of the medicament.

6. The use of claim 1, wherein the total daily fat, carbohydrate, or vitamin intake (by weight) by the subject increases ing administration of the medicament in comparison to total daily fat, carbohydrate, or vitamin intake by the t before administration of the medicament.

7. The use of claim 1, wherein the subject has a greater increase in the total daily fat, carbohydrate, or vitamin intake (by weight) ing administration of the medicament in comparison to a subject exhibiting the ASD following administration of a placebo.

8. The use of claim 1, wherein the greater the amount of the total daily fat, ydrate, or vitamin intake (by weight) consumed by the t after stration of the medicament the greater the subject’s improvement in the ASD.

9. The use of claim 7 or 8, wherein the total daily fat, carbohydrate, or vitamin intake (by weight) consumed by the subject is measured before the subject was administered the medicament and at about 2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 24, 36, 48, or 52 weeks after administration of the medicament begins.

10. The use of claim 1, n the subject has a greater increase in the total daily vitamin intake (by weight) following administration of the medicament in comparison to a subject exhibiting the ASD following administration of a placebo.

11. The use of claim 1, wherein the subject has a greater increase in the total daily carbohydrate intake (by weight) following administration of the medicament in comparison to a subject exhibiting the ASD following administration of a o.

12. The use of claim 1, wherein total daily calories consumed by the t increases after administration of the medicament in comparison to total daily calories consumed by the subject before administration of the medicament.

13. The use of claim 12, n the more total daily calories the subject consumed after administration of the medicament, the greater the subject’s ement in the ASD.

14. The use of claim 13, wherein a total amount of daily calories consumed by the subject is measured before administration of the medicament and at about 2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 24, 36, 48, or 52 weeks after administration of the medicament .

15. The use of any one of claims 1-14, wherein the subject further exhibits an improvement of a symptom of an ASD sing hyperactivity, attention, irritability, agitation, obsessive compulsive behavior, lack of eye t, inappropriate speech, lethargy, hypersensitivity, stereotypy, difficulties in toilet training, non-compliance, aggression, impulsivity, conduct disorder, oppositional defiance, social withdrawal, or a combination thereof, after administration of the medicament.

16. The use of claim 15, wherein the subject’s improvement in the ASD is measured on an nt Behavior Checklist (ABC) scale.

17. The use of claim 16, wherein the subject’s improvement in the ASD is measured as a total nt Behavior Checklist (ABC) score.

18. The use of claim 1, wherein total daily calories consumed by the subject administered the medicament is about the same as the subject consumed prior to administration of the medicament.

19. The use of claim 1, wherein total daily calories consumed by the subject administered the medicament is about the same as a subject administered a placebo for the same length of time.

20. The use of claim 1, wherein the subject ts an ement in carbohydrate intake of at least 3-10 grams per day after administration of the medicament.

21. The use of claim 20, wherein the subject ts an ement in carbohydrate intake of at least 5 grams per day after administration of the medicament.

22. The use of any one of claims 1-21, n a Block Food Screener is used to measure food intake.

23. The use of any one of claims 1-21, wherein a Block Food Screener is used to measure nutrient intake.

24. The use of any one of claims 1-21, wherein a Block Food Screener is used to measure the quantity of food intake.

25. The use of any one of claims 1-21, wherein a Block Food Screener is used to measure quality of food intake.

26. The use of claim 15, wherein the subject has an improvement in hyperactivity by 12 weeks after administration of the ment in comparison to a subject administered a placebo.

27. The use of claim 26, n hyperactivity is measured using a Conners test.

28. The use of claim 26 or 27, wherein a subject administered the medicament shows increased carbohydrate intake at week 12 in comparison to before the medicament was administered.

29. The use of claim 15, wherein the subject exhibits an improvement in attention by 12 weeks after administration of the medicament in comparison to a subject administered a placebo.

30. The use of claim 29, wherein attention is measured by a Conners test.

31. The use of any one of claims 1-30, wherein the subject has a more ne stool pH after administration of the medicament than prior to administration of the medicament.

32. The use of claim 31, wherein the t has a more alkaline stool pH after at least four weeks of administration of the medicament than prior to administration of the medicament.

33. The use of any one of claims 1-32, wherein the subject has a more alkaline stool pH after administration of the medicament than a subject administered a placebo.

