WO2010132671A1 - Treatment of mci and alzheimer's disease - Google Patents

Treatment of mci and alzheimer's disease Download PDF

Info

Publication number
WO2010132671A1
WO2010132671A1 PCT/US2010/034721 US2010034721W WO2010132671A1 WO 2010132671 A1 WO2010132671 A1 WO 2010132671A1 US 2010034721 W US2010034721 W US 2010034721W WO 2010132671 A1 WO2010132671 A1 WO 2010132671A1
Authority
WO
WIPO (PCT)
Prior art keywords
nifedipine
effective amount
nitroso
therapeutically effective
pharmaceutical composition
Prior art date
Application number
PCT/US2010/034721
Other languages
French (fr)
Inventor
Mark Lovell
Bert Lynn
Original Assignee
The University Of Kentucky Research Foundation
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by The University Of Kentucky Research Foundation filed Critical The University Of Kentucky Research Foundation
Priority to CA2761298A priority Critical patent/CA2761298A1/en
Priority to AU2010249015A priority patent/AU2010249015A1/en
Priority to JP2012511013A priority patent/JP2012526844A/en
Priority to EP10775535A priority patent/EP2429992A4/en
Priority to MX2011012015A priority patent/MX2011012015A/en
Priority to PCT/US2010/057287 priority patent/WO2011142778A1/en
Priority to EP10851531.3A priority patent/EP2568811A4/en
Priority to JP2013510067A priority patent/JP2013526518A/en
Priority to CN2010800680043A priority patent/CN102984938A/en
Priority to AU2010353287A priority patent/AU2010353287A1/en
Priority to CA2799162A priority patent/CA2799162A1/en
Publication of WO2010132671A1 publication Critical patent/WO2010132671A1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/195Carboxylic acids, e.g. valproic acid having an amino group
    • A61K31/197Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
    • A61K31/198Alpha-amino acids, e.g. alanine or edetic acid [EDTA]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Definitions

  • AD Alzheimer's disease
  • MCI Mild Cognitive Impairment
  • Dr. Eschenbach stated that "the estimated 4.5 million cases of Alzheimer's today can be expected to rise to about 16 million by 2050.” Dr. Eschenbach explained that five drugs were approved for AD treatment — tacrine, rivastigmine, galantamine, donepezil, and memantine — the first four of which act by elevating acetylcholine levels in the brain, and the last of which is an antagonist of the N-methyl-D-aspartate receptor. Thus, Dr. Eschenbach pointed out that none of the five approved drugs have been shown to prevent or slow the underlying nerve degeneration in [AD] patients. He continued: "We await, together with the rest of the world, [] new drugs that may some day be able to treat the underlying cause of this insidious disease as well as other neurological diseases . . .”
  • the present invention encompasses the discovery that nifedipine and its oxidized or nitroso derivatives can effectively inhibit A ⁇ l-40 generation, reduce A ⁇ processing enzymes and inactivate related biochemical pathways, both in vitro and in vivo.
  • the present invention provides, among other things, novel therapeutic methods and compositions that can effectively treat, slow or prevent Mild Cognitive Impairment (MCI) and/or Alzheimer's disease, as well as delaying the progression from MCI to AD.
  • MCI Mild Cognitive Impairment
  • the present invention provides a pharmaceutical composition suitable for treating, slowing, or preventing Mild Cognitive Impairment (MCI) and/or Alzheimer's disease in a human subject comprising a therapeutically effective amount of one or more therapeutic agents and a pharmaceutically acceptable carrier.
  • a therapeutic agent is of formula (Ia) as defined and described herein.
  • a therapeutic agent is of formula (Ib) as defined and described herein.
  • a therapeutic agent suitable for the invention is selected from the group consisting of nifedipine, oxidized nifedipine, nitroso-nifedipine, thyroxine (T4), triiodothyronine (T3) and combinations thereof.
  • a therapeutic agent suitable for the invention is a calcium channel blocker. In some embodiments, a therapeutic agent suitable for the invention is not a calcium channel blocker.
  • a therapeutic agent suitable for the invention comprises nifedipine. In some embodiments, a therapeutic agent suitable for the invention comprises oxidized nifedipine. In some embodiments, a therapeutic agent suitable for the invention comprises nitroso-nifedipine. In some embodiments, a therapeutic agent suitable for the invention comprises a mixture of nitroso-nifedipine, oxidized nifedipine, and nifedipine. In some embodiments, a therapeutic agent suitable for the invention comprises 55% nitroso- nifedipine, 11% oxidized nifedipine, and 34% nifedipine.
  • various therapeutic agents described herein further comprises thyroxine (T4) and/or triiodothyronine (T3).
  • a therapeutic agent suitable for the invention comprises nifedipine, oxidized nifedipine, nitroso-nifedipine, thyroxine (T4) and/or triiodothyronine (T3).
  • a pharmaceutical composition according to the present invention comprises a therapeutic agent in a therapeutically effective amount of about 0.01 to about 1000 mg (e.g., about 0.01 to about 200 mg, about 0.01 to about 100 mg, about 0.1 to about 50 mg, about 0.01 to about 10 mg, about 0.01 to about 5 mg, about 0.01 to about 2.5 mg, about 0.01 to about 2.0 mg, about 0.01 to about 1.5 mg, about 0.01 to about 1.0 mg, about 0.01 to about 0.5 mg, about 0.01 to about 0.1 mg) per dose.
  • a therapeutic agent in a therapeutically effective amount of about 0.01 to about 1000 mg (e.g., about 0.01 to about 200 mg, about 0.01 to about 100 mg, about 0.1 to about 50 mg, about 0.01 to about 10 mg, about 0.01 to about 5 mg, about 0.01 to about 2.5 mg, about 0.01 to about 2.0 mg, about 0.01 to about 1.5 mg, about 0.01 to about 1.0 mg, about 0.01 to about 0.5 mg, about 0.01 to about 0.1 mg) per dose.
  • a pharmaceutical composition according to the present invention comprises nitroso-nifedipine in a therapeutically effective amount of about 10 mg to 2.5 g (e.g., about 10 mg to 2.0 g, about 10 mg to 1.5 g, about 10 to about 1000 mg, about 10 mg to about 500 mg) per dose.
  • a pharmaceutical composition according to the present invention is formulated for oral, subcutaneous, intravenous, transdermal, intraperitoneal, intramuscular, intracerebroventricular, intraparenchymal, intrathecal, intracranial, buccal, mucosal, nasal, or rectal administration.
  • a pharmaceutical composition according to the present invention is formulated for oral administration.
  • a pharmaceutical composition according to the invention is formulated for immediate or extended release.
  • the present invention provides a method for treating, slowing, or preventing Mild Cognitive Impairment (MCI) and/or Alzheimer's disease in a human subject, the method comprising administering to a subject who is suffering from or susceptible to MCI or Alzheimer's disease a therapeutically effective amount of one or more therapeutic agents, such that at least one symptom or feature associated with the MCI or Alzheimer's disease is reduced in abundance, intensity, severity, or frequency, or has delayed onset.
  • MCI Mild Cognitive Impairment
  • a symptom or feature is cognitive decline, production of amyloid beta protein, beta-secretase activity, gamma-secretase activity, paired helical filaments, phosphorylated tau protein in the brain, and/or an immune or inflammatory condition in the central nervous system.
  • the gamma-secretase activity is reduced by inhibiting presenilin-1 (PS-I), nicastrin, APH-I and/or PEN-2 activity.
  • the gamma-secretase activity is reduced by inhibiting orphan G-coupled receptor 3 (GPCR-3) activity.
  • an immune or inflammatory condition is reduced by decreasing the level of one or more cytokines (e.g., IL-I, IL-6, TNF- ⁇ ) in the central nervous system.
  • cytokines e.g., IL-I, IL-6, TNF- ⁇
  • a therapeutic agent used in a method according to the present invention is of formula (Ia) as defined and described herein.
  • a therapeutic agent used in a method according to the invention is of formula (Ib) as defined and described herein.
  • a suitable therapeutic agent is selected from the group consisting of nifedipine, oxidized nifedipine, nitroso-nifedipine, thyroxine (T4), triiodothyronine (T3) and combinations thereof.
  • a suitable therapeutic agent is a calcium channel blocker. In some embodiments, a suitable therapeutic agent is not a calcium channel blocker.
  • a suitable therapeutic agent comprises nifedipine. In some embodiments, a suitable therapeutic agent comprises oxidized nifedipine. In some embodiments, a suitable therapeutic agent comprises nitroso-nifedipine. In some embodiments, a suitable therapeutic agent used in a method according to the present invention comprises a mixture of nitroso-nifedipine, oxidized nifedipine, and nifedipine. In some embodiments, a suitable therapeutic agent used in a method according to the present invention comprises 55% nitroso- nifedipine, 11% oxidized nifedipine, and 34% nifedipine. In some embodiments, suitable agents described herein further comprises T3/T4.
  • an suitable agent used in a method of the present invention comprising nifedipine, oxidized nifedipine, and/or nitroso- nifedipine further comprises thyroxine (T4) and/or triiodothyronine (T3).
  • a method according to the present invention administers to a subject in need of treatment a therapeutic agent in a therapeutically effective amount of about 0.01 to about 1000 mg (e.g., about 0.01 to about 200 mg, about 0.01 to about 100 mg, about 0.1 to about 50 mg, about 0.01 to about 10 mg, about 0.01 to about 5 mg, about 0.01 to about 2.5 mg, about 0.01 to about 2.0 mg, about 0.01 to about 1.5 mg, about 0.01 to about 1.0 mg, about 0.01 to about 0.5 mg, about 0.01 to about 0.1 mg) per dose.
  • a therapeutic agent in a therapeutically effective amount of about 0.01 to about 1000 mg (e.g., about 0.01 to about 200 mg, about 0.01 to about 100 mg, about 0.1 to about 50 mg, about 0.01 to about 10 mg, about 0.01 to about 5 mg, about 0.01 to about 2.5 mg, about 0.01 to about 2.0 mg, about 0.01 to about 1.5 mg, about 0.01 to about 1.0 mg, about 0.01 to about 0.5 mg, about 0.01 to about 0.1 mg
  • a method according to the present invention administers to a subject in need of treatment a therapeutic agent comprising nitroso-nifedipine in a therapeutically effective amount of about 10 mg to about 2.5 g (e.g., about 10 mg to about 2.0 g, about 10 mg to about 1.5 g, about 10 mg to about 1000 mg, or about 10 mg to about 500 mg) per dose.
  • an agent used in a method according to the present invention is administered by oral, subcutaneous, intravenous, transdermal, intraperitoneal, intramuscular, intracerebroventricular, intraparenchymal, intrathecal, intracranial, buccal, mucosal, nasal, or rectal administration.
  • an agent used in a method according to the present invention is administered orally.
  • an agent is administered monthly, bi-weekly, or weekly. In some embodiments, according to a method of the present invention, an agent is administered daily. In some embodiments, according to a method of the present invention, an agent is administered twice daily, three times daily, or four times daily.
  • a subject treated by a method of the present invention has a diminished or elevated level of a biomarker (e.g., a protein biomarker complex) as compared to a control.
  • a suitable biomarker is a protein biomarker complex comprising at least one of a transthyretin protein and/or a prostaglandin-H2 D-isomerase protein, and at least one second, different protein selected from a transthyretin, prostaglandin-H2 D- isomerase, beta-2-microglobulin, cystatin C, superoxide dismutase [Cu-Zn], plasma retinol- binding protein, phosphatidylethanolamine -binding protein, carbonic anhydrase 2, and/or serotransferrin protein.
  • a suitable protein biomarker complex comprises prostaglandin-D2-synthase and transthyretin (PDS/TTR complex).
  • a suitable biomarker comprises one or more of (i) beta amyloid 40 (A ⁇ 40), (ii) beta amyloid 42 (A ⁇ 42), (iii) the ratio of A ⁇ 40 to A ⁇ 42, and (iv) the ratio of phosphorylated tau to total tau.
  • a biomarker is determined in a fluid sample (e.g., CSF, serum, whole blood, blood plasma, urine, ascitic fluid, saliva, tissue effusion, lavage, and combinations thereof) obtained from the subject.
  • a suitable control is indicative of a level of the biomarker in a subject selected from the group consisting of a healthy individual, a patient suffering from Alzheimer's disease with a pre-determined stage, the subject before the treatment, and combinations thereof.
  • a subject to be treated has a test score indicative of cognitive impairment.
  • a test score indicative of cognitive impairment is an MMSE score (e.g., lower than 27, e.g., 21-26).
  • a test score indicative of cognitive impairment is a CDR score (e.g., above 0, e.g., 0.5, e.g., 1).
  • a method according to the invention further includes a step of first determining the therapeutically effective amount of the therapeutic agent based on the level of a biomarker and/or a cognitive test score.
  • the invention provides a solid oral dosage form comprising nitroso-nifedipine and nifedipine, and wherein the mass ratio of nitroso-nifedipine to nifedipine is at least about 1 :1 (e.g., at least about 2:1, at least about 4:1, at least about 8:1, at least about 16:1, at least about 32:1, at least about 64:1, at least about 100:1, at least about 200:1, at least about 500:1, or at least about 1000:1).
  • the mass ratio of nitroso-nifedipine to nifedipine is at least about 1 :1 (e.g., at least about 2:1, at least about 4:1, at least about 8:1, at least about 16:1, at least about 32:1, at least about 64:1, at least about 100:1, at least about 200:1, at least about 500:1, or at least about 1000:1).
  • a solid oral dosage form according to the present invention further comprises one or more pharmaceutically acceptable excipients (e.g., a binder, a buffer, a diluent, a dispersant, an emollient, a film-forming agent, a glidant, a light-blocking agent, a preservative, a solvent, a stabilizing agent, a surfactant, a suspending agent, and/or a tonicity agent).
  • a solid dosage form is for controlled or extended release.
  • a solid dosage form is for immediate release.
  • Figure 1 illustrates an exemplary Western blot analysis of the PDS/TTR complex expressed in cell culture medium by control epithelial cells, control epithelial cells treated with acrolein, and late stage AD epithelial cells.
  • Figure 2 illustrates exemplary survival data for cortical neurons treated with medium from control epithelial cells or AD epithelial cells.
  • Figure 3 illustrates exemplary results indicating that PHFl immunopositivity was detected in SY5Y cells resulting from exposure to the PDS/TTR protein complex.
  • Figure 4 illustrates exemplary Western blot data showing reduction of the
  • Figure 5 summarizes the numbers of PDS/TTR-positive cells determined by immunostaining in cultures treated with acrolein, acrolein plus T3/T4, acrolein plus nifedipine mixture (nitroso nifedipine 55%, oxidized nifedipine 11% and nifedipine 34%) and acrolein plus nifedipine mix and T3/T4.
  • Figure 6 illustrates that nifedipine mix does not function as a calcium channel blocker compared to fresh nifedipine as determined by confocal microscopy and a calcium fluorescent dye.
  • Figure 7 illustrates exemplary results indicating that inflammatory cytokine production was inhibited by nifedipine mix.
  • Figure 8 illustrates quantification of PHF-I immunostaining for SY5Y cultures treated with medium from epithelial cells treated with acrolein and combinations of nifedipine, analogs, mixtures and T3/T4.
  • Figure 9 illustrates exemplary results indicating that ABi_42 generation is inhibited by nifedipine, oxidized nifedipine, nitroso nifedipine and T3/T4.
  • Figure 10 illustrates exemplary results indicating effect of nifedipine, nifedipine analogs and nifedipine mix, with and without T3/T4 on A ⁇ i_4 2 production from H4 cells.
  • Figure 11 illustrates exemplary results indicating effects of known calcium channel blockers such as Amilodpine, Dilitiazem, Felodipine, Isradipine, Nicardipine, and Nimodipine on A ⁇ 1-42 generation in H4 neuroglioma cultures.
  • known calcium channel blockers such as Amilodpine, Dilitiazem, Felodipine, Isradipine, Nicardipine, and Nimodipine on A ⁇ 1-42 generation in H4 neuroglioma cultures.
  • Figure 12 illustrates exemplary results indicating that nitroso-nifedipine significantly inhibits BACE activity.
  • Figure 13 illustrates exemplary results indicating the effect of nifedipine mix on
  • Figure 14 illustrates exemplary results indicating the effect of nifedipine, nifedipine mix and/or T3/T4 on AB 1-40 generation and certain AB 1-40 processing enzymes in a mouse model.
  • Figure 15 illustrates exemplary results indicating that nifedipine, nifedipine mix and/or T3/T4 reduced GPCR-3 levels in H4 cultures or in mice treated acutely with drugs.
  • the GPCR-3 levels were determined using Western blot analysis.
  • Figure 15a illustrates exemplary results indicating the effect of other classes of blood pressure drugs on the levels of GPCR-3 in H4 cultures with and without T3/T4.
  • Figure 16 illustrates exemplary results indicating the effect of nifedipine, nifedipine mix and/or T3/T4 on the levels of enzymes involved in Tau phosphorylation measured in the mouse brains treated with corresponding compounds.
  • Figure 17 illustrates exemplary trajectories fitted according to the NLMIXED model of MMSE verse age based on a human association study.
  • Figure 18 illustrates exemplary results indicating levels of A ⁇ 1-42 and A ⁇ processing enzymes such as PS-I, Nicas, BACE, APH-I and PEN-2 in front lobe specimens of subjects from a neuropsychological test score association study who came to autopsy. 4 subjects were on calcium channel blockers, including nifedipine and 4 subjects were not on any calcium channel blocker. AB levels determined using Invitrogen ELISAs. Protein levels determined using Western blot analysis and antibodies specific to each protein.
  • Figure 19 illustrates exemplary results indicating enzyme levels involved in Tau phosphorylation in frontal lobe specimens from the same subjects shown in Figure 18.
  • Figure 20 illustrates exemplary results from a photochemical synthesis of nitroso- nifedipine.
  • Alzheimer's patient As used herein, the terms “Alzheimer's patient,” “AD patient,” and “individual diagnosed with AD” all refer to an individual who has been diagnosed with AD or has been given a probable diagnosis of Alzheimer's Disease (AD).
  • Animal As used herein, the term “animal” refers to any member of the animal kingdom. In some embodiments, “animal” refers to humans, at any stage of development. In some embodiments, “animal” refers to non-human animals, at any stage of development.
  • the non-human animal is a mammal (e.g., a rodent, a mouse, a rat, a rabbit, a monkey, a dog, a cat, a sheep, cattle, a primate, and/or a pig).
  • animals include, but are not limited to, mammals, birds, reptiles, amphibians, fish, insects, and/or worms.
  • an animal may be a transgenic animal, genetically-engineered animal, and/or a clone.
  • Bio fluid sample encompasses a variety of fluid sample types obtained from an individual and can be used in a diagnostic or monitoring assay.
  • the term encompasses whole blood, blood serum or blood plasma, cerebrospinal fluid (CSF), urine and other liquid samples of biological origin.
  • CSF cerebrospinal fluid
  • the term also includes samples that have been manipulated in any way after their procurement, such as by treatment with reagents, solubilization, or enrichment for certain components, such as proteins or polynucleotides.
  • Combination therapy refers to those situations in which two or more different pharmaceutical agents are administered in overlapping regimens so that the subject is simultaneously exposed to both agents.
  • Control has its art-understood meaning of being a standard against which results are compared. Typically, controls are used to augment integrity in experiments by isolating variables in order to make a conclusion about such variables.
  • a control is a reaction or assay that is performed simultaneously with a test reaction or assay to provide a comparator. In one experiment, the "test” (i.e., the variable being tested) is applied. In the second experiment, the "control,” the variable being tested is not applied.
  • a control is a historical control (i.e., of a test or assay performed previously, or an amount or result that is previously known).
  • a control is or comprises a printed or otherwise saved record. A control may be a positive control or a negative control.
  • Dosing regimen refers to a set of unit doses (at least one and often more than one) that are administered individually separated by periods of time.
  • the recommended set of doses i.e., amounts, timing, route of administration, etc.
  • a particular therapeutic agent constitutes its dosing regimen.
  • a "functional" biological molecule is a biological molecule in a form in which it exhibits a property and/or activity by which it is characterized.
  • inhibiting a protein or a gene refers to processes or methods of decreasing or reducing activity and/or expression of a protein or a gene of interest.
  • inhibiting a protein or a gene refers to reducing expression or a relevant activity of the protein or gene by at least 10% or more, for example, 20%, 30%, 40%, or 50%, 60%, 70%, 80%, 90% or more, or a decrease in expression or the relevant activity of greater than 1-fold, 2-fold, 3-fold, 4-fold, 5-fold, 10-fold, 50-fold, 100-fold or more as measured by one or more methods described herein or recognized in the art.
  • in vitro refers to events that occur in an artificial environment, e.g., in a test tube or reaction vessel, in cell culture, etc., rather than within a multi-cellular organism.
  • in vivo refers to events that occur within a multi-cellular organism such as a non-human animal.
  • Isolated refers to a substance and/or entity that has been (1) separated from at least some of the components with which it was associated when initially produced (whether in nature and/or in an experimental setting), and/or (2) produced, prepared, and/or manufactured by the hand of man. Isolated substances and/or entities may be separated from at least about 10%, about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, about 90%, about 95%, about 98%, about 99%, substantially 100%, or 100% of the other components with which they were initially associated.
  • isolated agents are more than about 80%, about 85%, about 90%, about 91%, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, about 99%, substantially 100%, or 100% pure.
  • a substance is "pure” if it is substantially free of other components.
  • isolated cell refers to a cell not contained in a multi-cellular organism.
  • an individual with MCI is typically an individual who meets the following clinical criteria of amnestic MCI (Petersen et al. Arch Neural 56:303-308 (1999): 1) memory complaints corroborated by an informant, 2) objective memory impairment for age and education, 3) normal general cognitive function, 4) intact activities of daily living, and 5) the subject does not meet criteria for dementia.
  • an "individual with EAD (early or moderate Alzheimer's disease)” is an individual who demonstrate the following criteria: 1) a decline in cognitive function for a previous higher level, 2) declines in one or more areas of cognition in addition to memory, 3) a clinical dementia rating scale score of 0.5 to 1, and 4) a clinical examination that excluded other causes of dementia.
  • an "individual with LAD (severe or late stage Alzheimer's disease)" is an individual who meets the standard clinical diagnostic criteria for probable AD (McKhann et al. Neurology 34:939-48 (1984).
  • Reference value can be an absolute value; a relative value; a value that has an upper and/or lower limit; a range of values; an average value; a median value, a mean value, or a value as compared to a particular control or baseline value.
  • a reference value can be based on an individual sample value, such as for example, a value obtained from a sample from the individual with AD, MCI or cognitive impairment, but at an earlier point in time, or a value obtained from a sample from an AD patient other than the individual being tested, or a "normal" individual, that is an individual not diagnosed with AD.
  • the reference value can be based on a large number of samples, such as from AD patients or normal individuals or based on a pool of samples including or excluding the sample to be tested.
  • Neurological disease refers to a disease or disorder of the central nervous system. Neurological diseases include multiple sclerosis, neuropathies, and neurodegenerative disorders such as AD, Parkinson's disease, amyotrophic lateral sclerosis (ALS), mild cognitive impairment (MCI) and frontotemporal dementia.
  • AD Alzheimer's disease
  • ALS amyotrophic lateral sclerosis
  • MCI mild cognitive impairment
  • Normal individual As used herein, a "Normal" individual or “healthy” individual refers to an individual who has or would be assessed by a physician as not having AD or MCI, and has an Mini-Mental State Examination (MMSE) (referenced in Folstein et al., J. Psychiatr. Res 1975; 12:1289-198) score or would achieve a MMSE score in the range of 25-30.
  • MMSE Mini-Mental State Examination
  • a “Normal” individual is generally age-matched within a range of 5 to 10 years, including but not limited to an individual that is age-matched, with the individual to be assessed.
  • Protein refers to a polypeptide ⁇ i.e., a string of at least two amino acids linked to one another by peptide bonds). Proteins may include moieties other than amino acids ⁇ e.g., may be glycoproteins, proteoglycans, etc.) and/or may be otherwise processed or modified. Those of ordinary skill in the art will appreciate that a “protein” can be a complete polypeptide chain as produced by a cell (with or without a signal sequence), or can be a characteristic portion thereof. Those of ordinary skill will appreciate that a protein can sometimes include more than one polypeptide chain, for example linked by one or more disulfide bonds or associated by other means.
  • Polypeptides may contain L-amino acids, D- amino acids, or both and may contain any of a variety of amino acid modifications or analogs known in the art. Useful modifications include, e.g., terminal acetylation, amidation, etc.
  • proteins may comprise natural amino acids, non-natural amino acids, synthetic amino acids, and combinations thereof.
  • the term "peptide” is generally used to refer to a polypeptide having a length of less than about 100 amino acids.
  • Subject refers to any organism to which compositions in accordance with the invention may be administered, e.g. , for experimental, diagnostic, prophylactic, and/or therapeutic purposes. Typical subjects include animals (e.g., mammals such as mice, rats, rabbits, non-human primates, and humans; insects; worms; etc.).
  • the term “substantially” refers to the qualitative condition of exhibiting total or near-total extent or degree of a characteristic or property of interest.
  • One of ordinary skill in the biological arts will understand that biological and chemical phenomena rarely, if ever, go to completion and/or proceed to completeness or achieve or avoid an absolute result.
  • the term “substantially” is therefore used herein to capture the potential lack of completeness inherent in many biological and chemical phenomena.
  • Susceptible to An individual who is "susceptible to" a disease, disorder, and/or condition has not been diagnosed with the disease, disorder, and/or condition. In some embodiments, an individual who is susceptible to a disease, disorder, and/or condition may not exhibit symptoms of the disease, disorder, and/or condition. In some embodiments, an individual who is susceptible to a disease, disorder, and/or condition will develop the disease, disorder, and/or condition. In some embodiments, an individual who is susceptible to a disease, disorder, and/or condition will not develop the disease, disorder, and/or condition.
  • therapeutically effective amount As used herein, the term "therapeutically effective amount" of a therapeutic agent means an amount that is sufficient, when administered to a subject suffering from or susceptible to a disease, disorder, and/or condition, to treat, diagnose, prevent, and/or delay the onset of the symptom(s) of the disease, disorder, and/or condition.
  • therapeutic agent refers to any agent that, when administered to a subject, has a therapeutic effect and/or elicits a desired biological and/or pharmacological effect.
  • therapeutic agent and “agent” are used inter-changeably.
  • Treating refers to any method used to partially or completely alleviate, ameliorate, relieve, inhibit, prevent, delay onset of, reduce severity of and/or reduce incidence of one or more symptoms or features of a particular disease, disorder, and/or condition. Treatment may be administered to a subject who does not exhibit signs of a disease and/or exhibits only early signs of the disease for the purpose of decreasing the risk of developing pathology associated with the disease.
  • the compounds of the present invention may exist in particular geometric or stereoisomeric forms.
  • the present invention contemplates all such compounds, including cis- and trans-isomers, R- and S-enantiomers, diastereomers, (D)-isomers, (L)-isomers, the racemic mixtures thereof, and other mixtures thereof, as falling within the scope of the invention.
  • Aliphatic denotes a hydrocarbon moiety that may be straight-chain (i.e., unbranched), branched, or cycloaliphatic (including fused, bridging, and spiro-fused polycyclic) and may be completely saturated or may contain one or more units of unsaturation, but which is not aromatic. Unless otherwise specified, aliphatic groups contain 1-6 carbon atoms. In some embodiments, aliphatic groups contain 1-4 carbon atoms, and in yet other embodiments aliphatic groups contain 1-3 carbon atoms.
  • Suitable aliphatic groups include, but are not limited to, linear or branched, alkyl, alkenyl, and alkynyl groups, and hybrids thereof such as (cycloalkyl)alkyl, (cycloalkenyl)alkyl or (cycloalkyl)alkenyl.
  • Alkenyl denotes a monovalent group derived from a straight- or branched-chain aliphatic moiety having at least one carbon-carbon double bond by the removal of a single hydrogen atom. In certain embodiments, alkenyl contains 2-6 carbon atoms. In certain embodiments, alkenyl contains 2-5 carbon atoms. In some embodiments, alkenyl contains 2-4 carbon atoms. In another embodiment, alkenyl contains 2-3 carbon atoms. Alkenyl groups include, for example, ethenyl ("vinyl”), propenyl ("allyl”), butenyl, l-methyl-2-buten-l-yl, and the like.
  • Alkyl refers to a monovalent saturated, straight- or branched-chain hydrocarbon radical derived from an aliphatic moiety containing between one and six carbon atoms by removal of a single hydrogen atom. In some embodiments, alkyl contains 1-5 carbon atoms. In another embodiment, alkyl contains 1-4 carbon atoms. In still other embodiments, alkyl contains 1-3 carbon atoms. In yet another embodiment, alkyl contains 1-2 carbons.
  • alkyl radicals include, but are not limited to, methyl, ethyl, n-propyl, isopropyl, n-butyl, iso-butyl, sec-butyl, sec-pentyl, iso-pentyl, tert- butyl, n-pentyl, neopentyl, n-hexyl, sec-hexyl, n-heptyl, n-octyl, n-decyl, n-undecyl, dodecyl, and the like.
  • Alkynyl refers to a monovalent group derived from a straight- or branched-chain aliphatic moiety having at least one carbon-carbon triple bond by the removal of a single hydrogen atom. In certain embodiments, alkynyl contains 2-6 carbon atoms. In certain embodiments, alkynyl contains 2-5 carbon atoms. In some embodiments, alkynyl contains 2-4 carbon atoms. In another embodiment, alkynyl contains 2-3 carbon atoms. Representative alkynyl groups include, but are not limited to, ethynyl, 2-propynyl ("propargyl”), 1-propynyl, and the like.
  • amino refers to a group of the formula (-
  • Alkoxy refers to a "substituted hydroxyl" of the formula (-
  • R 1 is an alkyl group, as defined herein, and the oxygen moiety is directly attached to the parent molecule.
  • alkylamino refers to a "substituted amino" of the formula (-NR h 2), wherein R h is, independently, a hydrogen or an alkyl group, as defined herein, and the nitrogen moiety is directly attached to the parent molecule.
  • Cycloaliphatic The terms “cycloaliphatic”, “carbocycle”, “carbocyclyl”,
  • Carbocyclo or “carbocyclic”, used alone or as part of a larger moiety, refer to a saturated or partially unsaturated cyclic aliphatic monocyclic or bicyclic ring systems, as described herein, having from 3 to 10 members, wherein the aliphatic ring system is optionally substituted as defined above and described herein.
  • Cycloaliphatic groups include, without limitation, cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cycloheptyl, cycloheptenyl, cyclooctyl, cyclooctenyl, and cyclooctadienyl.
  • the cycloalkyl has 3-6 carbons.
  • cycloaliphatic also include aliphatic rings that are fused to one or more aromatic or nonaromatic rings, such as decahydronaphthyl, tetrahydronaphthyl, decalin, or bicyclo[2.2.2]octane, where the radical or point of attachment is on an aliphatic ring.
  • Cyano refers to a group of the formula (-CN).
  • Halogen refers to an atom selected from fluorine (fluoro, -F), chlorine (chloro, -Cl), bromine (bromo, -Br), and iodine (iodo, -I).
  • Nitro refers to a group of the formula (-NO 2 ).
  • Nitroso refers to a group of the formula (-
  • Partially unsaturated refers to a ring moiety that includes at least one double or triple bond between ring atoms but is not aromatic.
  • the term “partially unsaturated” is intended to encompass rings having multiple sites of unsaturation, but is not intended to include aryl or heteroaryl moieties, as herein defined.
  • Unsaturated means that a moiety has one or more units of unsaturation.
  • the present invention provides, among other things, therapeutic compositions and methods that can effectively treat, slow or prevent mild cognitive impairment (MCI) or Alzheimer's disease (AD).
  • MCI mild cognitive impairment
  • AD Alzheimer's disease
  • the present invention is, in part, based on the following unexpected discoveries: (1) a protein complex PDS/TTR, known as a biomarker for early diagnosis of MCI or Alzheimer's disease, is neurotoxic and induces characteristic symptoms and features of Alzheimer's disease in cell cultures; (2) dihydropyridine calcium channel blockers (like nifedipine), their oxidized, nitroso derivatives and mixtures (which no longer function as calcium channel blockers), and/or T3/T4 effectively reduce or eliminate the ability of the PDS/TTR complex to induce AD-like symptoms and underlying enzymes and biochemical pathways in cell cultures and reduce endogenous levels of A ⁇ 1-40 peptide in animal models; and (3) human association studies demonstrated that the use of dihydropyridine calcium channel blockers significantly delays the onset of cognitive decline thus indicating that these compounds may be used to effectively treat Alzheimer's disease.
  • oxidized, nitroso nifedipine derivatives and mixtures no longer function as calcium channel blockers.
  • the ability of these compounds to treat MCI or Alzheimer's disease may be independent of their ability to block calcium channels.
  • the present invention contemplates methods and compositions that can effectively treat Alzheimer's disease based on therapeutically effective amount of nifedipine, oxidized or nitroso nifedipine derivatives, thyroxine (T4), triiodothyronine (T3) and combinations thereof.
  • the present invention provides methods for treating, slowing, or preventing Mild Cognitive Impairment (MCI) and/or Alzheimer's disease in a human subject, comprising administering to a subject who is suffering from or susceptible to MCI or Alzheimer's disease a therapeutically effective amount of an agent selected from the group consisting of nifedipine, oxidized nifedipine, nitroso-nifedipine, thyroxine (T4), triiodothyronine (T3) and combinations thereof, such that at least one symptom or feature associated with the MCI or Alzheimer's disease is reduced in abundance, intensity, severity, or frequency, or has delayed onset.
  • the agent suitable for the invention does not function as a calcium channel blocker.
  • inventive methods according to the invention can be combined with sensitive biomarkers and/or cognitive test scores to identify patents, including those at an early stage of the disease, for treatment and to monitor efficacy of the treatment.
  • the present invention is particularly useful to treat early stage patients, especially, those patients having symptoms described as Mild Cognitive Impairment (MCI) and/or to prevent progression of MCI to Alzheimer's disease.
  • MCI Mild Cognitive Impairment
  • Therapeutic agents suitable for the present invention include both calcium channel blockers (e.g., dihydropyridine calcium channel blockers such as nifedipine) and non-calcium channel blockers (e.g., oxidized nifedipine, nitroso-nifedipine, mixture of nifedipine and its derivatives, thyroxine (T4), triiodothyronine (T3)).
  • calcium channel blockers e.g., dihydropyridine calcium channel blockers such as nifedipine
  • non-calcium channel blockers e.g., oxidized nifedipine, nitroso-nifedipine, mixture of nifedipine and its derivatives, thyroxine (T4), triiodothyronine (T3).
  • a therapeutic agent suitable for the present invention is of formula (Ia) or (Ib):
  • R 5 is halogen, Ci_6 aliphatic, hydroxyl, alkoxy, amino, alkylamino, cyano, nitro, or nitroso; and n is 0, 1, 2, or 3.
  • R 1 and R 2 are independently Ci_ 3 alkyl. In some embodiments, R 3 and R 4 are independently Ci_4 alkyl. In some embodiments, R 1 and R 2 are methyl. In some embodiments, R 3 and R 4 are methyl.
  • a therapeutic agent suitable for the present invention is nifedipine, oxidized nifedipine, or nitroso-nifedipine.
  • nitroso-nifedipine is an oxidized analog of nifedipine, as shown below.
  • therapeutic agents suitable for the present invention include, but are not limited to, dihyropyridine compounds such as amlodipine, aranidipine, azelnidipine, barnidipine, benidipine, cilnidipine, clevidipine, efonidipine, felodipine, isradipine, lacidipine, manidipine, lercanidipine, nicardipine, nifedipine, nilvadipine, nimodipine, nisoldipine, nitrendipine, and pranidipine.
  • dihyropyridine compounds such as amlodipine, aranidipine, azelnidipine, barnidipine, benidipine, cilnidipine, clevidipine, efonidipine, felodipine, isradipine, lacidipine, manidipine, lercanidipine, nicardipine,
  • therapeutic agents suitable for the present invention include, but are not limited to, oxidized amlodipine, oxidized aranidipine, oxidized azelnidipine, oxidized barnidipine, oxidized benidipine, oxidized cilnidipine, oxidized clevidipine, oxidized efonidipine, oxidized felodipine, oxidized isradipine, oxidized lacidipine, oxidized manidipine, oxidized lercanidipine, oxidized nicardipine, oxidized nifedipine, oxidized nilvadipine, oxidized nimodipine, oxidized nisoldipine, oxidized nitrendipine, and oxidized pranidipine.
  • an "oxidized" dihydropyridine compound e.g., oxidized amlodipine, oxidized nimodipine, oxidized nivaldipine
  • oxidized amlodipine, oxidized nimodipine, oxidized nivaldipine is the pyridine version of said compound.
  • exemplary therapeutic agents include the following:
  • a therapeutic agent suitable for the present invention is of formula (II):
  • X is -CH 2 -. In some embodiments, X is -O-. In some embodiments, X is -NH-.
  • a therapeutic agent suitable for the present invention is thyroxine (T4) or triiodothyronine (T3):
  • T3 triiodothyronine
  • T4 thyroxine
  • a therapeutic agent suitable for the present invention is a mixture of various compounds described herein.
  • two or more compounds of formula (Ia) or (Ib) can be combined to form a therapeutic agent.
  • two or more of nifedipine, oxidized nifedipine, and nitroso-nifedipine are combined.
  • T3 and/or T4 are combined with one or more of nifedipine, oxidized nifedipine, and nitroso-nifedipine.
  • nifedipine, oxidized nifedipine, and nitroso- nifedipine are combined to form a nifedipine mix or mixture.
  • a therapeutic agent according to the invention can be a mixture of two or more of nifedipine, oxidized nifedipine, nitroso-nifedipine, thyroxine (T4), and triiodothyronine (T3) at predetermined mass or molar ratios.
  • a therapeutic agent suitable for the invention contains a mixture of nitroso-nifedipine and nifedipine.
  • nitroso-nifedipine and nifedipine can be mixed at a mass or molar ratio of about 1000:1, about 500:1, about 200:1, about 100:1, about 64:1, about 32:1, about 16:1, about 10:1, about 8:1, about 5:1, about 4:1, about 3:1, about 2:1, about 1 :1, about 1 :2, about 1 :3, about 1 :4, about 1 :5, about 1 :8, about 1 :10, about 1 :16, about 1 :32, about 1 :64, about 1 :100, about 1 :200, about 1 :500, or about 1 : 1000.
  • nitroso-nefidipine and nifedipine can be mixed at a mass or molar ratio ranging from about 1 :1000 to about 1000:1 (e.g., about 1 :500 to about 500:1, about 1 :200 to about 200:1, about 1 : 100 to about 100:1, about 1 : 10 to about 10:1, about 1 : 16 to about 16:1, about 1:32 to about 32:1, about 1:64 to about 64:1, about 1:1 to about 32:1, about 1:1 to about 10:1, about 100:1 to about 1000:1, about 10:1 to about 100:1, about 1:1000 to 1:1, about 1:1 to about 1000:1, or about 1:100 to about 1:10).
  • about 1 :1000 to about 1000:1 e.g., about 1 :500 to about 500:1, about 1 :200 to about 200:1, about 1 : 100 to about 100:1, about 1 : 10 to about 10:1, about 1 : 16 to about 16:1, about 1:32 to about 32:1, about 1:64 to
  • a therapeutic agent suitable for the invention contains a mixture of oxidized-nifedipine and nifedipine.
  • oxidized-nifedipine and nifedipine can be mixed at a mass or molar ratio of about 1000:1, about 500:1, about 200:1, about 100:1, about 64:1, about 32:1, about 16:1, about 10:1, about 8:1, about 5:1, about 4:1, about 3:1, about 2:1, about 1:1, about 1:2, about 1:3, about 1:4, about 1:5, about 1:8, about 1:10, about 1:16, about 1:32, about 1:64, about 1:100, about 1:200, about 1 :500, or about 1 : 1000.
  • oxidized-nefidipine and nifedipine can be mixed at amass or molar ratio ranging from about 1:1000 to about 1000:1 (e.g., about 1:500 to about 500:1, about 1:200 to about 200:1, about 1:100 to about 100:1, about 1:10 to about 10:1, about 1:16 to about 16:1, about 1:32 to about 32:1, about 1:64 to about 64:1, about 1:1 to about 32:1, about 1:1 to about 10:1, about 100:1 to about 1000:1, about 10:1 to about 100:1, about 1:1000 to 1:1, about 1:1 to about 1000:1, or about 1:100 to about 1:10).
  • about 1:1000 to about 1000:1 e.g., about 1:500 to about 500:1, about 1:200 to about 200:1, about 1:100 to about 100:1, about 1:10 to about 10:1, about 1:16 to about 16:1, about 1:32 to about 32:1, about 1:64 to about 64:1, about 1:1 to about 32:1, about 1:1 to about 10:1, about 100
  • a therapeutic agent suitable for the invention contains a mixture of nitroso-nifedipine and oxidized nifedipine.
  • nitroso-nifedipine and oxidized-nifedipine can be mixed at a mass or molar ratio of about 1000:1, about 500:1, about 200:1, about 100:1, about 64:1, about 32:1, about 16:1, about 10:1, about 8:1, about 5:1, about 4:1, about 3:1, about 2:1, about 1:1, about 1:2, about 1:3, about 1:4, about 1:5, about 1:8, about 1:10, about 1:16, about 1:32, about 1:64, about 1:100, about 1:200, about 1:500, or about 1:1000.
  • nitroso- nefidipine and oxidized nifedipine can be mixed at a mass or molar ratio ranging from about 1:1000 to about 1000:1 (e.g., about 1:500 to about 500:1, about 1:200 to about 200:1, about 1:100 to about 100:1, about 1:10 to about 10:1, about 1:16 to about 16:1, about 1:32 to about 32:1, about 1:64 to about 64:1, about 1:1 to about 32:1, about 1:1 to about 10:1, about 100:1 to about 1000:1, about 10:1 to about 100:1, about 1:1000 to 1:1, about 1:1 to about 1000:1, or about 1 : 100 to about 1:10).
  • about 1:1000 to about 1000:1 e.g., about 1:500 to about 500:1, about 1:200 to about 200:1, about 1:100 to about 100:1, about 1:10 to about 10:1, about 1:16 to about 16:1, about 1:32 to about 32:1, about 1:64 to about 64:1, about 1:1 to about 32:1, about 1:1 to
  • a therapeutic agent suitable for the invention contains a mixture of nitroso-nifedipine, oxidized nifedipine, and nifedipine.
  • nitroso-nifedipine, oxidized nifedipine, and nifedipine are mixed at a mass or molar ratio of about 5:1:3, 5:2:2, 6:3:1, 10:4:1, 3:1:5, 2:5:5, or 1:1:1.
  • a therapeutic agent contains a mixture of T3 and T4.
  • T3 and T4 can be mixed at a mass or molar ratio of about 1000:1, about 500:1, about 200:1, about 100:1, about 64:1, about 32:1, about 16:1, about 10:1, about 8:1, about 5:1, about 4:1, about 3:1, about 2:1, about 1 :1, about 1 :2, about 1 :3, about 1 :4, about 1:5, about 1 :8, about 1 : 10, about 1 :16, about 1 :32, about 1 :64, about 1 :100, about 1 :200, about 1 :500, or about 1 :1000.
  • T3 and T4 can be mixed at a mass or molar ratio ranging from about 1 : 1000 to about 1000: 1 (e.g., about 1 :500 to about 500:1, about 1 :200 to about 200:1, about 1 :100 to about 100:1, about 1 :10 to about 10:1, about 1 :16 to about 16:1, about 1 :32 to about 32:1, about 1 :64 to about 64:1, about 1 :1 to about 32:1, about 1 :1 to about 10:1, about 100:1 to about 1000:1, about 10:1 to about 100:1, about 1 :1000 to 1 :1, about 1 :1 to about 1000:1, or about 1 :100 to about 1 :10).
  • a mass or molar ratio ranging from about 1 : 1000 to about 1000: 1 (e.g., about 1 :500 to about 500:1, about 1 :200 to about 200:1, about 1 :100 to about 100:1, about 1 :10 to about 10:1, about 1 :16 to about 16
  • various compounds and mixtures described herein can be further combined to generate desirable therapeutic agents for the invention.
  • a T3/T4 mix can be combined with any of the nifedipine, nifedipine derivatives (e.g., oxidized or nitroso-nifedipine) or nifedipine mixtures described herein.
  • biomarkers can be used to identify subject or patient who is suffering from, susceptible to or at risk of MCI or Alzheimer's disease.
  • a biomarker is a characteristic bio-molecule which is differentially present in a sample taken from a subject of one phenotypic status (e.g., having a disease) as compared with another phenotypic status (e.g., not having a disease).