34. The use of claim 33, wherein the t has more alkaline stool pH after at least four weeks of administration of the medicament than a subject administered the placebo.

35. The use of any one of claims 1-34, wherein the subject has an al fecal rypsin level before administration of the medicament.

36. The use of claim 35, wherein the subject has a fecal chymotrypsin level of less than 13 U/g as ed in a frozen stool sample before administration of the medicament.

37. The use of claim 36, wherein the t has a fecal chymotrypsin level of less than 12.6 U/g as measured in a frozen stool sample before administration of the medicament.

38. The use of claim 35, wherein the subject has a fecal chymotrypsin level of less than 10 U/g as measured in a fresh stool sample before administration of the medicament.

39. The use of claim 38, n the subject has a fecal chymotrypsin level of less than 9 U/g as measured in a fresh stool sample before administration of the ment.

40. The use of any one of claims 1-39, wherein the t has an increased fecal rypsin level after administration of the medicament.

41. The use of any one of claims 1-40, wherein the subject has an increased fecal chymotrypsin level after at least 12 weeks of administration of the medicament.

42. The use of claim 15, wherein improvement in the ASD further comprises a decrease in a number of incidents or a severity of hyperactivity, irritability, agitation, obsessive compulsive behavior, lethargy, hypersensitivity, stereotypy, non-compliance, aggression, impulsivity, conduct disorder, oppositional defiance, social withdrawal, or a combination thereof, in the subject after administration of the medicament.

43. The use of any one of claims 1-42, wherein an improvement in the ASD further comprises an increase in a number of nts or duration of eye contact after administration of the medicament.

44. The use of any one of claims 1-42, wherein an ement in the ASD further comprises an increase in a number of incidents, articulation or vocabulary of the subject’s speech after administration of the medicament.

45. The use of any one of claims 1-42, wherein an improvement in the ASD further comprises an improvement in toilet training after administration of the medicament.

46. The use of any one of claims 43-45, wherein the improvement is exhibited by the subject stered the ment and is greater than a subject administered a placebo.

47. The use of any one of claims 1-46, wherein a subject administered the medicament further has an improvement in overall health.

48. The use of any one of claims 1-46, wherein the subject administered the medicament further has a decrease in the number or severity of infections, or a decrease in the number or severity of allergic incidents, after administration of the medicament in comparison to before the subject was stered the medicament.

49. The use of any one of claims 1-46, wherein the subject administered the medicament further has a decrease in the number or ty of infections, or a decrease in the number or severity of allergic incidents, after administration of the medicament in comparison to a subject administered a placebo.

50. The use of any one of claims 1-49, wherein the subject is diagnosed as having an ASD before administration of the medicament.

51. The use of claim 50, wherein the subject is sed as having the ASD by a DSM-IV, a SCQ, or a ADI-R .

52. The use of any one of claims 1-51, wherein the Autism Spectrum Disorder is Autism.

53. The use of claim 15, n the symptom of the ASD is measured using an Aberrant Behavior Checklist (ABC) scale, a Conners test, an Expressive Vocabulary Test (EVT), a Peabody Picture Vocabulary Test (PPVT), a Social Communications Questionnaire (SCQ), an ADI-R test, or a DSM-IV test.

54. The use of claim 53, wherein the EVT is an EVT-2 test.

55. The use of claim 53, wherein the PPVT is a PPVT-4 test.

56. The use of claim 15, wherein hyperactivity is ed by a Conners test.

57. The use of claim 56, wherein the Conners test is a Conners-3 test.

58. The use of claim 57, wherein the Conners test is a Conners-3 test and ctivity is measured by comparing a s-3 test result with a hyperactivity result measured on an ABC scale.

59. The use of any one of claims 1-58, wherein one or more ms of the ASD are measured prior to administration of the medicament.

60. The use of any one of claims 1-58, wherein one or more symptoms of the ASD are ed after, or during, administration of the medicament.

61. The use of any one of claims 1-60, wherein one or more ms of the ASD are measured one or more times after administration of the medicament for 1, 2, 3, 4, 8, 12, 16, 20, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 70, 74, 78, 82, 86, or 90 weeks.

62. The use of any one of claims 1-61, wherein upon administration of the medicament, improvement in the ASD is observed for at least 2, 3, 4, 8, 12, 16, 20, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 70, 74, 78, 82, 86, or 90 weeks.

63. The use of any one of claims 1-61, wherein upon administration of the medicament, improvement in the ASD is observed for at least one week.

64. The use of any one of claims 1-63, wherein upon administration of the medicament, the subject exhibits a reduction in a number, severity, or number and severity of seizures compared to a subject administered a placebo.

65. The use of any one of claims 1-64, n the medicament is formulated for daily administration.

66. The use of any one of claims 1-64, wherein the medicament is formulated for stration 4, 5, 6, 7, 8, 9, 10, 11, or 12 times a day.

67. The use of any one of claims 1-64, wherein the medicament is formulated for administration twice a day, or three times a day.

68. The use of any one of claims 1-67, wherein the medicament is formulated for administration for at least 12 weeks.

69. The use of any one of claims 1-67, wherein the medicament is formulated for administration for at least 3-6 months, 6-12 months, 12-18 months, or 18-24 months.

70. The use of any one of claims 1-67, wherein the medicament is formulated for administration for at least 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 years.

71. The use of any one of claims 1-70, wherein the composition comprises a mixture of proteases comprising n and chymotrypsin.

72. The use of any one of claims 1-71, wherein the composition is pancreatin.

73. The use of claim 72, wherein the composition is a solid form of pancreatin.

74. The use of claim 72, wherein the composition is a crystalline form of pancreatin.

75. The use of any one of claims 1-74, wherein the medicament does not e a sedating effect; or wherein the medicament does not produce an increase in dizziness, Parkinson’s disease symptoms, dystonia, akathisia, somnolence, fatigue, extrapyramidal disorders, tremor, or drooling.

76. The use of any one of claims 1-75, wherein the composition further comprises a coating.

77. The use of claim 76, n the coating is an enteric g.

78. The use of claim 76, wherein the coating comprises a lipid, a lipid mixture, a blend of lipid and emulsifiers, or a polymer.

79. The use of claim 78, wherein the coating comprises the lipid, and n the lipid comprises a soy lipid.

80. The use of any one of claims 76-79, wherein the g masks the task, smell, or taste and smell of the composition.

81. The use of claim 77, n the c coating comprises hypromellose phthalate, dimethicone 1000, dibutyl phthalate, or a combination thereof.

82. The use of any one of claims 76-81, wherein the coating r comprises an emulsifier.

83. The use of any one of claims 1-82, wherein the ition further comprises one or more excipients, and the one or more excipients comprise a cellulose.

84. The use of any one of claims 1-83, wherein the medicament is released into the proximal small intestines following administration to the subject.

85. The use of any one of claims 1-83, wherein the medicament is released into the duodenum or jejunum portion of the small intestines following administration to the subject.

86. The use of any one of claims 1-83, wherein the medicament is ed into the ileum portion of the small intestines following administration to the subject.

87. The use of any one of claims 1-86, wherein the medicament is formulated for oral administration.

88. The use of any one of claims 1-86, wherein the medicament is formulated for administration directly into the gastrointestinal system.

89. The use of claim 88, wherein the ment is formulated for administration through a nasal-gastrointestinal tube (NG Tube) or a gastrointestinal tube (G-tube).

90. The use of any one of claims 1-89, wherein the subject exhibiting an ASD is between the ages of 1-18 years.

91. The use of any one of claims 1-89, n the subject exhibiting an ASD is between the ages of 2-16 years.

92. The use of any one of claims 1-89, wherein the subject exhibiting an ASD is between the ages of 1-10 years.

93. The use of any one of claims 1-89, wherein the subject ting an ASD is between the ages of 3-8 years.

94. The use of any one of claims 1-89, wherein the subject exhibiting an ASD is between the ages of 9-12 years.

95. The use of any one of claims 1-94, wherein the subject has an increase in vitamin intake (by weight) of Vitamin B6, n B12, n A, Vitamin C, Vitamin E, Vitamin K, Copper, Iron, Cholesterol, Niacin, Riboflavin, Thiamin, or Zinc in a blood sample or a fecal sample after stration of the medicament.

96. The use of any one of claims 1-94, wherein the subject has an increase in vitamin intake of one or more of plant-based Vitamin A, Carotenoids (alpha and beta carotene), Vitamin K, Vitamin E, Vitamin C, Selenium, copper, folate, lutein, lycopene, magnesium, potassium, orus, sodium, polyunsaturated fatty acids, monounsaturated fatty acids, ted fats, cholesterol, or Theobromine in a blood sample or a fecal sample following administration of the medicament.