  • a biomarker is differentially present between different phenotypic statuses if the mean or median expression level of the biomarker in the different groups is calculated to be statistically significant.
  • Biomarkers, alone or in combination provide measures of relative risk that a subject belongs to one phenotypic status or another. Therefore, they are useful as markers for disease (diagnostics), therapeutic effectiveness of a drug (theranostics) and drug toxicity.
  • PDS/TTR complex levels of a ⁇ 55 kDa proteinaceous complex containing prostaglandin-D2-synthase and transthyretin
  • PDS/TTR complex may serve as a sensitive and specific diagnostic biomarker of MCI and AD, as detailed in US Pat. Pub. No. 2008/0026405, which is incorporated herein by reference.
  • the PDS/TTR complex presents in cerebrospinal fluid and appears to be a sensitive and specific biomarker of the disease. Formation of the PDS/TTR complex was been localized to the choroid plexus, an assembly of epithelial cells located adjacent to the lateral ventricles.
  • the choroid plexus functions as the blood-CSF barrier.
  • the choroid plexus passes water, salts and selected small molecules from the blood to the CSF but effectively prevents blood proteins form entering the CSF. Proteins required for CSF are synthesized by the choroid plexus.
  • the choroid plexus also functions as the source of CSF.
  • Epithelial cells isolated from choroid plexus obtained fresh from short post mortem autopsies of late stage AD patients have been grown and expanded in culture. Examination of cell culture medium obtained from AD epithelial cells showed elevated levels of the PDS/TTR complex compared to control cells. Thus, an elevated PDS/TTR complex level as compared to a normal control can be used to identify subjects or patients suffering from, susceptible to or at risk of developing MCI or Alzheimer's disease.
  • a biomarker suitable for the present invention comprises at least one of transthyretin and/or a prostaglandin-H2 D-isomerase, and at least one second protein selected from tranthyretin, prostaglandin-H2 D-isomerase, beta-2-microglobulin, cystatin C, superoxide dismutase [Cu-Zn], plasma retinol-binding protein, phosphatidylethanolamine- binding protein, carbonic anhydrase 2 and/or serotransferrin. Mild cognitive impairment or Alzheimer's disease status is determined by correlating the obtained measurement with standards.
  • neuronal thread protein, tau (total; T-tau and various phosphorylated forms; P-tau), and/or derivatives of amyloid precursor protein (APP) including A ⁇ 4o and A ⁇ 4 2 may be used as biomarkers to identify patient population for treatment with compositions and methods of the present invention.
  • a subject in need of treatment has an abnormal level of a protein biomarker complex as compared to a control, wherein the protein biomarker complex comprises one or more of (i) beta amyloid 40 (A ⁇ 40), (ii) beta amyloid 42 (A ⁇ 42), (iii) the ratio of A ⁇ 40 to A ⁇ 42, and (iv) the ratio of phosphorylated tau to total tau.
  • Additional biomarkers have been reported in the literature and may be used to identify patients for treatment according to the invention including, but not limited to, those described in Fahnestock et al, J. Neural. Transm. Suppl. 2002(62) :241-52 (2002); Masliah et al, Neurobiol. Aging 16(4):549-56 (1995); Power et al, Dement. Geriatr. Cong. Disord. 12(2):167- 170 (2001); Burbach et al, J. Neurosci. 24(10):2421-30 (2004), Li et al, Neuroscience 113(3):607-15 (2002), and Sanna et al, J. Clin. Invest. 111(2):241-50 (2003), each of which is incorporated herein by reference.
  • a biomarker is determined in a fluid sample obtained from the subject.
  • a fluid sample is selected from the group consisting of CSF, serum, whole blood, blood plasma, urine, ascitic fluid, saliva, tissue effusion, lavage, and combinations thereof.
  • ELISA sandwich enzyme linked immunoassay
  • the measured level of a biomarker is compared to one or more controls or reference levels.
  • Suitable reference level used for comparison with the measured level for a AD biomarker may vary, depending on aspect of the invention being practiced, as will be understood by one of ordinary skill in the art.
  • a suitable "reference level” is typically a level indicative of healthy individuals, in particular, age-matched healthy individuals.
  • a reference level can be determined in parallel with patient sample.
  • a reference level can also be a pre-determined level or based on historical data. For example, a suitable reference level can be an average of levels obtained from a population that is not afflicted with AD or MCI.
  • a suitable reference level is derived from (e.g., is the mean or median of) levels obtained from an age-matched population.
  • a subject in need of treatment has an greater or elevated level of a biomarker described herein as compared to a control or reference level indicative of a healthy individual or population.
  • a suitable reference level is typically a level indicative of healthy individuals or individuals suffering from Alzheimer's disease (e.g., with a pre-determined stage, such as MCI, EAD, or LAD).
  • a reference level can be determined in parallel with patient sample.
  • a reference level can also be a pre-determined level or based on historical data.
  • a suitable reference level can be an average of levels obtained from a population that is not afflicted with AD or MCI, or a population that has been diagnosed with MCI or AD (e.g., EAD or LAD).
  • a suitable reference level may be a historical reference level for a particular patient, for example, a level that was obtained from a sample derived from the same individual, but at an earlier point in time (e.g., before the treatment or an earlier point in the treatment).
  • a suitable reference level is derived from (e.g., is the mean or median of) levels obtained from an age-matched population.
  • suitable reference levels are normally derived from (e.g., is the mean or median of) levels obtained from a population which has been diagnosed with a particular stage of AD (e.g., EAD or LAD) or MCI.
  • the level of a suitable biomarker (such as the ⁇ 55 kDa
  • PDS/TTR complex can be used to monitor the efficacy of the treatment.
  • the goal of a therapy would be, ideally, to decrease, lower or diminish the level of the PDS/TTR complex in a subject so that a fluid sample taken from the subject would contain no detectable complex.
  • a more conservative, subsidiary, goal of therapy would be to forestall any increase in the level of the ⁇ 55 kDa PDS/TTR complex. Accordingly, a person of ordinary skill in the medical therapeutic arts would be able to determine whether a given therapeutic regime is accomplishing the chosen therapeutic goal based on the level of an appropriate biomarker.
  • Age-matched populations are ideally the same age as the individual being tested, but approximately age-matched populations are also acceptable. Approximately age-matched populations may be within 1, 2, 3, 4, or 5 years of the age of the individual tested, or may be groups of different ages which encompass the age of the individual being tested. Approximately age-matched populations may be in 2, 3, 4, 5, 6, 7, 8, 9, or 10 year increments (e.g. a "5 year increment" group which serves as the source for reference values for a 62 year old individual might include 58-62 year old individuals, 59-63 year old individuals, 60-64 year old individuals, 61-65 year old individuals, or 62-66 year old individuals).
  • the process of comparing a measured value and a reference value can be carried out in any convenient manner appropriate to the type of measured value and reference value for the AD biomarker at issue.
  • “measuring” can be performed using quantitative or qualitative measurement techniques, and the mode of comparing a measured value and a reference value can vary depending on the measurement technology employed.
  • the measured values used in the methods of the invention will most commonly be quantitative values (e.g., quantitative measurements of concentration, such as nanograms of AD biomarker per milliliter of sample, or absolute amount).
  • the comparison can be made by inspecting the numerical data, by inspecting representations of the data (e.g., inspecting graphical representations such as bar or line graphs).
  • a measured value is generally considered to be substantially equal to or greater than a reference value if it is at least about 95% of the value of the reference value (e.g., a measured value of 1.71 can be considered substantially equal to a reference value of 1.80).
  • a measured value is considered less or lower than a reference value if the measured value is less than 95% of the reference value (e.g., a measured value of 1.7 can be considered less than a reference value of 1.80).
  • MMSE Mini Mental Status Examination
  • CDR Clinical Dementia Rating
  • an MMSE score is used to identify a subject in need of treatment with the compositions and methods described herein.
  • An MMSE score is a composite score representing multiple tests of cognitive function. The maximum possible total MMSE score is 30 points. The MMSE can be used to classify the severity of cognitive impairment in patients with dementia or other medical conditions. Table 1 shows how MMSE scores generally represent degrees of cognitive function.
  • a subject in need of treatment has an MMSE score of 21-
  • a CDR score is used to identify a subject in need of treatment with the compositions and methods described herein.
  • An CDR score is constructed from six domains that are scored individually: memory, orientation, judgment and problem solving, community affairs, home and hobbies, and personal care. Table 2 shows how CDR scores generally represent degrees of cognitive function. Table 2
  • a CDR score above 0 indicates that a subject may be suffering from, susceptible to or at risk of MCI or Alzheimer's disease.
  • a subject in need of treatment may have a CDR score of 0.5 (very mild dementia), 1 (mild dementia), 2 (moderate dementia), or 3 (severe dementia).
  • a cognitive test score (such as an MMSE score or CDR score) can be used to monitor the efficacy of the treatment.
  • an effective therapy should improve the cognitive test score. Therefore, by comparing the cognitive test scores before and after the treatment or from different time points of a treatment regimen, a person of ordinary skill in the medical therapeutic arts can determine whether a given therapeutic regime is effective. For example, a person of ordinary skill in the medical therapeutic arts would be able to determine or adjust the effective amount of a therapeutic agent described herein by based on relative cognitive test scores determined before the treatment or from different time points of a treatment regimen.
  • compositions comprising therapeutic agents such as those disclosed herein.
  • a pharmaceutical composition of the invention contain a therapeutically effective amount of a therapeutic agent and a pharmaceutically acceptable carrier.
  • pharmaceutically acceptable carrier means a non-toxic, inert solid, semi-solid liquid filler, diluent, encapsulating material, formulation auxiliary of any type, or simply a sterile aqueous medium, such as saline.
  • sugars such as lactose, glucose and sucrose, starches such as corn starch and potato starch, cellulose and its derivatives such as sodium carboxymethyl cellulose, ethyl cellulose and cellulose acetate; powdered tragacanth; malt, gelatin, talc; excipients such as cocoa butter and suppository waxes; oils such as peanut oil, cottonseed oil, safflower oil, sesame oil, olive oil, corn oil and soybean oil; glycols, such as propylene glycol, polyols such as glycerin, sorbitol, mannitol and polyethylene glycol; esters such as ethyl oleate and ethyl laurate, agar; buffering agents such as magnesium hydroxide and aluminum hydroxide; alginic acid; pyrogen-free water; isotonic saline, Ringer's solution; ethyl
  • wetting agents such as sodium lauryl sulfate and magnesium stearate, as well as coloring agents, releasing agents, coating agents, sweetening, flavoring and perfuming agents, preservatives and antioxidants can also be present in the composition, according to the judgment of the formulator.
  • antioxidants examples include, but are not limited to, water soluble antioxidants such as ascorbic acid, cysteine hydrochloride, sodium bisulfite, sodium metabisulf ⁇ te, sodium sulfite, and the like; oil soluble antioxidants, such as ascorbyl palmitate, butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), lecithin, propyl gallate, alpha-tocopherol and the like; and the metal chelating agents such as citric acid, ethylenediamine tetraacetic acid (EDTA), sorbitol, tartaric acid, phosphoric acid and the like.
  • water soluble antioxidants such as ascorbic acid, cysteine hydrochloride, sodium bisulfite, sodium metabisulf ⁇ te, sodium sulfite, and the like
  • oil soluble antioxidants such as ascorbyl palmitate, butylated hydroxyanisole (BHA), butylated hydroxytoluen
  • terapéuticaally effective amount refers to an amount of therapeutic agent that is sufficient, when administered to a subject in need of treatment according to an appropriate regimen, to alleviate, ameliorate, stabilize, and/or delay the onset of at least one symptom or feature associated with MCI or Alzheimer's disease as well as delay in progression of one or more symptoms of MCI or Alzheimer's disease (e.g., delay in progression with respect to abundance, intensity, severity, or frequency). It will be understood, however, that the total daily usage of the therapeutic agents and compositions of the present invention will be decided by the attending physician within the scope of sound medical judgment.
  • the specific therapeutically effective dose level for any particular patient will depend upon a variety of factors including the disorder being treated and the severity of the disorder; activity of the specific compound employed; the specific composition employed; the age, body weight, general health, sex and diet of the patient; the time of administration, route of administration, and rate of excretion of the specific compound employed; the duration of the treatment; drugs used in combination or coinciding with the specific compound employed; and like factors well known in the medical arts.
  • a therapeutically effective dose of a therapeutic agent of the present invention can range, for example, from 0.01 to 25 mg/kg body weight or more usually from 0.1 to 15 mg/kg body weight. In some embodiments, a therapeutically effective amount of a therapeutic agent ranges from about 0.01 mg to about 2.5 g per dose (e.g., from about 0.01 mg to about 2.0 g, from about 0.01 mg to about 1.5 g, from about 0.01 mg to about 1.0 g, per dose).
  • a therapeutically effective amount of a therapeutic agent ranges from about 0.01 to about 1000 mg (e.g., about 0.01 to about 500 mg, about 0.01 to about 250 mg, about 0.01 to about 200 mg, about 0.01 to about 150 mg, about 0.01 to about 100 mg, about 0.01 to about 50 mg, about 0.01 to about 10 mg, about 0.01 to about 5 mg, about 0.01 to about 2.5 mg, about 0.01 to about 2.0 mg, about 0.01 to about 1.5 mg, about 0.01 to about 1.0 mg, about 0.01 to about 0.5 mg, about 0.01 to about 0.1 mg) per dose.
  • about 0.01 to about 1000 mg e.g., about 0.01 to about 500 mg, about 0.01 to about 250 mg, about 0.01 to about 200 mg, about 0.01 to about 150 mg, about 0.01 to about 100 mg, about 0.01 to about 50 mg, about 0.01 to about 10 mg, about 0.01 to about 5 mg, about 0.01 to about 2.5 mg, about 0.01 to about 2.0 mg, about 0.01 to about 1.5 mg, about 0.01 to about
  • the therapeutically effective amount of a therapeutic agent ranges from about 100 mg to about 5 g (e.g., about 100 mg to about 3 g, about 100 mg to about 2.5 g, about 100 mg to about 2 g, about 100 mg to about 1.5 g, about 100 mg to about 1000 mg, about 100 mg to about 500 mg, about 100 mg to about 250 mg) per dose.
  • a therapeutically effective amount of a therapeutic agent can be about 0.01 mg, about 0.05 mg, about 0.1 mg, about 0.5 mg, about 1 mg, about 5 mg, about 10 mg, about 25 mg, about 50 mg, about 100 mg, about 500 mg, about 1000 mg, about 1.5 g, about 2 g, about 2.5 g, about 3 g, or about 5 g per dose.
  • the amount described herein is the total amount of all active compounds in a composition.
  • a therapeutically effective amount is the combined amount of nifedipine, nitroso-nifedipine and oxidized nifedipine.
  • a therapeutic agent as described herein is administered once daily. In some embodiments, a therapeutic agent as described herein is administered multiple times per day, e.g., twice, three times, or four times daily. In some embodiments, a total daily dose of a therapeutic agent ranges from about 0.01 mg to about 5 g per day in multiple doses or in a single dose (e.g., from about 0.01 mg to about 4.0 g, from about 0.01 mg to about 3.0 g, from about 0.01 mg to about 2.5 g, from about 0.01 mg to about 2.0 g, from about 0.01 mg to about 1.5 g, from about 0.01 mg to about 1.0 g, per day in multiple doses or in a single dose).
  • a total daily dose of a therapeutic agent ranges from about 0.01 to about 1000 mg (e.g., about 0.01 to about 500 mg, about 0.01 to about 250 mg, about 0.01 to about 200 mg, about 0.01 to about 150 mg, about 0.01 to about 100 mg, about 0.01 to about 50 mg, about 0.01 to about 10 mg, about 0.01 to about 5 mg, about 0.01 to about 2.5 mg, about 0.01 to about 2.0 mg, about 0.01 to about 1.5 mg, about 0.01 to about 1.0 mg, about 0.01 to about 0.5 mg, about 0.01 to about 0.1 mg) per day in a single dose or in multiple doses.
  • about 0.01 to about 1000 mg e.g., about 0.01 to about 500 mg, about 0.01 to about 250 mg, about 0.01 to about 200 mg, about 0.01 to about 150 mg, about 0.01 to about 100 mg, about 0.01 to about 50 mg, about 0.01 to about 10 mg, about 0.01 to about 5 mg, about 0.01 to about 2.5 mg, about 0.01 to about 2.0 mg, about 0.01 to about
  • a total daily dose of a therapeutic agent ranges from about 50 mg to about 5 g (e.g., about 50 mg to about 4 g, about 100 mg to about 3 g, about 100 mg to about 2.5 g, about 100 mg to about 2 g, about 100 mg to about 1.5 g, about 100 mg to about 1000 mg, about 100 mg to about 500 mg, about 100 mg to about 250 mg) per day in a single dose or in multiple doses.
  • a therapeutic agent in particular, nitroso-nifedipine
  • a total daily dose of a therapeutic agent can be about 0.01 mg, about 0.05 mg, about 0.1 mg, about 0.5 mg, about 1 mg, about 5 mg, about 10 mg, about 25 mg, about 50 mg, about 100 mg, about 500 mg, about 1000 mg, about 1.5 g, about 2 g, about 2.5 g, about 3 g, about 3.5 g, about 4 g, about 4.5 g, or about 5 g.
  • an amount described herein is the total amount of all active compounds in a composition.
  • a therapeutically effective amount is the combined amount of nifedipine, nitroso-nifedipine and oxidized nifedipine.
  • a therapeutic agent as described herein is administered monthly, bi-weekly, weekly, twice a week, or three times a week. In these instances, the daily doses described above reflects the average daily dose.
  • the active agent in certain situations, it may be important to maintain a fairly high dose of the active agent in the blood stream of the patient, particularly early in the treatment. Hence, at least initially, it may be important to keep the dose relatively high and/or at a substantially constant level for a given period of time, e.g., at least about six or more hours, e.g., at least about twelve or more hour, e.g., at least about twenty-four or more hours.
  • the compounds of the present invention may be administered alone or in combination or in concurrent therapy with other agents which affect the central or peripheral nervous system, particularly selected areas of the brain.
  • compositions according to the present invention may be administered by any route, including oral, subcutaneous, intravenous, intraperitoneal, intramuscular, intracerebroventricular, intraparenchymal, intrathecal, intracranial, buccal, mucosal, nasal, rectal, auricular, conjunctival, cutaneous, electro-osmosis, endocervical, endosinusial, endotracheal, enteral, epidural, extra-amniotic, extracorporeal, hemodialysis, infiltration, interstitial, intra-abdominal, intra-amniotic, intra-arterial, intra-articular, intrabiliary, introbrochial, intrabursal, intracardiac, intracaritlaginous, intracavitary, intracerebral, intracisternal, intracorneal, intracoronal, intracoronary, intracorporus cavernosum, intradermal, intradiscal, intraductal, intraduodenal, intrad
  • a pharmaceutical composition of the present invention is administered by a route selected from oral, subcutaneous, intravenous, transdermal, intraperitoneal, intramuscular, intracerebroventricular, intraparenchymal, intrathecal, intracranial, buccal, mucosal, nasal, and rectal. In certain embodiments, a pharmaceutical composition of the present invention is administered orally.
  • Liquid dosage forms for oral administration may include pharmaceutically acceptable emulsions, microemulsions, solutions, suspensions, syrups and elixirs containing inert diluents commonly used in the art, such as water, isotonic solutions, or saline.
  • Such compositions may also comprise adjuvants, such as wetting agents; emulsifying and suspending agents; sweetening, flavoring and perfuming agents.
  • Injectable preparations for example, sterile injectable aqueous or oleaginous suspensions may be formulated according to the known art using suitable dispersing or wetting agents and suspending agents.
  • the sterile injectable preparation may also be a sterile injectable solution, suspension or emulsion in a nontoxic parenterally acceptable diluent or solvent, for example, as a solution in 1,3-butanediol.
  • the acceptable vehicles and solvents that may be employed are water, Ringer's solution, U.S. P. and isotonic sodium chloride solution.
  • sterile, fixed oils are conventionally employed as a solvent or suspending medium.
  • any bland fixed oil can be employed including synthetic mono- or diglycerides.
  • fatty acids such as oleic acid are used in the preparation of injectables.
  • the injectable formulation can be sterilized, for example, by filtration through a bacteria-retaining filter, or by incorporating sterilizing agents in the form of sterile solid compositions, which can be dissolved or dispersed in sterile water or other sterile injectable medium just prior to use.
  • the most common way to accomplish this is to inject a suspension of crystalline or amorphous material with poor water solubility.
  • the rate of absorption of the drug becomes dependent on the rate of dissolution of the drug, which is, in turn, dependent on the physical state of the drug, for example, the crystal size and the crystalline form.
  • Another approach to delaying absorption of a drug is to administer the drug as a solution or suspension in oil.
  • Injectable depot forms can also be made by forming microcapsule matrices of drugs and biodegradable polymers, such as polylactide-polyglycoside.
  • the rate of drug release can be controlled.
  • biodegradable polymers include polyorthoesters and polyanhydrides. Depot injectables can also be made by entrapping the drug in liposomes or microemulsions, which are compatible with body tissues.
  • Suppositories for rectal administration of the drug can be prepared by mixing the drug with a suitable non-irritating excipient, such as cocoa butter and polyethylene glycol which are solid at ordinary temperature but liquid at the rectal temperature and will, therefore, melt in the rectum and release the drug.
  • a suitable non-irritating excipient such as cocoa butter and polyethylene glycol which are solid at ordinary temperature but liquid at the rectal temperature and will, therefore, melt in the rectum and release the drug.
  • Solid dosage forms for oral administration include, but are not limited to, capsules, tablets, pills, powders, gelcaps and granules.
  • therapeutic agent may be admixed with at least one inert diluent such as sucrose, lactose or starch.
  • Such dosage forms may also comprise additional substances other than inert diluents, e.g., tableting lubricants and other tableting aids such as magnesium stearate and microcrystalline cellulose.
  • the dosage forms may also comprise buffering agents. Tablets and pills can additionally be prepared with enteric coatings and other release-controlling coatings.
  • compositions of a similar type may also be employed as fillers in soft and hard- filled gelatin capsules using such excipients as lactose or milk sugar as well as high molecular weight polyethylene glycols and the like.
  • the active compounds can also be in micro-encapsulated form with one or more excipients as noted above.