97. The use of claim 95 or 96, wherein the increase in n intake by the subject after administration of the medicament is in comparison to before the subject began administration of the medicament.

98. The use of claim 95 or 96, wherein the increase in vitamin intake by the subject after administration of the medicament is in comparison to a subject administered a o.

99. The use of any one of claims 1-98, wherein the subject exhibiting an ASD further has a vitamin K deficiency.

100. The use of claim 99, wherein levels of gamma carboxylated proteins in the blood are indicative of the vitamin K deficiency.

101. The use of any one of claims 1-98, wherein a se in carboxylation of glutamate es is exhibited in the subject exhibiting an ASD.

102. The use of any one of claims 99-101, wherein the medicament is formulated for co-administration of vitamin K to the subject.

103. The use of any one of claims 1-102, n the subject exhibiting an ASD further exhibits an improvement in expressive language capabilities after administration of the medicament.

104. The use of any one of claims 1-103, wherein the subject exhibiting an ASD further exhibits an improvement in receptive language capabilities after administration of the medicament.

105. The use of claim 103 or 104, wherein the expressive language lities or receptive language capabilities are measured with an sive Vocabulary Test (EVT), a Peabody Picture lary Test (PPVT), or a combination thereof.

106. The use of claim 105, wherein the EVT test is an EVT-A test or an EVT-B test.

107. The use of claim 105, wherein the PPVT test is a PPVT-A test or a PPVT-B test.

108. The use of claim 105, wherein the subject administered the medicament has a greater improvement in expressive language capabilities than receptive ge capabilities.

109. The use of any one of claims 1-108, wherein the subject ting an ASD further exhibits an increase in body mass or physical growth after administration of the medicament.

110. The use of any one of claims 9, wherein the subject has been diagnosed as having the ASD before administration of the medicament.

111. The use of claim 110, wherein the subject has been diagnosed as having the ASD by a , a SCQ or a ADI-R .

112. The use of any one of claims 103-111, wherein the improvement is observed in the subject administered the medicament 12 weeks or more after the subject began administration of the medicament.

113. The use of claim 105, wherein the subject stered the medicament has a greater ement in an EVT score than a PPVT score.

114. The use of claim 105, wherein the subject administered the medicament has a greater improvement in an EVT score or a PPVT score after the subject began administration of the medicament.

115. The use of any one of claims 103-114, wherein the t has a more alkaline stool pH after administration of the medicament than prior to administration of the medicament.

116. The use of claim 115, wherein the t has more alkaline stool pH after at least four weeks of administration of the medicament than prior to administration of the medicament.

117. The use of any one of claims 103-114, wherein the subject has more alkaline stool pH after stration of the medicament than a subject administered a placebo.

118. The use of claim 117, wherein the subject has more alkaline stool pH after at least four weeks of administration of the medicament than a subject administered a placebo.

119. The use of any one of claims 103-114, wherein the subject has an abnormal fecal chymotrypsin level before administration of the medicament.

120. The use of claim 119, n the subject has a fecal chymotrypsin level of less than 13 U/g as measured in a frozen stool sample before administration of the medicament.

121. The use of claim 119, wherein the subject has a fecal chymotrypsin level of less than 12.6 U/g as ed in a frozen stool sample before administration of the medicament.

122. The use of claim 119, wherein the subject has a fecal chymotrypsin level of less than 10 U/g as measured in a fresh stool sample before administration of the medicament.

123. The use of claim 119, wherein the subject has a fecal chymotrypsin level of less than 9 U/g as measured in a fresh stool sample before administration of the medicament.

124. The use of any one of claims 3, wherein the subject has an increased fecal chymotrypsin level after administration of the medicament.

125. The use of claim 124, wherein the subject has an increased fecal chymotrypsin level after at least 12 weeks of administration of the medicament.

126. The use of claim 15, wherein the subject administered the medicament exhibits improvement in two, three, four, five, six, or more symptoms of the ASD.

127. The use of claim 1, wherein the subject further has one or more allergies and has a larger intake of fiber, calories, fat, and carbohydrates after administration of the ment than a subject that did not have allergies.

128. The use of the claim 1, wherein the ment is to be administered for at least 12 weeks.