  • the solid dosage forms of tablets, dragees, capsules, pills, and granules can be prepared with coatings and shells such as enteric coatings and other coatings well known in the pharmaceutical formulating art. They may optionally contain opacifying agents and can also be of a composition that they release the active ingredient(s) only, or preferably, in a certain part of the intestinal tract, optionally in a delayed manner. Examples of embedding compositions which can be used include polymeric substances and waxes.
  • Dosage forms for topical or transdermal administration of a compound of this invention further include ointments, pastes, creams, lotions, gels, powders, solutions, sprays, inhalants or patches.
  • the active component is admixed under sterile conditions with a pharmaceutically acceptable carrier and any needed preservatives or buffers as may be required.
  • Ophthalmic formulations, ear drops, eye ointments, powders and solutions are also contemplated as being within the scope of this invention.
  • the ointments, pastes, creams and gels may contain, in addition to an active compound of this invention, excipients such as animal and vegetable fats, oils, waxes, paraffins, starch, tragacanth, cellulose derivatives, polyethylene glycols, silicones, bentonites, silicic acid, talc and zinc oxide, or mixtures thereof.
  • excipients such as animal and vegetable fats, oils, waxes, paraffins, starch, tragacanth, cellulose derivatives, polyethylene glycols, silicones, bentonites, silicic acid, talc and zinc oxide, or mixtures thereof.
  • Powders and sprays can contain, in addition to the active compounds of this invention, excipients such as lactose, talc, silicic acid, aluminum hydroxide, calcium silicates and polyamide powder, or mixtures of these substances.
  • Sprays can additionally contain customary propellants, such as chlorofluorohydrocarbons.
  • Transdermal patches can provide controlled delivery of active compound to the body. Such dosage forms can be made by dissolving or dispersing the compound in the proper medium. Absorption enhancers can also be used to increase the flux of the compound across the skin. The rate can be controlled by either providing a rate controlling membrane or by dispersing the compound in a polymer matrix or gel.
  • compositions described herein can be formulated for immediate release or controlled release (also referred to as slow, sustained or extended release).
  • immediate release or controlled release also referred to as slow, sustained or extended release
  • Various slow or extended release formulations or devices are well known to those of ordinary skill in the art. Examples include, but are not limited to, those described in U.S. Pat. Nos. 5,674,533, 5,059,595, 5,120,548, 5,073,543, 5,639,476, 5,354,556, and 5,733,566, each of which is incorporated herein by reference.
  • Such dosage forms can be used to provide slow or controlled- release of one or more active ingredients using, for example, hydropropylmethyl cellulose, other polymer matrices, gels, permeable membranes, osmotic systems, multilayer coatings, microparticles, liposomes, microspheres, or a combination thereof to provide the desired release profile in varying proportions.
  • Suitable controlled-release formulations known to those of ordinary skill in the art can be readily selected and adapted for use with therapeutic agents of the invention.
  • the invention encompasses solid oral dosage forms such as, but not limited to, tablets, capsules, gelcaps, and caplets that are formulated for controlled-release (i.e., slow release, extended release, or sustained release).
  • controlled-release formulations include extended activity of the drug, reduced dosage frequency, and increased patient compliance.
  • controlled or extended release formulations can keep adequate dose levels constantly available inside a patient body to enhance delivery across the blood-brain barrier.
  • Controlled-release formulations are designed to initially release an amount of therapeutic agent (active ingredient) that promptly produces the desired therapeutic effect, and gradually and continually release of other amounts of thug to maintain this level of therapeutic or prophylactic effect over an extended period of time.
  • the drug In order to maintain this constant level of drug inside the body, the drug must be released from the dosage form at a rate that will replace the amount of drug being metabolized and excreted from the body.
  • Controlled-release of an active ingredient can be stimulated by various conditions including, but not limited to, pH, temperature, enzymes, water, or other physiological conditions or compounds.
  • two or more therapeutic agents may be administered in combination.
  • the two or more therapeutic agents may be administered separately from one another, as part of a multiple dosage regimen.
  • those agents may be part of a single dosage form, mixed together with a compound of this invention in a single composition. If administered as part of a multiple dosage regime, the two therapeutic agents may be submitted simultaneously, sequentially or within a period of time from one another normally within five hours from one another.
  • the term “combination,” “combined,” and related terms refers to the simultaneous or sequential administration of therapeutic agents in accordance with this invention.
  • a compound of the present invention may be administered with another therapeutic agent simultaneously or sequentially in separate unit dosage forms or together in a single unit dosage form.
  • the present invention provides a single unit dosage form comprising a provided compound, an additional therapeutic agent, and a pharmaceutically acceptable carrier, adjuvant, or vehicle.
  • the invention is provided in numerous embodiments and can be discerned, inter alia, in various examples.
  • the following examples provide an illustrative but non-limiting description of the breadth and applicability of the invention.
  • acrolein an alpha, beta unsaturated three carbon aldehydic by-product of lipid peroxidation
  • acrolein causes normal control epithelial cells to express the PDS/TTR complex into culture medium at comparable levels to the epithelial cells derived from Alzheimer's disease patients.
  • primary cultures of choroid plexus epithelail cells were established from short post mortem interval autopsies using established methods. AD and normal control cultures were grown to confluence in MEM growth medium containing 2% fetal bovine serum and 1% epithelial growth factor (EGF).
  • EGF epithelial growth factor
  • FIG. 1 shows exemplary results illustrating an Western blot analysis of the PDS/TTR complex expressed in cell culture medium by control epithelial cells, control epithelial cells treated with acrolein, and epithelial cells derived from late stage Alzheimer's disease patients.
  • acrolein increased the expression of the PDS/TTR complex in control epithelial cells to a level comparable to that in late stage AD (LAD) epithelial cells.
  • SY5Y neuroblastoma cells were exposed to conditioned medium from LAD or normal control epithelial cells for 16 hours. Following exposure to conditioned medium, cells were fixed in 70% methanol/30% acetone and were subjected to immunohistochemistry using anti-PHF-1 antibody.
  • PHF-I recognizes aberrantly phosphorylated Tau as observed in AD NFT (neurofibrillary tangles).
  • AD NFT neuroofibrillary tangles
  • close to 25% of SY5Y cells treated with LAD epithelial cell medium are PHF-I positive as compared to about 3% of SY5Y cells treated with control medium. Paired helical filaments are precursors to neurofibrillary tangles.
  • PHFl immunopositivity is typically an indicator of the formation of late-stage neurofibrillary tangles in Alzheimer's disease.
  • this experiment shows that the PDS/TTR complex promotes the formation of paired helical filaments in SY5Y neuroblastoma cells, indicating the PDS/TTR that complex can promote amyloid beta peptide (AB) generation by H4 neuroglioma cells.
  • AB amyloid beta peptide
  • PDS/TTR complex causes various biochemical changes that can directly impact hallmarks of Alzheimer's disease.
  • Example 1 The assays described in Example 1 provide a tool to identify potential therapeutic agents that can protect neuronal cells against the PDS/TTR complex.
  • compounds such as nifedipine (l,4-dihydro-2,6-dimethyl-4-(2-nitrophenyl)-3,5- pyridinydicarboxylic acid dimethyl ester, CAS#21829-25-4 (Sigma Aldrich)), a calcium channel blocker prescribed for high blood pressure; or nifedipine analogs such as oxidized derivative of nifedipine ((2,6-dimethyl-4-(2-nitrophenyl)- 3,5-pyridinedicarboxylic acid dimethyl ester, CAS# 67035-22-7 (Sigma Aldrich)) or a nitroso derivative of nifedipine (2,6-dimethyl-4-(2- nitrosophenyl)- 3,5-pyridinedicarboxylic acid dimethyl ester, CAS#50428-14-3 (S
  • T3 and T4 were also evaluated and found to be effective in inhibiting the expression of PDS/TTR complex.
  • epithelial cells were treated with 5 ⁇ M acrolein, 5 ⁇ M acrolein plus
  • Alzheimer's disease patients The inventors tested the nifedipine mix and individual analogs in astrocytoma cultures. Human astrocytoama cells were plated at 2.5 X lO 5 cells/well in 6 well culture plates and were grown for 24 hours. Cultures were then switched to serum free Opti- MEM and treated with the nifedipine mixture and individual analogs for 24 hours. Three 6-well plates were subjected to each treatment. Following treatment, medium was collected from each well and levels of IL-IB, IL-6, TNF- ⁇ and TGF-B were measured using commercially available ELISAs. Exemplary results are shown in Figure 7.
  • IL-I, IL-6 and TNF- ⁇ secreted in the medium were significantly reduced with the treatment of nifedipine mix or oxidized nifedipine, indicating these compounds have a direct positive effect on neuroinflammation.
  • LAD epithelial cells that contained significantly higher levels of the PDS/TTR complex displayed significantly increased PHF-I immunostaining as compared to those exposed to medium from untreated control cultures.
  • SY5Y cells were exposed to medium from epithelial cells treated with acrolein and combinations of nifedipine, nifedipine analogs, mixtures of nifedipine analogs and T3/T4 using procedures described in Example 1.
  • nifedipine mix and nifedipine/nifedipine analogs plus T3/T4 significantly reduced PHF-I levels.
  • Example 5 Inhibition of A ⁇ 1-42 production from H4 neuroglioblastoma cells
  • H4 neuroglioblastoma cells stably transfected to overexpress amyloid precursor protein (APP) to further investigate if nifedipine, nifedipine analogs (e.g., oxidized nifedipine or nitroso-nifedipine) and/or T3/T4 can inhibit the production of A ⁇ 1-42.
  • H4 neuroglioblastoma cells stably transfected with a construct overexpressing amyloid precursor protein (APP) secret ABi_ 42 into the culture medium.
  • H4 cells were treated with 1 ⁇ M fresh nifedipine, 1 ⁇ M oxidized nifedipine, 1 ⁇ M nitroso-nifedipine, or 0.5 ⁇ M T3/0.5 ⁇ M T4 for 16 hours.
  • the AB levels in the culture medium were measured using ELISAs (Invitrogen). As shown in Figure 9, treatment of fresh nifedipine, oxidized nifedipine, nitroso- nifedipine, or T3/T4 lead to significantly decreased production of AB 1-42.
  • T3/T4 improves the inhibitory effect of nifedipine, nifedipine analogs and nifedipine mix on AB 1-42 production.
  • Nicardipine showed a trend (p ⁇ 0.10) toward a significant decrease in AB secretion and Nimodipine led to a significant (p ⁇ 0.05) decrease in AB formation.
  • the other drugs did not significantly alter levels of AB formation.
  • Combining the alternate calcium channel blockers with T3/T4 showed a significant decrease of AB formation when T3/T4 were combined with Amlodipine and Dilitiazem.
  • Combinations of T3/T4 with the other drugs did not provide any significant decrease in AB formation.
  • Example 6 Inhibition of beta secretase (BACE) and gamma secretase activity
  • a ⁇ i_4 2 production depends on the activity of beta secretase (BACE), an enzyme that cleaves the amyloid precursor protein at the beta secretase cleavage site, and the gamma secretase complex composed of presenilin-1 (PS- 1), nicastrin, APH-I and PEN-2 that cleaves at the gamma secretase cleavage site.
  • BACE beta secretase
  • BACE activity was measured using a fluorescent substrate and purified recombinant BACE as part of a commercial kit from Invitrogen. As shown in Figure 12, nifedipine alone or in combination with thyroxine slightly inhibited BACE activity; however, nitroso-nifedipine alone and in combination with thyroxine led to significant inhibition of BACE activity (Figure 12).
  • C57BL/6 mice were subjected to intraperitoneal (IP) injections of vehicle (2%DMSO/98% polyethylene glycol-3000 (PEG-3000), 25 mg/kg nifedipine or nifedipine mix, T3/T4 (10 mg/kg T3 and 10 mg/kg T4), nifedipine mix plus T3/T4 and nifedipine plus T3/T4 on three consecutive days. Animals were euthanatized 1 hour after the third injection. The brains and terminal serum were removed and immediately frozen in liquid nitrogen and stored at -80 0 C until used for analysis.
  • vehicle 2%DMSO/98% polyethylene glycol-3000 (PEG-3000)
  • T3/T4 10 mg/kg T3 and 10 mg/kg T4
  • T3/T4 10 mg/kg T3 and 10 mg/kg T4
  • mice treated with both T3/T4 and nifedipine mix plus T3/T4 showed a modest (25%) but significant decrease in A ⁇ i_ 40 levels compared to animals treated with vehicle.
  • levels of PS-I, Nicast, and APH-I were significantly decreased in mice treated with nifedipine, nifedipine mix plus T3/T4.
  • BACE protein levels were significantly decreased in mice treated with nifedipine, nifedipine plus T3/T4 and T3/T4 alone. In contrast, there were no significant differences in levels of cleaved Notch with any treatment ( Figure 14).
  • nifedipine was found in all samples analyzed indicating that components of the mixture were passing the blood-brain barrier and thus available for neuronal protection. This experiments has shown that these derivatives possess the brain permeability desired for treatment of Alzheimer's disease.
  • T3/T4 can inhibit the orphan G-coupled receptor protein 3 (GPCR-3), an enzyme which is suggested to play a role in maintaining stability of the gamma secretase complex (which, as discussed above, is important for cleavage of APP to form A ⁇ ).
  • GPCR-3 G-coupled receptor protein 3
  • H4 neuroglioblastoma cells were treated with 1 ⁇ M mixed nifedipine, 1 ⁇ M mixed nifedipine plus 0.5 ⁇ M T3/0.5 ⁇ M T4, 0.5 ⁇ M T3/0.5 ⁇ M T4, 1 ⁇ M fresh nifedipine, 1 ⁇ M fresh nifedipine plus 0.5 ⁇ M T3/0.5 ⁇ M T4 for 16 hours.
  • Levels of GPCR-3 were measured using Western blot analysis using a GPCR-3 specific antibody. As shown in Figure 15, nifedipine mixtures, fresh nifedipine, and/or T3/T4 significantly reduced GPCR-3 expression levels in H4 cells.
  • GPCR-3 levels were determined in the C57BL/6 mice described above in Example 7 using Western blot analysis. Exemplary results are also shown in Figure 15. Nifedipine mixtures and T3/T4, fresh nifedipine, and T3/T4 also reduced GPCR-3 expression levels in mice.
  • nifedipine, nifedipine mixtures, their oxidized and nitroso derivatives, and/or T3/T4 can reduce phosphorylated Tau protein.
  • Phosphorylated tau protein can result in the self-assembly of tangles of paired helical filaments and straight filaments, which are involved in the pathogenesis of Alzheimer's disease.
  • GSK-3 ⁇ glycogen synthase kinase-3B
  • Akt protein kinase B
  • Akt a serine/threonine kinase is regulated by phosphatidylinositol kinase (PI3K) mediated signaling and is activated by phosphorylation of a regulatory threonine residue (Thr-308) by phosphatidylinositol dependent kinase 1 (PDKl) and by phosphorylation of Ser 473 by PDK ⁇ /TORC2 kinase.
  • PI3K phosphatidylinositol kinase
  • PDKl phosphatidylinositol dependent kinase 1
  • Ser 473 by PDK ⁇ /TORC2 kinase.
  • activation of the Akt/GSK- 3 ⁇ pathway may be mediated by GCPRs coupled to G ⁇ l2/13 heterotrimeric G proteins. Activation of G ⁇ i2 has been shown to stimulate RhoA and its effector Rho kinase (ROCK).
  • ROCK phosphorylated at ser 160 further transactivates a receptor tyrosine kinase (RTK) that activates the PI3K signaling pathway leading to phosphorylation/activation of Akt/GSK-3 ⁇ (reviewed by New et al, "G protein-coupled receptor-induced Akt activity in cellular proliferation and apoptosis," FEBSJ, 2007; 274:6025-36.).
  • RTK receptor tyrosine kinase
  • Phosphoryalted Akt increases phosphorylation and inactivation of GSK-3 ⁇ therefore reducing Tau phosphorylation.
  • dihydropyridine calcium channel blockers appears to delay the onset of cognitive decline, suggesting dihydropyridine calcium channel blockers can be used to treat neurodegenerative diseases such as Alzheimer's disease.
  • a ⁇ 1-42 and A ⁇ processing enzymes such as PS-I, Nicas, BACE, APH-I and PEN-2 in front lobe specimens of subjects were determined using standard methods. Specifically, A ⁇ l-42 levels were determined using Invitrogen ELISAs and protein levels were determined using Western blot analysis and antibodies specific to each protein. As shown in Figure 18, the A ⁇ l-42 level was significantly reduced in subjects with drugs as compared to that in subjects without drugs. Some A ⁇ processing enzymes including PS-I, Nicas were significantly reduced in those subjects with drugs as compared to those without drugs. Interestingly, the levels of BACE, APH-I and PEN-2 were increased in those subjects with drugs as compared to subjects without drugs.
  • nifedipine (20 mg) was dissolved in 10 mL acetonitrile in a pyrex culture tube, capped and photolyzed with a 250W halogen lamp (3M EVW) for 30 minutes. The product was isolated by solvent removal on a rotary evaporator to obtain a blue-green oil (18.1 mg, 94% yield). GC/MS analysis showed greater than 98.5% conversion to nitrosonifedipine. An exemplary result is shown in Figure 20.
  • a human patient determined to have MCI based on an MMSE score is given nitroso-nifedipine at a dosage of 1000 mg per day. Nitroso-nifedipine is given as tablets for oral administration by patient three times daily.
  • nitroso-nifedipine Another human patient determined to have early stage Alzheimer's disease (EAD) based on a CDR score is given nitroso-nifedipine at a dosage of 800 mg per day. Nitrosonifedipine is given as tablets for oral administration by patient three times daily. [0191] A human patient determined to have MCI based on the level of PDS/TTR complex in a fluid sample obtained from the patient is given nitroso-nifedipine at a dosage of 1000 mg per day. Nitroso-nifedipine is given as tablets for oral administration by patient four times daily.
  • EAD early stage Alzheimer's disease
  • the invention encompasses all variations, combinations, and permutations in which one or more limitations, elements, clauses, descriptive terms, etc., from one or more of the claims or from relevant portions of the description are introduced into another claim.
  • any claim that is dependent on another claim can be modified to include one or more limitations found in any other claim that is dependent on the same base claim.
  • the claims recite a composition, it is to be understood that methods of using the composition for any of the purposes disclosed herein are included, and methods of making the composition according to any of the methods of making disclosed herein or other methods known in the art are included, unless otherwise indicated or unless it would be evident to one of ordinary skill in the art that a contradiction or inconsistency would arise.
  • the invention encompasses compositions made according to any of the methods for preparing compositions disclosed herein.

Landscapes

  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

The present invention provides, among other things, therapeutic compositions and methods that can effectively treat, slow or prevent mild cognitive impairment (MCI) or Alzheimer's disease (AD), in particular, based on therapeutically effective amount of nifedipine, oxidized or nitroso nifedipine derivatives, thyroxine (T4), triiodothyronine (T3) and combinations thereof.

Description

TREATMENT OF MCI AND ALZHEIMER'S DISEASE
REFERENCE TO RELATED APPLICATION
[0001] This application claims the benefit of U.S. Provisional Patent Application No.
61/216,452, filed May 15, 2009, and U.S. Provisional Patent Application No. 61/234,551, filed August 17, 2009, both of which are hereby incorporated by reference in their entireties.
BACKGROUND OF THE INVENTION
[0002] Alzheimer's disease (AD) is a well-known but incompletely understood progressive neurodegenerative disease affecting ever-larger numbers of individuals in the aging population. Currently Alzheimer's disease affects 4 million Americans. Statistics from the National Institute on Aging estimate that there may be 14 million Americans with Alzheimer's disease by 2040 unless preventative strategies are developed.
[0003] The earliest clinical manifestation of Alzheimer's disease is described as a syndrome called Mild Cognitive Impairment (MCI). While detection of MCI may permit necessary lifestyle modifications to be planned and implemented, no therapies are currently available that forestall the progression of MCI to Alzheimer's disease or to treat Alzheimer's disease.
[0004] In 2007 testimony before the US Senate, FDA Commissioner Dr. Andrew C. von
Eschenbach stated that "the estimated 4.5 million cases of Alzheimer's today can be expected to rise to about 16 million by 2050." Dr. Eschenbach explained that five drugs were approved for AD treatment — tacrine, rivastigmine, galantamine, donepezil, and memantine — the first four of which act by elevating acetylcholine levels in the brain, and the last of which is an antagonist of the N-methyl-D-aspartate receptor. Thus, Dr. Eschenbach pointed out that none of the five approved drugs have been shown to prevent or slow the underlying nerve degeneration in [AD] patients. He continued: "We await, together with the rest of the world, [] new drugs that may some day be able to treat the underlying cause of this insidious disease as well as other neurological diseases . . ."
SUMMARY OF THE INVENTION
[0005] The present invention encompasses the discovery that nifedipine and its oxidized or nitroso derivatives can effectively inhibit Aβl-40 generation, reduce Aβ processing enzymes and inactivate related biochemical pathways, both in vitro and in vivo. Thus, the present invention provides, among other things, novel therapeutic methods and compositions that can effectively treat, slow or prevent Mild Cognitive Impairment (MCI) and/or Alzheimer's disease, as well as delaying the progression from MCI to AD.
[0006] In one aspect, the present invention provides a pharmaceutical composition suitable for treating, slowing, or preventing Mild Cognitive Impairment (MCI) and/or Alzheimer's disease in a human subject comprising a therapeutically effective amount of one or more therapeutic agents and a pharmaceutically acceptable carrier. In some embodiments, a therapeutic agent is of formula (Ia) as defined and described herein. In some embodiments, a therapeutic agent is of formula (Ib) as defined and described herein. In some embodiments, a therapeutic agent suitable for the invention is selected from the group consisting of nifedipine, oxidized nifedipine, nitroso-nifedipine, thyroxine (T4), triiodothyronine (T3) and combinations thereof. In some embodiments, a therapeutic agent suitable for the invention is a calcium channel blocker. In some embodiments, a therapeutic agent suitable for the invention is not a calcium channel blocker.
[0007] In some embodiments, a therapeutic agent suitable for the invention comprises nifedipine. In some embodiments, a therapeutic agent suitable for the invention comprises oxidized nifedipine. In some embodiments, a therapeutic agent suitable for the invention comprises nitroso-nifedipine. In some embodiments, a therapeutic agent suitable for the invention comprises a mixture of nitroso-nifedipine, oxidized nifedipine, and nifedipine. In some embodiments, a therapeutic agent suitable for the invention comprises 55% nitroso- nifedipine, 11% oxidized nifedipine, and 34% nifedipine. In some embodiments, various therapeutic agents described herein further comprises thyroxine (T4) and/or triiodothyronine (T3). In some embodiments, a therapeutic agent suitable for the invention comprises nifedipine, oxidized nifedipine, nitroso-nifedipine, thyroxine (T4) and/or triiodothyronine (T3).
[0008] In some embodiments, a pharmaceutical composition according to the present invention comprises a therapeutic agent in a therapeutically effective amount of about 0.01 to about 1000 mg (e.g., about 0.01 to about 200 mg, about 0.01 to about 100 mg, about 0.1 to about 50 mg, about 0.01 to about 10 mg, about 0.01 to about 5 mg, about 0.01 to about 2.5 mg, about 0.01 to about 2.0 mg, about 0.01 to about 1.5 mg, about 0.01 to about 1.0 mg, about 0.01 to about 0.5 mg, about 0.01 to about 0.1 mg) per dose. In some embodiments, a pharmaceutical composition according to the present invention comprises nitroso-nifedipine in a therapeutically effective amount of about 10 mg to 2.5 g (e.g., about 10 mg to 2.0 g, about 10 mg to 1.5 g, about 10 to about 1000 mg, about 10 mg to about 500 mg) per dose. In some embodiments, a pharmaceutical composition according to the present invention is formulated for oral, subcutaneous, intravenous, transdermal, intraperitoneal, intramuscular, intracerebroventricular, intraparenchymal, intrathecal, intracranial, buccal, mucosal, nasal, or rectal administration. In certain embodiments, a pharmaceutical composition according to the present invention is formulated for oral administration. In some embodiments, a pharmaceutical composition according to the invention is formulated for immediate or extended release.
[0009] In another aspect, the present invention provides a method for treating, slowing, or preventing Mild Cognitive Impairment (MCI) and/or Alzheimer's disease in a human subject, the method comprising administering to a subject who is suffering from or susceptible to MCI or Alzheimer's disease a therapeutically effective amount of one or more therapeutic agents, such that at least one symptom or feature associated with the MCI or Alzheimer's disease is reduced in abundance, intensity, severity, or frequency, or has delayed onset. In some embodiments, a symptom or feature is cognitive decline, production of amyloid beta protein, beta-secretase activity, gamma-secretase activity, paired helical filaments, phosphorylated tau protein in the brain, and/or an immune or inflammatory condition in the central nervous system. In some embodiments, the gamma-secretase activity is reduced by inhibiting presenilin-1 (PS-I), nicastrin, APH-I and/or PEN-2 activity. In some embodiments, the gamma-secretase activity is reduced by inhibiting orphan G-coupled receptor 3 (GPCR-3) activity. In some embodiments, an immune or inflammatory condition is reduced by decreasing the level of one or more cytokines (e.g., IL-I, IL-6, TNF-α) in the central nervous system.
[0010] In some embodiments, a therapeutic agent used in a method according to the present invention is of formula (Ia) as defined and described herein. In some embodiments, a therapeutic agent used in a method according to the invention is of formula (Ib) as defined and described herein. In some embodiments, a suitable therapeutic agent is selected from the group consisting of nifedipine, oxidized nifedipine, nitroso-nifedipine, thyroxine (T4), triiodothyronine (T3) and combinations thereof. In some embodiments, a suitable therapeutic agent is a calcium channel blocker. In some embodiments, a suitable therapeutic agent is not a calcium channel blocker.
[0011] In some embodiments, a suitable therapeutic agent comprises nifedipine. In some embodiments, a suitable therapeutic agent comprises oxidized nifedipine. In some embodiments, a suitable therapeutic agent comprises nitroso-nifedipine. In some embodiments, a suitable therapeutic agent used in a method according to the present invention comprises a mixture of nitroso-nifedipine, oxidized nifedipine, and nifedipine. In some embodiments, a suitable therapeutic agent used in a method according to the present invention comprises 55% nitroso- nifedipine, 11% oxidized nifedipine, and 34% nifedipine. In some embodiments, suitable agents described herein further comprises T3/T4. In some embodiments, an suitable agent used in a method of the present invention comprising nifedipine, oxidized nifedipine, and/or nitroso- nifedipine further comprises thyroxine (T4) and/or triiodothyronine (T3).
[0012] In some embodiments, a method according to the present invention administers to a subject in need of treatment a therapeutic agent in a therapeutically effective amount of about 0.01 to about 1000 mg (e.g., about 0.01 to about 200 mg, about 0.01 to about 100 mg, about 0.1 to about 50 mg, about 0.01 to about 10 mg, about 0.01 to about 5 mg, about 0.01 to about 2.5 mg, about 0.01 to about 2.0 mg, about 0.01 to about 1.5 mg, about 0.01 to about 1.0 mg, about 0.01 to about 0.5 mg, about 0.01 to about 0.1 mg) per dose. In some embodiments, a method according to the present invention administers to a subject in need of treatment a therapeutic agent comprising nitroso-nifedipine in a therapeutically effective amount of about 10 mg to about 2.5 g (e.g., about 10 mg to about 2.0 g, about 10 mg to about 1.5 g, about 10 mg to about 1000 mg, or about 10 mg to about 500 mg) per dose. In some embodiments, an agent used in a method according to the present invention is administered by oral, subcutaneous, intravenous, transdermal, intraperitoneal, intramuscular, intracerebroventricular, intraparenchymal, intrathecal, intracranial, buccal, mucosal, nasal, or rectal administration. In certain embodiments, an agent used in a method according to the present invention is administered orally.
[0013] In some embodiments, according to a method of the present invention, an agent is administered monthly, bi-weekly, or weekly. In some embodiments, according to a method of the present invention, an agent is administered daily. In some embodiments, according to a method of the present invention, an agent is administered twice daily, three times daily, or four times daily.
[0014] In some embodiments, a subject treated by a method of the present invention has a diminished or elevated level of a biomarker (e.g., a protein biomarker complex) as compared to a control. In some embodiments, a suitable biomarker is a protein biomarker complex comprising at least one of a transthyretin protein and/or a prostaglandin-H2 D-isomerase protein, and at least one second, different protein selected from a transthyretin, prostaglandin-H2 D- isomerase, beta-2-microglobulin, cystatin C, superoxide dismutase [Cu-Zn], plasma retinol- binding protein, phosphatidylethanolamine -binding protein, carbonic anhydrase 2, and/or serotransferrin protein. In some embodiments, a suitable protein biomarker complex comprises prostaglandin-D2-synthase and transthyretin (PDS/TTR complex). In some embodiments, a suitable biomarker comprises one or more of (i) beta amyloid 40 (Aβ40), (ii) beta amyloid 42 (Aβ42), (iii) the ratio of Aβ40 to Aβ42, and (iv) the ratio of phosphorylated tau to total tau. In some embodiments, a biomarker is determined in a fluid sample (e.g., CSF, serum, whole blood, blood plasma, urine, ascitic fluid, saliva, tissue effusion, lavage, and combinations thereof) obtained from the subject. In some embodiments, a suitable control is indicative of a level of the biomarker in a subject selected from the group consisting of a healthy individual, a patient suffering from Alzheimer's disease with a pre-determined stage, the subject before the treatment, and combinations thereof. [0015] In some embodiments, a subject to be treated has a test score indicative of cognitive impairment. In some embodiments, a test score indicative of cognitive impairment is an MMSE score (e.g., lower than 27, e.g., 21-26). In some embodiments, a test score indicative of cognitive impairment is a CDR score (e.g., above 0, e.g., 0.5, e.g., 1).
[0016] In some embodiments, a method according to the invention further includes a step of first determining the therapeutically effective amount of the therapeutic agent based on the level of a biomarker and/or a cognitive test score.
[0017] In yet another aspect, the invention provides a solid oral dosage form comprising nitroso-nifedipine and nifedipine, and wherein the mass ratio of nitroso-nifedipine to nifedipine is at least about 1 :1 (e.g., at least about 2:1, at least about 4:1, at least about 8:1, at least about 16:1, at least about 32:1, at least about 64:1, at least about 100:1, at least about 200:1, at least about 500:1, or at least about 1000:1). In some embodiments, a solid oral dosage form according to the present invention further comprises one or more pharmaceutically acceptable excipients (e.g., a binder, a buffer, a diluent, a dispersant, an emollient, a film-forming agent, a glidant, a light-blocking agent, a preservative, a solvent, a stabilizing agent, a surfactant, a suspending agent, and/or a tonicity agent). In some embodiments, a solid dosage form is for controlled or extended release. In some embodiments, a solid dosage form is for immediate release.
[0018] In this application, the use of "or" means "and/or" unless stated otherwise. As used in this application, the term "comprise" and variations of the term, such as "comprising" and "comprises," are not intended to exclude other additives, components, integers or steps. As used in this application, the terms "about" and "approximately" are used as equivalents. Any numerals used in this application with or without about/approximately are meant to cover any normal fluctuations appreciated by one of ordinary skill in the relevant art. BRIEF DESCRIPTION OF THE DRAWINGS
[0019] The drawings are for illustration purposes only and not for limitation.
[0020] Figure 1 illustrates an exemplary Western blot analysis of the PDS/TTR complex expressed in cell culture medium by control epithelial cells, control epithelial cells treated with acrolein, and late stage AD epithelial cells.
[0021] Figure 2 illustrates exemplary survival data for cortical neurons treated with medium from control epithelial cells or AD epithelial cells.
[0022] Figure 3 illustrates exemplary results indicating that PHFl immunopositivity was detected in SY5Y cells resulting from exposure to the PDS/TTR protein complex.
[0023] Figure 4 illustrates exemplary Western blot data showing reduction of the
PDS/TTR complex expressed by control epithelial cells treated with acrolein, acrolein plus T3/T4, acrolein plus nifedipine mixture (nitroso nifedipine 55%, oxidized nifedipine 11% and nifedipine 34%) and acrolein plus nifedipine mix and T3/T4.
[0024] Figure 5 summarizes the numbers of PDS/TTR-positive cells determined by immunostaining in cultures treated with acrolein, acrolein plus T3/T4, acrolein plus nifedipine mixture (nitroso nifedipine 55%, oxidized nifedipine 11% and nifedipine 34%) and acrolein plus nifedipine mix and T3/T4.
[0025] Figure 6 illustrates that nifedipine mix does not function as a calcium channel blocker compared to fresh nifedipine as determined by confocal microscopy and a calcium fluorescent dye.
[0026] Figure 7 illustrates exemplary results indicating that inflammatory cytokine production was inhibited by nifedipine mix.
[0027] Figure 8 illustrates quantification of PHF-I immunostaining for SY5Y cultures treated with medium from epithelial cells treated with acrolein and combinations of nifedipine, analogs, mixtures and T3/T4. [0028] Figure 9 illustrates exemplary results indicating that ABi_42 generation is inhibited by nifedipine, oxidized nifedipine, nitroso nifedipine and T3/T4.
[0029] Figure 10 illustrates exemplary results indicating effect of nifedipine, nifedipine analogs and nifedipine mix, with and without T3/T4 on Aβ i_42 production from H4 cells.
[0030] Figure 11 illustrates exemplary results indicating effects of known calcium channel blockers such as Amilodpine, Dilitiazem, Felodipine, Isradipine, Nicardipine, and Nimodipine on Aβ 1-42 generation in H4 neuroglioma cultures.
[0031] Figure 12 illustrates exemplary results indicating that nitroso-nifedipine significantly inhibits BACE activity.
[0032] Figure 13 illustrates exemplary results indicating the effect of nifedipine mix on
PS-I, PEN-2, BACE-I and Nicastrin, with and without T3/T4.
[0033] Figure 14 illustrates exemplary results indicating the effect of nifedipine, nifedipine mix and/or T3/T4 on AB 1-40 generation and certain AB 1-40 processing enzymes in a mouse model.
[0034] Figure 15 illustrates exemplary results indicating that nifedipine, nifedipine mix and/or T3/T4 reduced GPCR-3 levels in H4 cultures or in mice treated acutely with drugs. The GPCR-3 levels were determined using Western blot analysis.
[0035] Figure 15a illustrates exemplary results indicating the effect of other classes of blood pressure drugs on the levels of GPCR-3 in H4 cultures with and without T3/T4.
[0036] Figure 16 illustrates exemplary results indicating the effect of nifedipine, nifedipine mix and/or T3/T4 on the levels of enzymes involved in Tau phosphorylation measured in the mouse brains treated with corresponding compounds.
[0037] Figure 17 illustrates exemplary trajectories fitted according to the NLMIXED model of MMSE verse age based on a human association study. [0038] Figure 18 illustrates exemplary results indicating levels of Aβ 1-42 and Aβ processing enzymes such as PS-I, Nicas, BACE, APH-I and PEN-2 in front lobe specimens of subjects from a neuropsychological test score association study who came to autopsy. 4 subjects were on calcium channel blockers, including nifedipine and 4 subjects were not on any calcium channel blocker. AB levels determined using Invitrogen ELISAs. Protein levels determined using Western blot analysis and antibodies specific to each protein.
[0039] Figure 19 illustrates exemplary results indicating enzyme levels involved in Tau phosphorylation in frontal lobe specimens from the same subjects shown in Figure 18.
[0040] Figure 20 illustrates exemplary results from a photochemical synthesis of nitroso- nifedipine.
DEFINITIONS
[0041] Unless defined otherwise, the scientific and technological terms and nomenclature used herein have the same meaning as commonly understood by a person of ordinary skill to which this invention pertains. Generally, the procedures of cell cultures, infection, molecular biology methods and the like are common methods used in the art. Such standard techniques can be found in reference manuals such as, for example, Ausubel et ah, Current Protocols in Molecular Biology, Wiley Interscience, New York, 2001; and Sambrook et al., Molecular Cloning: A Laboratory Manual, 3rd edition, Cold Spring Harbor Laboratory Press, N.Y., 2001.
[0042] In order for the present invention to be more readily understood, certain terms are first defined. Additional definitions for the following terms and other terms are set forth throughout the specification.
[0043] Alzheimer's patient: As used herein, the terms "Alzheimer's patient," "AD patient," and "individual diagnosed with AD" all refer to an individual who has been diagnosed with AD or has been given a probable diagnosis of Alzheimer's Disease (AD). [0044] Animal: As used herein, the term "animal" refers to any member of the animal kingdom. In some embodiments, "animal" refers to humans, at any stage of development. In some embodiments, "animal" refers to non-human animals, at any stage of development. In certain embodiments, the non-human animal is a mammal (e.g., a rodent, a mouse, a rat, a rabbit, a monkey, a dog, a cat, a sheep, cattle, a primate, and/or a pig). In some embodiments, animals include, but are not limited to, mammals, birds, reptiles, amphibians, fish, insects, and/or worms. In some embodiments, an animal may be a transgenic animal, genetically-engineered animal, and/or a clone.
[0045] Approximately: As used herein, the term "approximately" or "about," as applied to one or more values of interest, refers to a value that is similar to a stated reference value. In certain embodiments, the term "approximately" or "about" refers to a range of values that fall within 25%, 20%, 19%, 18%, 17%, 16%, 15%, 14%, 13%, 12%, 11%, 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2%, 1%, or less in either direction (greater than or less than) of the stated reference value unless otherwise stated or otherwise evident from the context (except where such number would exceed 100% of a possible value).
[0046] Biological fluid sample: As used herein, the term "biological fluid sample" encompasses a variety of fluid sample types obtained from an individual and can be used in a diagnostic or monitoring assay. The term encompasses whole blood, blood serum or blood plasma, cerebrospinal fluid (CSF), urine and other liquid samples of biological origin. The term also includes samples that have been manipulated in any way after their procurement, such as by treatment with reagents, solubilization, or enrichment for certain components, such as proteins or polynucleotides.
[0047] Combination therapy: The term "combination therapy", as used herein, refers to those situations in which two or more different pharmaceutical agents are administered in overlapping regimens so that the subject is simultaneously exposed to both agents.
[0048] Control: As used herein, the term "control" has its art-understood meaning of being a standard against which results are compared. Typically, controls are used to augment integrity in experiments by isolating variables in order to make a conclusion about such variables. In some embodiments, a control is a reaction or assay that is performed simultaneously with a test reaction or assay to provide a comparator. In one experiment, the "test" (i.e., the variable being tested) is applied. In the second experiment, the "control," the variable being tested is not applied. In some embodiments, a control is a historical control (i.e., of a test or assay performed previously, or an amount or result that is previously known). In some embodiments, a control is or comprises a printed or otherwise saved record. A control may be a positive control or a negative control.
[0049] Dosing regimen: A "dosing regimen", as that term is used herein, refers to a set of unit doses (at least one and often more than one) that are administered individually separated by periods of time. The recommended set of doses (i.e., amounts, timing, route of administration, etc.) for a particular therapeutic agent constitutes its dosing regimen.
[0050] Functional: As used herein, a "functional" biological molecule is a biological molecule in a form in which it exhibits a property and/or activity by which it is characterized.
[0051] Inhibition: As used herein, the terms "inhibition," "inhibit" and "inhibiting" refer to processes or methods of decreasing or reducing activity and/or expression of a protein or a gene of interest. Typically, inhibiting a protein or a gene refers to reducing expression or a relevant activity of the protein or gene by at least 10% or more, for example, 20%, 30%, 40%, or 50%, 60%, 70%, 80%, 90% or more, or a decrease in expression or the relevant activity of greater than 1-fold, 2-fold, 3-fold, 4-fold, 5-fold, 10-fold, 50-fold, 100-fold or more as measured by one or more methods described herein or recognized in the art.
[0052] In vitro: As used herein, the term "in vitro" refers to events that occur in an artificial environment, e.g., in a test tube or reaction vessel, in cell culture, etc., rather than within a multi-cellular organism.
[0053] In vivo: As used herein, the term "in vivo" refers to events that occur within a multi-cellular organism such as a non-human animal.
[0054] Isolated: As used herein, the term "isolated" refers to a substance and/or entity that has been (1) separated from at least some of the components with which it was associated when initially produced (whether in nature and/or in an experimental setting), and/or (2) produced, prepared, and/or manufactured by the hand of man. Isolated substances and/or entities may be separated from at least about 10%, about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, about 90%, about 95%, about 98%, about 99%, substantially 100%, or 100% of the other components with which they were initially associated. In some embodiments, isolated agents are more than about 80%, about 85%, about 90%, about 91%, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, about 99%, substantially 100%, or 100% pure. As used herein, a substance is "pure" if it is substantially free of other components. As used herein, the term "isolated cell" refers to a cell not contained in a multi-cellular organism.
[0055] Individual with MCL As used herein, "an individual with MCI (mild cognitive impairment)" is typically an individual who meets the following clinical criteria of amnestic MCI (Petersen et al. Arch Neural 56:303-308 (1999): 1) memory complaints corroborated by an informant, 2) objective memory impairment for age and education, 3) normal general cognitive function, 4) intact activities of daily living, and 5) the subject does not meet criteria for dementia.
[0056] Individual with EAD: As used herein, an "individual with EAD (early or moderate Alzheimer's disease)" is an individual who demonstrate the following criteria: 1) a decline in cognitive function for a previous higher level, 2) declines in one or more areas of cognition in addition to memory, 3) a clinical dementia rating scale score of 0.5 to 1, and 4) a clinical examination that excluded other causes of dementia.
[0057] Individual with LAD: As used herein, an "individual with LAD (severe or late stage Alzheimer's disease)" is an individual who meets the standard clinical diagnostic criteria for probable AD (McKhann et al. Neurology 34:939-48 (1984).
[0058] Reference value: As used herein, a "reference value" can be an absolute value; a relative value; a value that has an upper and/or lower limit; a range of values; an average value; a median value, a mean value, or a value as compared to a particular control or baseline value. A reference value can be based on an individual sample value, such as for example, a value obtained from a sample from the individual with AD, MCI or cognitive impairment, but at an earlier point in time, or a value obtained from a sample from an AD patient other than the individual being tested, or a "normal" individual, that is an individual not diagnosed with AD. The reference value can be based on a large number of samples, such as from AD patients or normal individuals or based on a pool of samples including or excluding the sample to be tested.
[0059] Neurological disease: As used herein, the phrase "neurological disease" refers to a disease or disorder of the central nervous system. Neurological diseases include multiple sclerosis, neuropathies, and neurodegenerative disorders such as AD, Parkinson's disease, amyotrophic lateral sclerosis (ALS), mild cognitive impairment (MCI) and frontotemporal dementia.
[0060] Normal individual: As used herein, a "Normal" individual or "healthy" individual refers to an individual who has or would be assessed by a physician as not having AD or MCI, and has an Mini-Mental State Examination (MMSE) (referenced in Folstein et al., J. Psychiatr. Res 1975; 12:1289-198) score or would achieve a MMSE score in the range of 25-30. A "Normal" individual is generally age-matched within a range of 5 to 10 years, including but not limited to an individual that is age-matched, with the individual to be assessed.
[0061] Protein: As used herein, the term "protein" refers to a polypeptide {i.e., a string of at least two amino acids linked to one another by peptide bonds). Proteins may include moieties other than amino acids {e.g., may be glycoproteins, proteoglycans, etc.) and/or may be otherwise processed or modified. Those of ordinary skill in the art will appreciate that a "protein" can be a complete polypeptide chain as produced by a cell (with or without a signal sequence), or can be a characteristic portion thereof. Those of ordinary skill will appreciate that a protein can sometimes include more than one polypeptide chain, for example linked by one or more disulfide bonds or associated by other means. Polypeptides may contain L-amino acids, D- amino acids, or both and may contain any of a variety of amino acid modifications or analogs known in the art. Useful modifications include, e.g., terminal acetylation, amidation, etc. In some embodiments, proteins may comprise natural amino acids, non-natural amino acids, synthetic amino acids, and combinations thereof. The term "peptide" is generally used to refer to a polypeptide having a length of less than about 100 amino acids. [0062] Subject: As used herein, the term "subject" or "patient" refers to any organism to which compositions in accordance with the invention may be administered, e.g. , for experimental, diagnostic, prophylactic, and/or therapeutic purposes. Typical subjects include animals (e.g., mammals such as mice, rats, rabbits, non-human primates, and humans; insects; worms; etc.).
[0063] Substantially: As used herein, the term "substantially" refers to the qualitative condition of exhibiting total or near-total extent or degree of a characteristic or property of interest. One of ordinary skill in the biological arts will understand that biological and chemical phenomena rarely, if ever, go to completion and/or proceed to completeness or achieve or avoid an absolute result. The term "substantially" is therefore used herein to capture the potential lack of completeness inherent in many biological and chemical phenomena.
[0064] Suffering from: An individual who is "suffering from" a disease, disorder, and/or condition has been diagnosed with or displays one or more symptoms of the disease, disorder, and/or condition.
[0065] Susceptible to: An individual who is "susceptible to" a disease, disorder, and/or condition has not been diagnosed with the disease, disorder, and/or condition. In some embodiments, an individual who is susceptible to a disease, disorder, and/or condition may not exhibit symptoms of the disease, disorder, and/or condition. In some embodiments, an individual who is susceptible to a disease, disorder, and/or condition will develop the disease, disorder, and/or condition. In some embodiments, an individual who is susceptible to a disease, disorder, and/or condition will not develop the disease, disorder, and/or condition.
[0066] Therapeutically effective amount: As used herein, the term "therapeutically effective amount" of a therapeutic agent means an amount that is sufficient, when administered to a subject suffering from or susceptible to a disease, disorder, and/or condition, to treat, diagnose, prevent, and/or delay the onset of the symptom(s) of the disease, disorder, and/or condition.
[0067] Therapeutic agent: As used herein, the phrase "therapeutic agent" refers to any agent that, when administered to a subject, has a therapeutic effect and/or elicits a desired biological and/or pharmacological effect. As used herein, the terms "therapeutic agent" and "agent" are used inter-changeably.
[0068] Treating: As used herein, the term "treat," "treatment," or "treating" refers to any method used to partially or completely alleviate, ameliorate, relieve, inhibit, prevent, delay onset of, reduce severity of and/or reduce incidence of one or more symptoms or features of a particular disease, disorder, and/or condition. Treatment may be administered to a subject who does not exhibit signs of a disease and/or exhibits only early signs of the disease for the purpose of decreasing the risk of developing pathology associated with the disease.
[0069] Definitions of specific functional groups and chemical terms are described in more detail below. For purposes of this invention, the chemical elements are identified in accordance with the Periodic Table of the Elements, CAS version, Handbook of Chemistry and Physics, 75th Ed., inside cover, and specific functional groups are generally defined as described therein. Additionally, general principles of organic chemistry, as well as specific functional moieties and reactivity, are described in Organic Chemistry, Thomas Sorrell, University Science Books, Sausalito, 1999; Smith and March March 's Advanced Organic Chemistry, 5th Edition, John Wiley & Sons, Inc., New York, 2001; Larock, Comprehensive Organic Transformations, VCH Publishers, Inc., New York, 1989; Carruthers, Some Modern Methods of Organic Synthesis, 3rd Edition, Cambridge University Press, Cambridge, 1987.
[0070] The compounds of the present invention may exist in particular geometric or stereoisomeric forms. The present invention contemplates all such compounds, including cis- and trans-isomers, R- and S-enantiomers, diastereomers, (D)-isomers, (L)-isomers, the racemic mixtures thereof, and other mixtures thereof, as falling within the scope of the invention.
[0071] Aliphatic: The term "aliphatic" or "aliphatic group", as used herein, denotes a hydrocarbon moiety that may be straight-chain (i.e., unbranched), branched, or cycloaliphatic (including fused, bridging, and spiro-fused polycyclic) and may be completely saturated or may contain one or more units of unsaturation, but which is not aromatic. Unless otherwise specified, aliphatic groups contain 1-6 carbon atoms. In some embodiments, aliphatic groups contain 1-4 carbon atoms, and in yet other embodiments aliphatic groups contain 1-3 carbon atoms. Suitable aliphatic groups include, but are not limited to, linear or branched, alkyl, alkenyl, and alkynyl groups, and hybrids thereof such as (cycloalkyl)alkyl, (cycloalkenyl)alkyl or (cycloalkyl)alkenyl.
[0072] Alkenyl: The term "alkenyl," as used herein, denotes a monovalent group derived from a straight- or branched-chain aliphatic moiety having at least one carbon-carbon double bond by the removal of a single hydrogen atom. In certain embodiments, alkenyl contains 2-6 carbon atoms. In certain embodiments, alkenyl contains 2-5 carbon atoms. In some embodiments, alkenyl contains 2-4 carbon atoms. In another embodiment, alkenyl contains 2-3 carbon atoms. Alkenyl groups include, for example, ethenyl ("vinyl"), propenyl ("allyl"), butenyl, l-methyl-2-buten-l-yl, and the like.
[0073] Alkyl: The term "alkyl," as used herein, refers to a monovalent saturated, straight- or branched-chain hydrocarbon radical derived from an aliphatic moiety containing between one and six carbon atoms by removal of a single hydrogen atom. In some embodiments, alkyl contains 1-5 carbon atoms. In another embodiment, alkyl contains 1-4 carbon atoms. In still other embodiments, alkyl contains 1-3 carbon atoms. In yet another embodiment, alkyl contains 1-2 carbons. Examples of alkyl radicals include, but are not limited to, methyl, ethyl, n-propyl, isopropyl, n-butyl, iso-butyl, sec-butyl, sec-pentyl, iso-pentyl, tert- butyl, n-pentyl, neopentyl, n-hexyl, sec-hexyl, n-heptyl, n-octyl, n-decyl, n-undecyl, dodecyl, and the like.
[0074] Alkynyl: The term "alkynyl," as used herein, refers to a monovalent group derived from a straight- or branched-chain aliphatic moiety having at least one carbon-carbon triple bond by the removal of a single hydrogen atom. In certain embodiments, alkynyl contains 2-6 carbon atoms. In certain embodiments, alkynyl contains 2-5 carbon atoms. In some embodiments, alkynyl contains 2-4 carbon atoms. In another embodiment, alkynyl contains 2-3 carbon atoms. Representative alkynyl groups include, but are not limited to, ethynyl, 2-propynyl ("propargyl"), 1-propynyl, and the like.
[0075] Amino: The term "amino," as used herein, refers to a group of the formula (-
NH2). [0076] Alkoxy: The term "alkoxy" refers to a "substituted hydroxyl" of the formula (-
OR1), wherein R1 is an alkyl group, as defined herein, and the oxygen moiety is directly attached to the parent molecule.
[0077] Alkylamino: The term "alkylamino" refers to a "substituted amino" of the formula (-NRh2), wherein Rh is, independently, a hydrogen or an alkyl group, as defined herein, and the nitrogen moiety is directly attached to the parent molecule.
[0078] Cycloaliphatic: The terms "cycloaliphatic", "carbocycle", "carbocyclyl",
"carbocyclo", or "carbocyclic", used alone or as part of a larger moiety, refer to a saturated or partially unsaturated cyclic aliphatic monocyclic or bicyclic ring systems, as described herein, having from 3 to 10 members, wherein the aliphatic ring system is optionally substituted as defined above and described herein. Cycloaliphatic groups include, without limitation, cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cycloheptyl, cycloheptenyl, cyclooctyl, cyclooctenyl, and cyclooctadienyl. In some embodiments, the cycloalkyl has 3-6 carbons. The terms "cycloaliphatic", "carbocycle", "carbocyclyl", "carbocyclo", or "carbocyclic" also include aliphatic rings that are fused to one or more aromatic or nonaromatic rings, such as decahydronaphthyl, tetrahydronaphthyl, decalin, or bicyclo[2.2.2]octane, where the radical or point of attachment is on an aliphatic ring.
[0079] Cyano: The term "cyano," as used herein, refers to a group of the formula (-CN).
[0080] Halogen: The terms "halo" and "halogen" as used herein refer to an atom selected from fluorine (fluoro, -F), chlorine (chloro, -Cl), bromine (bromo, -Br), and iodine (iodo, -I).
[0081] Nitro: The term "nitro," as used herein, refers to a group of the formula (-NO2).
[0082] Nitroso: The term "nitroso," as used herein, refers to a group of the formula (-
NO).
[0083] Partially unsaturated: As used herein, the term "partially unsaturated" refers to a ring moiety that includes at least one double or triple bond between ring atoms but is not aromatic. The term "partially unsaturated" is intended to encompass rings having multiple sites of unsaturation, but is not intended to include aryl or heteroaryl moieties, as herein defined.
[0084] Unsaturated: The term "unsaturated", as used herein, means that a moiety has one or more units of unsaturation.
DETAILED DESCRIPTION
[0085] The present invention provides, among other things, therapeutic compositions and methods that can effectively treat, slow or prevent mild cognitive impairment (MCI) or Alzheimer's disease (AD).
[0086] As described in the Examples section, the present invention is, in part, based on the following unexpected discoveries: (1) a protein complex PDS/TTR, known as a biomarker for early diagnosis of MCI or Alzheimer's disease, is neurotoxic and induces characteristic symptoms and features of Alzheimer's disease in cell cultures; (2) dihydropyridine calcium channel blockers (like nifedipine), their oxidized, nitroso derivatives and mixtures (which no longer function as calcium channel blockers), and/or T3/T4 effectively reduce or eliminate the ability of the PDS/TTR complex to induce AD-like symptoms and underlying enzymes and biochemical pathways in cell cultures and reduce endogenous levels of Aβ 1-40 peptide in animal models; and (3) human association studies demonstrated that the use of dihydropyridine calcium channel blockers significantly delays the onset of cognitive decline thus indicating that these compounds may be used to effectively treat Alzheimer's disease. More surprisingly, the inventors found that oxidized, nitroso nifedipine derivatives and mixtures no longer function as calcium channel blockers. Without wishing to be bound by any theory, it is contemplated that the ability of these compounds to treat MCI or Alzheimer's disease may be independent of their ability to block calcium channels.
[0087] Thus, the present invention contemplates methods and compositions that can effectively treat Alzheimer's disease based on therapeutically effective amount of nifedipine, oxidized or nitroso nifedipine derivatives, thyroxine (T4), triiodothyronine (T3) and combinations thereof. In some embodiments, the present invention provides methods for treating, slowing, or preventing Mild Cognitive Impairment (MCI) and/or Alzheimer's disease in a human subject, comprising administering to a subject who is suffering from or susceptible to MCI or Alzheimer's disease a therapeutically effective amount of an agent selected from the group consisting of nifedipine, oxidized nifedipine, nitroso-nifedipine, thyroxine (T4), triiodothyronine (T3) and combinations thereof, such that at least one symptom or feature associated with the MCI or Alzheimer's disease is reduced in abundance, intensity, severity, or frequency, or has delayed onset. In some embodiments, the agent suitable for the invention does not function as a calcium channel blocker.
[0088] It is further contemplated that inventive methods according to the invention can be combined with sensitive biomarkers and/or cognitive test scores to identify patents, including those at an early stage of the disease, for treatment and to monitor efficacy of the treatment. Thus, the present invention is particularly useful to treat early stage patients, especially, those patients having symptoms described as Mild Cognitive Impairment (MCI) and/or to prevent progression of MCI to Alzheimer's disease.
[0089] Various aspects of the invention are described in detail in the following sections.
The use of sections is not meant to limit the invention. Each section can apply to any aspect of the invention. In this application, the use of "or" means "and/or" unless stated otherwise.
Therapeutic Agents
[0090] Therapeutic agents suitable for the present invention include both calcium channel blockers (e.g., dihydropyridine calcium channel blockers such as nifedipine) and non-calcium channel blockers (e.g., oxidized nifedipine, nitroso-nifedipine, mixture of nifedipine and its derivatives, thyroxine (T4), triiodothyronine (T3)).
[0091] In some embodiments, a therapeutic agent suitable for the present invention is of formula (Ia) or (Ib):
Figure imgf000021_0001
(Ia) (Ib) or a pharmaceutically acceptable salt thereof, wherein: R1 and R2 are independently Ci_6 aliphatic or cyano; R3 and R4 are independently Ci_6 aliphatic;
R5 is halogen, Ci_6 aliphatic, hydroxyl, alkoxy, amino, alkylamino, cyano, nitro, or nitroso; and n is 0, 1, 2, or 3.
[0092] In some embodiments, compounds of formula (Ia) are referred to as "reduced" or
"dihydropyridines". In some embodiments, compounds of formula (Ib) are referred to as "oxidized" or "dehydro".
[0093] In some embodiments, R1 and R2 are independently Ci_3 alkyl. In some embodiments, R3 and R4 are independently Ci_4 alkyl. In some embodiments, R1 and R2 are methyl. In some embodiments, R3 and R4 are methyl.
[0094] In some embodiments, a therapeutic agent suitable for the present invention is nifedipine, oxidized nifedipine, or nitroso-nifedipine. As used herein, "nitroso-nifedipine" is an oxidized analog of nifedipine, as shown below.
Figure imgf000022_0001
nifedipine oxidized nifedipine nitroso-nifedipine
[0095] In some embodiments, therapeutic agents suitable for the present invention include, but are not limited to, dihyropyridine compounds such as amlodipine, aranidipine, azelnidipine, barnidipine, benidipine, cilnidipine, clevidipine, efonidipine, felodipine, isradipine, lacidipine, manidipine, lercanidipine, nicardipine, nifedipine, nilvadipine, nimodipine, nisoldipine, nitrendipine, and pranidipine. In some embodiments, therapeutic agents suitable for the present invention include, but are not limited to, oxidized amlodipine, oxidized aranidipine, oxidized azelnidipine, oxidized barnidipine, oxidized benidipine, oxidized cilnidipine, oxidized clevidipine, oxidized efonidipine, oxidized felodipine, oxidized isradipine, oxidized lacidipine, oxidized manidipine, oxidized lercanidipine, oxidized nicardipine, oxidized nifedipine, oxidized nilvadipine, oxidized nimodipine, oxidized nisoldipine, oxidized nitrendipine, and oxidized pranidipine. It will be understood by one of ordinary skill in the art that an "oxidized" dihydropyridine compound (e.g., oxidized amlodipine, oxidized nimodipine, oxidized nivaldipine) is the pyridine version of said compound.
Figure imgf000022_0002
nimodipine oxidized nimodipine
Figure imgf000023_0001
amlodipine oxidized amlodipine
Figure imgf000023_0002
nilvadipine oxidized nilvadipine
Further exemplary therapeutic agents include the following:
Figure imgf000023_0003
Figure imgf000023_0005
Figure imgf000023_0004
Figure imgf000024_0001
Figure imgf000025_0001
wherein Z is H, F, Cl, Br, or I;
Figure imgf000025_0002
wherein Z is H, F, Cl, Br, or I. [0097] In some embodiments, a therapeutic agent suitable for the present invention is of formula (II):
Figure imgf000026_0001
(H) or a pharmaceutically acceptable salt thereof, wherein: X is -CH2-, -O-, or -NH-; and Y is -H or -I.
[0098] In some embodiments, X is -CH2-. In some embodiments, X is -O-. In some embodiments, X is -NH-.
[0099] In some embodiments, a therapeutic agent suitable for the present invention is thyroxine (T4) or triiodothyronine (T3):
Figure imgf000027_0001
triiodothyronine (T3) thyroxine (T4)
[0100] In some embodiments, a therapeutic agent suitable for the present invention is a mixture of various compounds described herein. For example, two or more compounds of formula (Ia) or (Ib) can be combined to form a therapeutic agent. In some embodiments, two or more of nifedipine, oxidized nifedipine, and nitroso-nifedipine are combined. In some embodiments, T3 and/or T4 are combined with one or more of nifedipine, oxidized nifedipine, and nitroso-nifedipine. In certain embodiments, nifedipine, oxidized nifedipine, and nitroso- nifedipine are combined to form a nifedipine mix or mixture.
[0101] Compounds can be mixed at various mass or molar ratios. For example, a therapeutic agent according to the invention can be a mixture of two or more of nifedipine, oxidized nifedipine, nitroso-nifedipine, thyroxine (T4), and triiodothyronine (T3) at predetermined mass or molar ratios. In some embodiments, a therapeutic agent suitable for the invention contains a mixture of nitroso-nifedipine and nifedipine. In some embodiments, nitroso-nifedipine and nifedipine can be mixed at a mass or molar ratio of about 1000:1, about 500:1, about 200:1, about 100:1, about 64:1, about 32:1, about 16:1, about 10:1, about 8:1, about 5:1, about 4:1, about 3:1, about 2:1, about 1 :1, about 1 :2, about 1 :3, about 1 :4, about 1 :5, about 1 :8, about 1 :10, about 1 :16, about 1 :32, about 1 :64, about 1 :100, about 1 :200, about 1 :500, or about 1 : 1000. In some embodiments, nitroso-nefidipine and nifedipine can be mixed at a mass or molar ratio ranging from about 1 :1000 to about 1000:1 (e.g., about 1 :500 to about 500:1, about 1 :200 to about 200:1, about 1 : 100 to about 100:1, about 1 : 10 to about 10:1, about 1 : 16 to about 16:1, about 1:32 to about 32:1, about 1:64 to about 64:1, about 1:1 to about 32:1, about 1:1 to about 10:1, about 100:1 to about 1000:1, about 10:1 to about 100:1, about 1:1000 to 1:1, about 1:1 to about 1000:1, or about 1:100 to about 1:10). In some embodiments, a therapeutic agent suitable for the invention contains a mixture of oxidized-nifedipine and nifedipine. In some embodiments, oxidized-nifedipine and nifedipine can be mixed at a mass or molar ratio of about 1000:1, about 500:1, about 200:1, about 100:1, about 64:1, about 32:1, about 16:1, about 10:1, about 8:1, about 5:1, about 4:1, about 3:1, about 2:1, about 1:1, about 1:2, about 1:3, about 1:4, about 1:5, about 1:8, about 1:10, about 1:16, about 1:32, about 1:64, about 1:100, about 1:200, about 1 :500, or about 1 : 1000. In some embodiments, oxidized-nefidipine and nifedipine can be mixed at amass or molar ratio ranging from about 1:1000 to about 1000:1 (e.g., about 1:500 to about 500:1, about 1:200 to about 200:1, about 1:100 to about 100:1, about 1:10 to about 10:1, about 1:16 to about 16:1, about 1:32 to about 32:1, about 1:64 to about 64:1, about 1:1 to about 32:1, about 1:1 to about 10:1, about 100:1 to about 1000:1, about 10:1 to about 100:1, about 1:1000 to 1:1, about 1:1 to about 1000:1, or about 1:100 to about 1:10). In some embodiments, a therapeutic agent suitable for the invention contains a mixture of nitroso-nifedipine and oxidized nifedipine. In some embodiments, nitroso-nifedipine and oxidized-nifedipine can be mixed at a mass or molar ratio of about 1000:1, about 500:1, about 200:1, about 100:1, about 64:1, about 32:1, about 16:1, about 10:1, about 8:1, about 5:1, about 4:1, about 3:1, about 2:1, about 1:1, about 1:2, about 1:3, about 1:4, about 1:5, about 1:8, about 1:10, about 1:16, about 1:32, about 1:64, about 1:100, about 1:200, about 1:500, or about 1:1000. In some embodiments, nitroso- nefidipine and oxidized nifedipine can be mixed at a mass or molar ratio ranging from about 1:1000 to about 1000:1 (e.g., about 1:500 to about 500:1, about 1:200 to about 200:1, about 1:100 to about 100:1, about 1:10 to about 10:1, about 1:16 to about 16:1, about 1:32 to about 32:1, about 1:64 to about 64:1, about 1:1 to about 32:1, about 1:1 to about 10:1, about 100:1 to about 1000:1, about 10:1 to about 100:1, about 1:1000 to 1:1, about 1:1 to about 1000:1, or about 1 : 100 to about 1:10). In some embodiments, a therapeutic agent suitable for the invention contains a mixture of nitroso-nifedipine, oxidized nifedipine, and nifedipine. In some embodiments, nitroso-nifedipine, oxidized nifedipine, and nifedipine are mixed at a mass or molar ratio of about 5:1:3, 5:2:2, 6:3:1, 10:4:1, 3:1:5, 2:5:5, or 1:1:1. In some embodiments, a therapeutic agent contains a mixture of T3 and T4. In some embodiments, T3 and T4 can be mixed at a mass or molar ratio of about 1000:1, about 500:1, about 200:1, about 100:1, about 64:1, about 32:1, about 16:1, about 10:1, about 8:1, about 5:1, about 4:1, about 3:1, about 2:1, about 1 :1, about 1 :2, about 1 :3, about 1 :4, about 1:5, about 1 :8, about 1 : 10, about 1 :16, about 1 :32, about 1 :64, about 1 :100, about 1 :200, about 1 :500, or about 1 :1000. In some embodiments, T3 and T4 can be mixed at a mass or molar ratio ranging from about 1 : 1000 to about 1000: 1 (e.g., about 1 :500 to about 500:1, about 1 :200 to about 200:1, about 1 :100 to about 100:1, about 1 :10 to about 10:1, about 1 :16 to about 16:1, about 1 :32 to about 32:1, about 1 :64 to about 64:1, about 1 :1 to about 32:1, about 1 :1 to about 10:1, about 100:1 to about 1000:1, about 10:1 to about 100:1, about 1 :1000 to 1 :1, about 1 :1 to about 1000:1, or about 1 :100 to about 1 :10). In some embodiments, various compounds and mixtures described herein can be further combined to generate desirable therapeutic agents for the invention. For example, a T3/T4 mix can be combined with any of the nifedipine, nifedipine derivatives (e.g., oxidized or nitroso-nifedipine) or nifedipine mixtures described herein.
Biomarkers for Identifying Patients or Monitoring Treatment
[0102] Various biomarkers can be used to identify subject or patient who is suffering from, susceptible to or at risk of MCI or Alzheimer's disease. As used herein, a biomarker is a characteristic bio-molecule which is differentially present in a sample taken from a subject of one phenotypic status (e.g., having a disease) as compared with another phenotypic status (e.g., not having a disease). A biomarker is differentially present between different phenotypic statuses if the mean or median expression level of the biomarker in the different groups is calculated to be statistically significant. Biomarkers, alone or in combination, provide measures of relative risk that a subject belongs to one phenotypic status or another. Therefore, they are useful as markers for disease (diagnostics), therapeutic effectiveness of a drug (theranostics) and drug toxicity.
[0103] For example, the inventors have recently shown that levels of a ~55 kDa proteinaceous complex containing prostaglandin-D2-synthase and transthyretin (PDS/TTR complex) may serve as a sensitive and specific diagnostic biomarker of MCI and AD, as detailed in US Pat. Pub. No. 2008/0026405, which is incorporated herein by reference. [0104] Typically, the PDS/TTR complex presents in cerebrospinal fluid and appears to be a sensitive and specific biomarker of the disease. Formation of the PDS/TTR complex was been localized to the choroid plexus, an assembly of epithelial cells located adjacent to the lateral ventricles. The choroid plexus functions as the blood-CSF barrier. The choroid plexus passes water, salts and selected small molecules from the blood to the CSF but effectively prevents blood proteins form entering the CSF. Proteins required for CSF are synthesized by the choroid plexus. Thus, the choroid plexus also functions as the source of CSF. Epithelial cells isolated from choroid plexus obtained fresh from short post mortem autopsies of late stage AD patients have been grown and expanded in culture. Examination of cell culture medium obtained from AD epithelial cells showed elevated levels of the PDS/TTR complex compared to control cells. Thus, an elevated PDS/TTR complex level as compared to a normal control can be used to identify subjects or patients suffering from, susceptible to or at risk of developing MCI or Alzheimer's disease.
[0105] In some embodiments, a biomarker suitable for the present invention comprises at least one of transthyretin and/or a prostaglandin-H2 D-isomerase, and at least one second protein selected from tranthyretin, prostaglandin-H2 D-isomerase, beta-2-microglobulin, cystatin C, superoxide dismutase [Cu-Zn], plasma retinol-binding protein, phosphatidylethanolamine- binding protein, carbonic anhydrase 2 and/or serotransferrin. Mild cognitive impairment or Alzheimer's disease status is determined by correlating the obtained measurement with standards.
[0106] In some embodiments, neuronal thread protein, tau (total; T-tau and various phosphorylated forms; P-tau), and/or derivatives of amyloid precursor protein (APP) including Aβ4o and Aβ42, may be used as biomarkers to identify patient population for treatment with compositions and methods of the present invention. In some embodiments, a subject in need of treatment has an abnormal level of a protein biomarker complex as compared to a control, wherein the protein biomarker complex comprises one or more of (i) beta amyloid 40 (Aβ40), (ii) beta amyloid 42 (Aβ42), (iii) the ratio of Aβ40 to Aβ42, and (iv) the ratio of phosphorylated tau to total tau. [0107] Additional biomarkers have been reported in the literature and may be used to identify patients for treatment according to the invention including, but not limited to, those described in Fahnestock et al, J. Neural. Transm. Suppl. 2002(62) :241-52 (2002); Masliah et al, Neurobiol. Aging 16(4):549-56 (1995); Power et al, Dement. Geriatr. Cong. Disord. 12(2):167- 170 (2001); Burbach et al, J. Neurosci. 24(10):2421-30 (2004), Li et al, Neuroscience 113(3):607-15 (2002), and Sanna et al, J. Clin. Invest. 111(2):241-50 (2003), each of which is incorporated herein by reference.
[0108] In some embodiments, a biomarker is determined in a fluid sample obtained from the subject. In some embodiments, a fluid sample is selected from the group consisting of CSF, serum, whole blood, blood plasma, urine, ascitic fluid, saliva, tissue effusion, lavage, and combinations thereof.
[0109] Various methods can be used to measure biomarkers qualitatively and quantitatively. For example, to detect a protein complex (such as PDS/TTR), a sandwich enzyme linked immunoassay (ELISA) cane be utilized that traps a first component of the complex (e.g., PDS) and probes for a second component (e.g. TTR). Additional exemplary methods are described in US Pat. Pub. No. 2008/0026405, which is incorporated herein by reference. Other methods are well known in the art and can be used to practice the present invention.
[0110] Typically, the measured level of a biomarker is compared to one or more controls or reference levels. Suitable reference level used for comparison with the measured level for a AD biomarker may vary, depending on aspect of the invention being practiced, as will be understood by one of ordinary skill in the art. To identify subjects suffering from or susceptible to AD or MCI, a suitable "reference level" is typically a level indicative of healthy individuals, in particular, age-matched healthy individuals. A reference level can be determined in parallel with patient sample. A reference level can also be a pre-determined level or based on historical data. For example, a suitable reference level can be an average of levels obtained from a population that is not afflicted with AD or MCI. Typically, a suitable reference level is derived from (e.g., is the mean or median of) levels obtained from an age-matched population. [0111] Typically, a subject in need of treatment has an greater or elevated level of a biomarker described herein as compared to a control or reference level indicative of a healthy individual or population.
[0112] For treatment monitoring purposes, a suitable reference level is typically a level indicative of healthy individuals or individuals suffering from Alzheimer's disease (e.g., with a pre-determined stage, such as MCI, EAD, or LAD). A reference level can be determined in parallel with patient sample. A reference level can also be a pre-determined level or based on historical data. For example, a suitable reference level can be an average of levels obtained from a population that is not afflicted with AD or MCI, or a population that has been diagnosed with MCI or AD (e.g., EAD or LAD). Alternately, a suitable reference level may be a historical reference level for a particular patient, for example, a level that was obtained from a sample derived from the same individual, but at an earlier point in time (e.g., before the treatment or an earlier point in the treatment). Typically, a suitable reference level is derived from (e.g., is the mean or median of) levels obtained from an age-matched population.
[0113] For AD patient stratification (i.e., methods of stratifying AD patients into mild, moderate and severe stages of AD), suitable reference levels are normally derived from (e.g., is the mean or median of) levels obtained from a population which has been diagnosed with a particular stage of AD (e.g., EAD or LAD) or MCI.
[0114] In some embodiments, the level of a suitable biomarker (such as the ~55 kDa
PDS/TTR complex) can be used to monitor the efficacy of the treatment. Typically, the goal of a therapy would be, ideally, to decrease, lower or diminish the level of the PDS/TTR complex in a subject so that a fluid sample taken from the subject would contain no detectable complex. A more conservative, subsidiary, goal of therapy would be to forestall any increase in the level of the ~55 kDa PDS/TTR complex. Accordingly, a person of ordinary skill in the medical therapeutic arts would be able to determine whether a given therapeutic regime is accomplishing the chosen therapeutic goal based on the level of an appropriate biomarker. In this way, a person of ordinary skill in the medical therapeutic arts would also be able to determine the effective amount of a therapeutic agent described herein based on the measured level of a suitable biomarker as compared to appropriate controls or reference levels. [0115] Typically, aged-matched populations are used to derive various reference levels.
Age-matched populations are ideally the same age as the individual being tested, but approximately age-matched populations are also acceptable. Approximately age-matched populations may be within 1, 2, 3, 4, or 5 years of the age of the individual tested, or may be groups of different ages which encompass the age of the individual being tested. Approximately age-matched populations may be in 2, 3, 4, 5, 6, 7, 8, 9, or 10 year increments (e.g. a "5 year increment" group which serves as the source for reference values for a 62 year old individual might include 58-62 year old individuals, 59-63 year old individuals, 60-64 year old individuals, 61-65 year old individuals, or 62-66 year old individuals).
[0116] The process of comparing a measured value and a reference value can be carried out in any convenient manner appropriate to the type of measured value and reference value for the AD biomarker at issue. For example, "measuring" can be performed using quantitative or qualitative measurement techniques, and the mode of comparing a measured value and a reference value can vary depending on the measurement technology employed. For example, the measured values used in the methods of the invention will most commonly be quantitative values (e.g., quantitative measurements of concentration, such as nanograms of AD biomarker per milliliter of sample, or absolute amount). As with qualitative measurements, the comparison can be made by inspecting the numerical data, by inspecting representations of the data (e.g., inspecting graphical representations such as bar or line graphs). As a non- limiting example, a measured value is generally considered to be substantially equal to or greater than a reference value if it is at least about 95% of the value of the reference value (e.g., a measured value of 1.71 can be considered substantially equal to a reference value of 1.80). A measured value is considered less or lower than a reference value if the measured value is less than 95% of the reference value (e.g., a measured value of 1.7 can be considered less than a reference value of 1.80). Tests of cognitive function
[0117] Various cognitive tests may also be used to identify subject or patient who is suffering from, susceptible to or at risk of MCI or Alzheimer's disease. Two exemplary cognitive tests are the Mini Mental Status Examination (MMSE) and the Clinical Dementia Rating (CDR).
[0118] In some embodiments, an MMSE score is used to identify a subject in need of treatment with the compositions and methods described herein. An MMSE score is a composite score representing multiple tests of cognitive function. The maximum possible total MMSE score is 30 points. The MMSE can be used to classify the severity of cognitive impairment in patients with dementia or other medical conditions. Table 1 shows how MMSE scores generally represent degrees of cognitive function.
Table 1
Figure imgf000034_0001
[0119] In some embodiments, a subject in need of treatment has an MMSE score of 21-
26 (mild cognitive impairment), 11-20 (moderate cognitive impairment), or 0-10 (severe cognitive impairment).
[0120] In some embodiments, a CDR score is used to identify a subject in need of treatment with the compositions and methods described herein. An CDR score is constructed from six domains that are scored individually: memory, orientation, judgment and problem solving, community affairs, home and hobbies, and personal care. Table 2 shows how CDR scores generally represent degrees of cognitive function. Table 2
Figure imgf000035_0001
[0121] In some embodiments, a CDR score above 0 indicates that a subject may be suffering from, susceptible to or at risk of MCI or Alzheimer's disease. In some embodiments, a subject in need of treatment may have a CDR score of 0.5 (very mild dementia), 1 (mild dementia), 2 (moderate dementia), or 3 (severe dementia).
[0122] In some embodiments, a cognitive test score (such as an MMSE score or CDR score) can be used to monitor the efficacy of the treatment. Typically, an effective therapy should improve the cognitive test score. Therefore, by comparing the cognitive test scores before and after the treatment or from different time points of a treatment regimen, a person of ordinary skill in the medical therapeutic arts can determine whether a given therapeutic regime is effective. For example, a person of ordinary skill in the medical therapeutic arts would be able to determine or adjust the effective amount of a therapeutic agent described herein by based on relative cognitive test scores determined before the treatment or from different time points of a treatment regimen.
Pharmaceutical Compositions and Administration
[0123] The present invention encompasses pharmaceutical compositions comprising therapeutic agents such as those disclosed herein. In some embodiments, a pharmaceutical composition of the invention contain a therapeutically effective amount of a therapeutic agent and a pharmaceutically acceptable carrier. [0124] As used herein, the term "pharmaceutically acceptable carrier" means a non-toxic, inert solid, semi-solid liquid filler, diluent, encapsulating material, formulation auxiliary of any type, or simply a sterile aqueous medium, such as saline. Some examples of the materials that can serve as pharmaceutically acceptable carriers are sugars, such as lactose, glucose and sucrose, starches such as corn starch and potato starch, cellulose and its derivatives such as sodium carboxymethyl cellulose, ethyl cellulose and cellulose acetate; powdered tragacanth; malt, gelatin, talc; excipients such as cocoa butter and suppository waxes; oils such as peanut oil, cottonseed oil, safflower oil, sesame oil, olive oil, corn oil and soybean oil; glycols, such as propylene glycol, polyols such as glycerin, sorbitol, mannitol and polyethylene glycol; esters such as ethyl oleate and ethyl laurate, agar; buffering agents such as magnesium hydroxide and aluminum hydroxide; alginic acid; pyrogen-free water; isotonic saline, Ringer's solution; ethyl alcohol and phosphate buffer solutions, as well as other non-toxic compatible substances used in pharmaceutical formulations.
[0125] Wetting agents, emulsifϊers and lubricants such as sodium lauryl sulfate and magnesium stearate, as well as coloring agents, releasing agents, coating agents, sweetening, flavoring and perfuming agents, preservatives and antioxidants can also be present in the composition, according to the judgment of the formulator. Examples of pharmaceutically acceptable antioxidants include, but are not limited to, water soluble antioxidants such as ascorbic acid, cysteine hydrochloride, sodium bisulfite, sodium metabisulfϊte, sodium sulfite, and the like; oil soluble antioxidants, such as ascorbyl palmitate, butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), lecithin, propyl gallate, alpha-tocopherol and the like; and the metal chelating agents such as citric acid, ethylenediamine tetraacetic acid (EDTA), sorbitol, tartaric acid, phosphoric acid and the like.
[0126] The term "therapeutically effective amount" or simply "effective amount" of a therapeutic agent, as used herein, refers to an amount of therapeutic agent that is sufficient, when administered to a subject in need of treatment according to an appropriate regimen, to alleviate, ameliorate, stabilize, and/or delay the onset of at least one symptom or feature associated with MCI or Alzheimer's disease as well as delay in progression of one or more symptoms of MCI or Alzheimer's disease (e.g., delay in progression with respect to abundance, intensity, severity, or frequency). It will be understood, however, that the total daily usage of the therapeutic agents and compositions of the present invention will be decided by the attending physician within the scope of sound medical judgment. The specific therapeutically effective dose level for any particular patient will depend upon a variety of factors including the disorder being treated and the severity of the disorder; activity of the specific compound employed; the specific composition employed; the age, body weight, general health, sex and diet of the patient; the time of administration, route of administration, and rate of excretion of the specific compound employed; the duration of the treatment; drugs used in combination or coinciding with the specific compound employed; and like factors well known in the medical arts.
[0127] In some embodiments, a therapeutically effective dose of a therapeutic agent of the present invention can range, for example, from 0.01 to 25 mg/kg body weight or more usually from 0.1 to 15 mg/kg body weight. In some embodiments, a therapeutically effective amount of a therapeutic agent ranges from about 0.01 mg to about 2.5 g per dose (e.g., from about 0.01 mg to about 2.0 g, from about 0.01 mg to about 1.5 g, from about 0.01 mg to about 1.0 g, per dose). In some embodiments, a therapeutically effective amount of a therapeutic agent ranges from about 0.01 to about 1000 mg (e.g., about 0.01 to about 500 mg, about 0.01 to about 250 mg, about 0.01 to about 200 mg, about 0.01 to about 150 mg, about 0.01 to about 100 mg, about 0.01 to about 50 mg, about 0.01 to about 10 mg, about 0.01 to about 5 mg, about 0.01 to about 2.5 mg, about 0.01 to about 2.0 mg, about 0.01 to about 1.5 mg, about 0.01 to about 1.0 mg, about 0.01 to about 0.5 mg, about 0.01 to about 0.1 mg) per dose. In some embodiments, the therapeutically effective amount of a therapeutic agent (in particular, nitroso-nifedipine) ranges from about 100 mg to about 5 g (e.g., about 100 mg to about 3 g, about 100 mg to about 2.5 g, about 100 mg to about 2 g, about 100 mg to about 1.5 g, about 100 mg to about 1000 mg, about 100 mg to about 500 mg, about 100 mg to about 250 mg) per dose. In some embodiments, a therapeutically effective amount of a therapeutic agent can be about 0.01 mg, about 0.05 mg, about 0.1 mg, about 0.5 mg, about 1 mg, about 5 mg, about 10 mg, about 25 mg, about 50 mg, about 100 mg, about 500 mg, about 1000 mg, about 1.5 g, about 2 g, about 2.5 g, about 3 g, or about 5 g per dose. Typically, the amount described herein is the total amount of all active compounds in a composition. For example, if a composition contains a mix of nifedipine, nitroso-nifedipine and oxidized nifedipine, a therapeutically effective amount is the combined amount of nifedipine, nitroso-nifedipine and oxidized nifedipine.
[0128] In some embodiments, a therapeutic agent as described herein is administered once daily. In some embodiments, a therapeutic agent as described herein is administered multiple times per day, e.g., twice, three times, or four times daily. In some embodiments, a total daily dose of a therapeutic agent ranges from about 0.01 mg to about 5 g per day in multiple doses or in a single dose (e.g., from about 0.01 mg to about 4.0 g, from about 0.01 mg to about 3.0 g, from about 0.01 mg to about 2.5 g, from about 0.01 mg to about 2.0 g, from about 0.01 mg to about 1.5 g, from about 0.01 mg to about 1.0 g, per day in multiple doses or in a single dose). In some embodiments, a total daily dose of a therapeutic agent ranges from about 0.01 to about 1000 mg (e.g., about 0.01 to about 500 mg, about 0.01 to about 250 mg, about 0.01 to about 200 mg, about 0.01 to about 150 mg, about 0.01 to about 100 mg, about 0.01 to about 50 mg, about 0.01 to about 10 mg, about 0.01 to about 5 mg, about 0.01 to about 2.5 mg, about 0.01 to about 2.0 mg, about 0.01 to about 1.5 mg, about 0.01 to about 1.0 mg, about 0.01 to about 0.5 mg, about 0.01 to about 0.1 mg) per day in a single dose or in multiple doses. In some embodiments, a total daily dose of a therapeutic agent (in particular, nitroso-nifedipine) ranges from about 50 mg to about 5 g (e.g., about 50 mg to about 4 g, about 100 mg to about 3 g, about 100 mg to about 2.5 g, about 100 mg to about 2 g, about 100 mg to about 1.5 g, about 100 mg to about 1000 mg, about 100 mg to about 500 mg, about 100 mg to about 250 mg) per day in a single dose or in multiple doses. In some embodiments, a total daily dose of a therapeutic agent can be about 0.01 mg, about 0.05 mg, about 0.1 mg, about 0.5 mg, about 1 mg, about 5 mg, about 10 mg, about 25 mg, about 50 mg, about 100 mg, about 500 mg, about 1000 mg, about 1.5 g, about 2 g, about 2.5 g, about 3 g, about 3.5 g, about 4 g, about 4.5 g, or about 5 g. Typically, an amount described herein is the total amount of all active compounds in a composition. For example, if a composition contains a mix of nifedipine, nitroso-nifedipine and oxidized nifedipine, a therapeutically effective amount is the combined amount of nifedipine, nitroso-nifedipine and oxidized nifedipine. [0129] In some embodiments, a therapeutic agent as described herein is administered monthly, bi-weekly, weekly, twice a week, or three times a week. In these instances, the daily doses described above reflects the average daily dose.
[0130] In certain situations, it may be important to maintain a fairly high dose of the active agent in the blood stream of the patient, particularly early in the treatment. Hence, at least initially, it may be important to keep the dose relatively high and/or at a substantially constant level for a given period of time, e.g., at least about six or more hours, e.g., at least about twelve or more hour, e.g., at least about twenty-four or more hours.
[0131] The compounds of the present invention may be administered alone or in combination or in concurrent therapy with other agents which affect the central or peripheral nervous system, particularly selected areas of the brain.
[0132] Pharmaceutical compositions according to the present invention may be administered by any route, including oral, subcutaneous, intravenous, intraperitoneal, intramuscular, intracerebroventricular, intraparenchymal, intrathecal, intracranial, buccal, mucosal, nasal, rectal, auricular, conjunctival, cutaneous, electro-osmosis, endocervical, endosinusial, endotracheal, enteral, epidural, extra-amniotic, extracorporeal, hemodialysis, infiltration, interstitial, intra-abdominal, intra-amniotic, intra-arterial, intra-articular, intrabiliary, introbrochial, intrabursal, intracardiac, intracaritlaginous, intracavitary, intracerebral, intracisternal, intracorneal, intracoronal, intracoronary, intracorporus cavernosum, intradermal, intradiscal, intraductal, intraduodenal, intradural, intraepidermal, intraesophageal, intragastric, intragingival, intraileal, intralesional, intralymphatic, intramedullary, intrameningeal, intramuscular, intraocular, intraovarian, intrapericardial, intrapleural, intraprostatic, intrapulmonary, intrasinal, intrasynovial, intratendinous, intratesticular, intrathecal, intrathroacic, intratubular, intratumor, intratympanic, intrauterine, intravascular, intravenous bolus, intravenous drip, intraventricular, intravesical, intravitreal, iontophoresis, irrigation, laryngeal, nasogastric, occlusive dressing technique, ophthalmic, oropharyngeal, parenteral, percutaneous, peridural, perineural, periodontal, respiratory, retrobulbar, soft tissue, subarachnoid, subconjunctival, sublingual, submucosal, topical, transdermal, transmucosal, transplacental, transtracheal, transtympanic, ureteral, urethral, and vaginal. In certain embodiments, a pharmaceutical composition of the present invention is administered by a route selected from oral, subcutaneous, intravenous, transdermal, intraperitoneal, intramuscular, intracerebroventricular, intraparenchymal, intrathecal, intracranial, buccal, mucosal, nasal, and rectal. In certain embodiments, a pharmaceutical composition of the present invention is administered orally.
[0133] Liquid dosage forms for oral administration may include pharmaceutically acceptable emulsions, microemulsions, solutions, suspensions, syrups and elixirs containing inert diluents commonly used in the art, such as water, isotonic solutions, or saline. Such compositions may also comprise adjuvants, such as wetting agents; emulsifying and suspending agents; sweetening, flavoring and perfuming agents.
[0134] Injectable preparations, for example, sterile injectable aqueous or oleaginous suspensions may be formulated according to the known art using suitable dispersing or wetting agents and suspending agents. The sterile injectable preparation may also be a sterile injectable solution, suspension or emulsion in a nontoxic parenterally acceptable diluent or solvent, for example, as a solution in 1,3-butanediol. Among the acceptable vehicles and solvents that may be employed are water, Ringer's solution, U.S. P. and isotonic sodium chloride solution. In addition, sterile, fixed oils are conventionally employed as a solvent or suspending medium. For this purpose any bland fixed oil can be employed including synthetic mono- or diglycerides. In addition, fatty acids such as oleic acid are used in the preparation of injectables.
[0135] The injectable formulation can be sterilized, for example, by filtration through a bacteria-retaining filter, or by incorporating sterilizing agents in the form of sterile solid compositions, which can be dissolved or dispersed in sterile water or other sterile injectable medium just prior to use.
[0136] In order to prolong the effect of a drug, it is often desirable to slow the absorption of a drug from subcutaneous or intramuscular injection. The most common way to accomplish this is to inject a suspension of crystalline or amorphous material with poor water solubility. The rate of absorption of the drug becomes dependent on the rate of dissolution of the drug, which is, in turn, dependent on the physical state of the drug, for example, the crystal size and the crystalline form. Another approach to delaying absorption of a drug is to administer the drug as a solution or suspension in oil. Injectable depot forms can also be made by forming microcapsule matrices of drugs and biodegradable polymers, such as polylactide-polyglycoside. Depending on the ratio of drug to polymer and the composition of the polymer, the rate of drug release can be controlled. Examples of other biodegradable polymers include polyorthoesters and polyanhydrides. Depot injectables can also be made by entrapping the drug in liposomes or microemulsions, which are compatible with body tissues.
[0137] Suppositories for rectal administration of the drug can be prepared by mixing the drug with a suitable non-irritating excipient, such as cocoa butter and polyethylene glycol which are solid at ordinary temperature but liquid at the rectal temperature and will, therefore, melt in the rectum and release the drug.
[0138] Solid dosage forms for oral administration include, but are not limited to, capsules, tablets, pills, powders, gelcaps and granules. In such solid dosage forms, therapeutic agent may be admixed with at least one inert diluent such as sucrose, lactose or starch. Such dosage forms may also comprise additional substances other than inert diluents, e.g., tableting lubricants and other tableting aids such as magnesium stearate and microcrystalline cellulose. In the case of capsules, tablets and pills, the dosage forms may also comprise buffering agents. Tablets and pills can additionally be prepared with enteric coatings and other release-controlling coatings.
[0139] Solid compositions of a similar type may also be employed as fillers in soft and hard- filled gelatin capsules using such excipients as lactose or milk sugar as well as high molecular weight polyethylene glycols and the like.
[0140] The active compounds can also be in micro-encapsulated form with one or more excipients as noted above. The solid dosage forms of tablets, dragees, capsules, pills, and granules can be prepared with coatings and shells such as enteric coatings and other coatings well known in the pharmaceutical formulating art. They may optionally contain opacifying agents and can also be of a composition that they release the active ingredient(s) only, or preferably, in a certain part of the intestinal tract, optionally in a delayed manner. Examples of embedding compositions which can be used include polymeric substances and waxes. [0141] Dosage forms for topical or transdermal administration of a compound of this invention further include ointments, pastes, creams, lotions, gels, powders, solutions, sprays, inhalants or patches. The active component is admixed under sterile conditions with a pharmaceutically acceptable carrier and any needed preservatives or buffers as may be required. Ophthalmic formulations, ear drops, eye ointments, powders and solutions are also contemplated as being within the scope of this invention.
[0142] The ointments, pastes, creams and gels may contain, in addition to an active compound of this invention, excipients such as animal and vegetable fats, oils, waxes, paraffins, starch, tragacanth, cellulose derivatives, polyethylene glycols, silicones, bentonites, silicic acid, talc and zinc oxide, or mixtures thereof.
[0143] Powders and sprays can contain, in addition to the active compounds of this invention, excipients such as lactose, talc, silicic acid, aluminum hydroxide, calcium silicates and polyamide powder, or mixtures of these substances. Sprays can additionally contain customary propellants, such as chlorofluorohydrocarbons.
[0144] Transdermal patches can provide controlled delivery of active compound to the body. Such dosage forms can be made by dissolving or dispersing the compound in the proper medium. Absorption enhancers can also be used to increase the flux of the compound across the skin. The rate can be controlled by either providing a rate controlling membrane or by dispersing the compound in a polymer matrix or gel.
[0145] Pharmaceutical compositions described herein can be formulated for immediate release or controlled release (also referred to as slow, sustained or extended release). Various slow or extended release formulations or devices are well known to those of ordinary skill in the art. Examples include, but are not limited to, those described in U.S. Pat. Nos. 5,674,533, 5,059,595, 5,120,548, 5,073,543, 5,639,476, 5,354,556, and 5,733,566, each of which is incorporated herein by reference. Such dosage forms can be used to provide slow or controlled- release of one or more active ingredients using, for example, hydropropylmethyl cellulose, other polymer matrices, gels, permeable membranes, osmotic systems, multilayer coatings, microparticles, liposomes, microspheres, or a combination thereof to provide the desired release profile in varying proportions. Suitable controlled-release formulations known to those of ordinary skill in the art can be readily selected and adapted for use with therapeutic agents of the invention. For example, the invention encompasses solid oral dosage forms such as, but not limited to, tablets, capsules, gelcaps, and caplets that are formulated for controlled-release (i.e., slow release, extended release, or sustained release).
[0146] Advantages of controlled-release formulations include extended activity of the drug, reduced dosage frequency, and increased patient compliance. For example, controlled or extended release formulations can keep adequate dose levels constantly available inside a patient body to enhance delivery across the blood-brain barrier.
[0147] Most controlled-release formulations are designed to initially release an amount of therapeutic agent (active ingredient) that promptly produces the desired therapeutic effect, and gradually and continually release of other amounts of thug to maintain this level of therapeutic or prophylactic effect over an extended period of time. In order to maintain this constant level of drug inside the body, the drug must be released from the dosage form at a rate that will replace the amount of drug being metabolized and excreted from the body. Controlled-release of an active ingredient can be stimulated by various conditions including, but not limited to, pH, temperature, enzymes, water, or other physiological conditions or compounds.
[0148] In some embodiments, two or more therapeutic agents may be administered in combination. The two or more therapeutic agents may be administered separately from one another, as part of a multiple dosage regimen. Alternatively, those agents may be part of a single dosage form, mixed together with a compound of this invention in a single composition. If administered as part of a multiple dosage regime, the two therapeutic agents may be submitted simultaneously, sequentially or within a period of time from one another normally within five hours from one another.
[0149] As used herein, the term "combination," "combined," and related terms refers to the simultaneous or sequential administration of therapeutic agents in accordance with this invention. For example, a compound of the present invention may be administered with another therapeutic agent simultaneously or sequentially in separate unit dosage forms or together in a single unit dosage form. Accordingly, the present invention provides a single unit dosage form comprising a provided compound, an additional therapeutic agent, and a pharmaceutically acceptable carrier, adjuvant, or vehicle.
[0150] The invention is provided in numerous embodiments and can be discerned, inter alia, in various examples. The following examples provide an illustrative but non-limiting description of the breadth and applicability of the invention.
EXAMPLES
Example 1. Neurotoxic effect of PDS/TTR complex
[0151] It has been shown that examination of cell culture medium obtained from epithelial cells derived from Alzheimer's disease patients showed elevated levels of the PDS/TTR complex compared to control cells, indicating that the PDS/TTR complex can be used as an effective biomarker for the early diagnosis of Alzheimer's disease. See, U.S. Application Pub. No. 20080026405, the disclosure of which is incorporated by reference herein. This example shows that in addition to being a biomarker for disease, the PDS/TTR complex is also neurotoxic.
[0152] First of all, it was found that acrolein (an alpha, beta unsaturated three carbon aldehydic by-product of lipid peroxidation) causes normal control epithelial cells to express the PDS/TTR complex into culture medium at comparable levels to the epithelial cells derived from Alzheimer's disease patients. For these experiments, primary cultures of choroid plexus epithelail cells were established from short post mortem interval autopsies using established methods. AD and normal control cultures were grown to confluence in MEM growth medium containing 2% fetal bovine serum and 1% epithelial growth factor (EGF). Normal control cultures were switched to Opti-MEM containing N2 supplement and were treated with vehicle (controls) or with 5 μM acrolein for 72 hours. Cultures from AD subjects were switched to N2 supplemented medium and maintained for 72 hours. After treatment, medium was collected from each flask and was desalted using PD-10 columns. The eluted proteins were then freeze- dried, resuspended in 25 μl water and analyzed using Western blot analysis and antibodies specific to PDS and TTR. Figure 1 shows exemplary results illustrating an Western blot analysis of the PDS/TTR complex expressed in cell culture medium by control epithelial cells, control epithelial cells treated with acrolein, and epithelial cells derived from late stage Alzheimer's disease patients. As shown in Figure 1, acrolein increased the expression of the PDS/TTR complex in control epithelial cells to a level comparable to that in late stage AD (LAD) epithelial cells.
[0153] Medium from LAD epithelial cells that contains the PDS/TTR complex was then used to treat cortical neurons. To determine if PDS/TTR complex generated by LAD choroid plexus epithelial cultures or normal control cultures treated with vehicle or with 5 μM acrolein negatively impacted primary cortical neurons, normal control epithelial cultures were switched to N2 supplemented medium and treated with vehicle alone (controls) or with 5 μM acrolein for 16 hours. LAD cultures were switched to N2 medium for 16 hours. After treatment, medium was collected from each culture type (LAD; normal controls treated with vehicle alone or normal controls treated with 5μM acrolein) and was added to primary rat neuron cultures (7 days in culture). Primary cultures treated were subjected to the conditioned medium for 16 hours and cell viability was measured using MTT reduction assays. An exemplary result was shown in Figure 2. As shown in Figure 2, the survival rate for cortical neurons treated with LAD epithelial medium is significantly lower as compared to the control (Figure 2). This experiment indicates that the PDS/TTR complex is itself neurotoxic.
[0154] To further investigate the neurotoxic effect of the PDS/TTR complex, SY5Y neuroblastoma cells were exposed to conditioned medium from LAD or normal control epithelial cells for 16 hours. Following exposure to conditioned medium, cells were fixed in 70% methanol/30% acetone and were subjected to immunohistochemistry using anti-PHF-1 antibody. PHF-I recognizes aberrantly phosphorylated Tau as observed in AD NFT (neurofibrillary tangles). As shown in Figure 3, close to 25% of SY5Y cells treated with LAD epithelial cell medium are PHF-I positive as compared to about 3% of SY5Y cells treated with control medium. Paired helical filaments are precursors to neurofibrillary tangles. Therefore, PHFl immunopositivity is typically an indicator of the formation of late-stage neurofibrillary tangles in Alzheimer's disease. Thus, this experiment shows that the PDS/TTR complex promotes the formation of paired helical filaments in SY5Y neuroblastoma cells, indicating the PDS/TTR that complex can promote amyloid beta peptide (AB) generation by H4 neuroglioma cells.
[0155] To determine if the complex generated by epithelial cultures would impact inflammatory cytokine pathways, cultures of human astrocytomas were plated at a density of 2.5 X lO5 cells/well and were exposed to conditioned medium for 24 hours. Following exposure medium was collected from each well and levels of inflammatory cytokines (IL-6, TNF-α, TGF- β and IL-6) were determined using commercially available ELISAs. Results of the assays showed the PDS/TTR complex activated 2 inflammatory cytokine pathways (i.e., IL-6, TNF-α) in astrocytoma cultures (data not shown), indicating a role of the PDS/TTR in neuroinflammation.
[0156] In summary, the experiments described in this example established that the
PDS/TTR complex causes various biochemical changes that can directly impact hallmarks of Alzheimer's disease.
Example 2. Nifedipine, Nifedipine analog mix and/or T3/T4 inhibit PDS/TTR expression
[0157] The assays described in Example 1 provide a tool to identify potential therapeutic agents that can protect neuronal cells against the PDS/TTR complex. The inventors observed that compounds such as nifedipine (l,4-dihydro-2,6-dimethyl-4-(2-nitrophenyl)-3,5- pyridinydicarboxylic acid dimethyl ester, CAS#21829-25-4 (Sigma Aldrich)), a calcium channel blocker prescribed for high blood pressure; or nifedipine analogs such as oxidized derivative of nifedipine ((2,6-dimethyl-4-(2-nitrophenyl)- 3,5-pyridinedicarboxylic acid dimethyl ester, CAS# 67035-22-7 (Sigma Aldrich)) or a nitroso derivative of nifedipine (2,6-dimethyl-4-(2- nitrosophenyl)- 3,5-pyridinedicarboxylic acid dimethyl ester, CAS#50428-14-3 (Sigma Aldrich)), can effectively inhibit the expression of PDS/TTR complex in cell culture, individually or in combination. In addition, T3 and T4 were also evaluated and found to be effective in inhibiting the expression of PDS/TTR complex. [0158] Specifically, epithelial cells were treated with 5 μM acrolein, 5 μM acrolein plus
0.5 μM T3/ 0.5 μM T4, 5 μM acrolein plus 1 μM nifedipine mixture (nitroso-nifedipine 55%, oxidized nifedipine 11% and nifedipine 34%), or 5 μM acrolein plus 1 μM nifedipine mixture and 0.5 μM T3/ 0.5 μM T4, as described in Example 1. The amount of PDS/TTR secreted into the culture medium by each culture was determined by Western blot analysis as described above. Exemplary data was shown in Figure 4. As can be seen, the amount expressed by cells treated with acrolein plus T3/T4, acrolein plus nifedipine mixture, or acrolein plus nifedipine mixture and T3/T4, was significantly less than that expressed by cells treated only with acrolein.
[0159] In addition, immunostaining was used to determine the PDS/TTR-positive cells and the numbers of PDS/TTR-positive cells from treated and untreated cell cultures were counted and compared. Exemplary results were summarized in Figure 5. As can be seen from Figure 5, the number of PDS/TTR-positive cells in acrolein alone-treat sample is about 600% of the number of PDS/TTR-positive cells in untreated control. By contrast, the numbers of PDS/TTR-positive cells in samples treated with acroline plus acrolein plus T3/T4, acrolein plus nifedipine mixture, or acrolein plus nifedipine mixture and T3/T4 were significantly reduced as compared to untreated control.
[0160] To determine if the nifedipine mix functions through blocking calcium channels, we evaluated the impact of the nifedipine mix on the calcium channels. SY5Y neuroblastoma cultures were pretreated for 16 hours with fresh nifedipine or the nifedipine mix and were then switched to calcium free medium and loaded with 5 μM Fura-2 fluorescent dye. Cultures were then rinsed with calcium free medium and exposed to calcium containing medium and fluorescence resulting from Ca binding to Fura-2 was measured using confocal microscopy and excitation at 340 nm. 50 to 100 cells were imaged per dish for 3 separate dishes. An exemplary result is shown in Figure 6. Interestingly, as shown in Figure 6, the nifedipine mix had minimal (-30% ) activity as a calcium channel blocker compared to fresh nifedipine indicating these compounds may act through an alternative, novel mechanism.
[0161] Therefore, the experiments described in this example indicate that nifedipine analog mix and T3/T4, alone or in combination, can effectively inhibit PDS/TTR expression in epithelial cells, and this effect is likely to be independent of calcium channels. Furthermore, T3/T4 improved the effectiveness of the nifedipine analogs.
Example 3. Nifedipine analogs inhibit inflammatory cytokine production
[0162] It was reported that inflammatory response elements (cytokines) are elevated in
Alzheimer's disease patients. The inventors tested the nifedipine mix and individual analogs in astrocytoma cultures. Human astrocytoama cells were plated at 2.5 X lO5 cells/well in 6 well culture plates and were grown for 24 hours. Cultures were then switched to serum free Opti- MEM and treated with the nifedipine mixture and individual analogs for 24 hours. Three 6-well plates were subjected to each treatment. Following treatment, medium was collected from each well and levels of IL-IB, IL-6, TNF-α and TGF-B were measured using commercially available ELISAs. Exemplary results are shown in Figure 7. As can be seen from Figure 7, IL-I, IL-6 and TNF-α secreted in the medium were significantly reduced with the treatment of nifedipine mix or oxidized nifedipine, indicating these compounds have a direct positive effect on neuroinflammation.
Example 4. Nifedipine, Nifedipine mix and/or T3/T4 reduce PHF-I levels
[0163] As described in Example 1, SY5Y neuroblastoma cells exposed to medium from
LAD epithelial cells that contained significantly higher levels of the PDS/TTR complex displayed significantly increased PHF-I immunostaining as compared to those exposed to medium from untreated control cultures. In this experiment, SY5Y cells were exposed to medium from epithelial cells treated with acrolein and combinations of nifedipine, nifedipine analogs, mixtures of nifedipine analogs and T3/T4 using procedures described in Example 1. As shown in Figure 8, nifedipine mix and nifedipine/nifedipine analogs plus T3/T4 significantly reduced PHF-I levels. Example 5. Inhibition of Aβ 1-42 production from H4 neuroglioblastoma cells
[0164] In this example, the inventors used H4 neuroglioblastoma cells stably transfected to overexpress amyloid precursor protein (APP) to further investigate if nifedipine, nifedipine analogs (e.g., oxidized nifedipine or nitroso-nifedipine) and/or T3/T4 can inhibit the production of Aβ 1-42. H4 neuroglioblastoma cells stably transfected with a construct overexpressing amyloid precursor protein (APP) secret ABi_42 into the culture medium. These H4 cells were treated with 1 μM fresh nifedipine, 1 μM oxidized nifedipine, 1 μM nitroso-nifedipine, or 0.5 μM T3/0.5 μM T4 for 16 hours. The AB levels in the culture medium were measured using ELISAs (Invitrogen). As shown in Figure 9, treatment of fresh nifedipine, oxidized nifedipine, nitroso- nifedipine, or T3/T4 lead to significantly decreased production of AB 1-42.
[0165] Furthermore, the effect of nifedipine, nifedipine analogs and nifedipine mix on
AB 1-42 production from H4 cells were further tested with and without T3/T4. Exemplary results are summarized in Figure 10. As can be seen, T3/T4 improves the inhibitory effect of nifedipine, nifedipine analogs and nifedipine mix on AB 1-42 production.
[0166] We then tested if other calcium channel blockers can inhibit Aβ 1-42 generation in H4 neuroglioma cultures. Known calcium channel blockers such as Amilodpine, Dilitiazem, Felodipine, Isradipine, Nicardipine, and Nimodipine were used in this experiment. Specifically, H4 cells were treated with 1 μM each drug, with and without T3/T4, in opti-MEM (Serum free) for 16 hours and AB 1-42 secreted into medium was measured using Invitrogen ELISAs. Exemplary results are shown in Figure 11. As shown in Figure 11 , Nicardipine, showed a trend (p < 0.10) toward a significant decrease in AB secretion and Nimodipine led to a significant (p < 0.05) decrease in AB formation. The other drugs did not significantly alter levels of AB formation. Combining the alternate calcium channel blockers with T3/T4 showed a significant decrease of AB formation when T3/T4 were combined with Amlodipine and Dilitiazem. Combinations of T3/T4 with the other drugs did not provide any significant decrease in AB formation. Example 6. Inhibition of beta secretase (BACE) and gamma secretase activity
[0167] This surprising finding that nifedipine, nifedipine analogs and nifedipine mix can effectively inhibit Aβi_42 peptide generation prompted further investigation into possible mechanism of Aβi_42 peptide reduction. It was contemplated that Aβi_42 production depends on the activity of beta secretase (BACE), an enzyme that cleaves the amyloid precursor protein at the beta secretase cleavage site, and the gamma secretase complex composed of presenilin-1 (PS- 1), nicastrin, APH-I and PEN-2 that cleaves at the gamma secretase cleavage site. The inventors tested whether the inhibition of Aβi_42 production in our culture model system was due to inhibition of BACE and/or gamma secretase activities.
[0168] BACE activity was measured using a fluorescent substrate and purified recombinant BACE as part of a commercial kit from Invitrogen. As shown in Figure 12, nifedipine alone or in combination with thyroxine slightly inhibited BACE activity; however, nitroso-nifedipine alone and in combination with thyroxine led to significant inhibition of BACE activity (Figure 12).
[0169] Examination of protein levels of BACE and individual components of the gamma secretase complex in H4 cultures treated with the nifedipine mix alone or in combination with T3/T4 revealed that the nifedipine mix alone significantly reduced levels of PS-I and PEN-2. Levels of BACE-I were decreased but not significantly. However, the nifedipine mix plus T3/T4 significantly reduced PS-I, PEN-2, BACE-I and Nicastrin. APH-I was not affected by any treatment. Exemplary results were shown in Figure 13. Protein levels were determined in individual cells (50 -100 cells/dish; 3 dishes/experiment) using immunohistochemistry and confocal microscopy and were verified in total cell homogenate using Western blot analysis. Antibodies specific to each protein were purchased from commercial vendors.
[0170] Experiments described in this example demonstrated that nifedipine mixtures, their oxidized and nitroso derivatives, and/or T3/T4 directly act on the enzymes responsible for AB production. Example 7. Inhibition of Aβ 1-40 production in vivo
[0171] Based on the in vitro data described above, the inventors initiated an acute exposure study in 3 month old C57-Black-6 (C57BL/6) mice. In this study, six groups of six C57BL/6 mice were subjected to intraperitoneal (IP) injections of vehicle (2%DMSO/98% polyethylene glycol-3000 (PEG-3000), 25 mg/kg nifedipine or nifedipine mix, T3/T4 (10 mg/kg T3 and 10 mg/kg T4), nifedipine mix plus T3/T4 and nifedipine plus T3/T4 on three consecutive days. Animals were euthanatized 1 hour after the third injection. The brains and terminal serum were removed and immediately frozen in liquid nitrogen and stored at -80 0C until used for analysis.
[0172] One hemisphere of brains was homogenized for AB 1-40 measurements
(Invitrogen ELISA) and the other homogenized for protein levels. In addition, levels of PS-I, BACE, cleaved Notch, an essential substrate for PS-I, Nicast, APH-I were measured using Western blot analysis. As shown in Figure 14, mice treated with both T3/T4 and nifedipine mix plus T3/T4 showed a modest (25%) but significant decrease in Aβ i_40 levels compared to animals treated with vehicle. Levels of PS-I, Nicast, and APH-I were significantly decreased in mice treated with nifedipine, nifedipine mix plus T3/T4. BACE protein levels were significantly decreased in mice treated with nifedipine, nifedipine plus T3/T4 and T3/T4 alone. In contrast, there were no significant differences in levels of cleaved Notch with any treatment (Figure 14).
[0173] Additionally the brains were extracted and analyzed by GC/MS for levels of nifedipine and its analogs. Oxidized nifedipine was found in all samples analyzed indicating that components of the mixture were passing the blood-brain barrier and thus available for neuronal protection. This experiments has shown that these derivatives possess the brain permeability desired for treatment of Alzheimer's disease.
[0174] Experiments described in this example demonstrated that nifedipine mixtures, their oxidized and nitroso derivatives, and/or T3/T4 reduce endogenous levels of Aβ 1-40 peptide in vivo. Example 8. Inhibition of Orphan G-coupled receptor protein 3 (GPCR-3) in vitro and in vivo
[0175] This example was conducted to test if nifedipine, nifedipine mixtures, and/or
T3/T4 can inhibit the orphan G-coupled receptor protein 3 (GPCR-3), an enzyme which is suggested to play a role in maintaining stability of the gamma secretase complex (which, as discussed above, is important for cleavage of APP to form Aβ).
[0176] H4 neuroglioblastoma cells were treated with 1 μM mixed nifedipine, 1 μM mixed nifedipine plus 0.5 μM T3/0.5 μM T4, 0.5 μM T3/0.5 μM T4, 1 μM fresh nifedipine, 1 μM fresh nifedipine plus 0.5 μM T3/0.5 μM T4 for 16 hours. Levels of GPCR-3 were measured using Western blot analysis using a GPCR-3 specific antibody. As shown in Figure 15, nifedipine mixtures, fresh nifedipine, and/or T3/T4 significantly reduced GPCR-3 expression levels in H4 cells.
[0177] In addition, GPCR-3 levels were determined in the C57BL/6 mice described above in Example 7 using Western blot analysis. Exemplary results are also shown in Figure 15. Nifedipine mixtures and T3/T4, fresh nifedipine, and T3/T4 also reduced GPCR-3 expression levels in mice.
[0178] Therefore, this example demonstrated that nifedipine mixtures, their oxidized and nitroso derivatives, and/or T3/T4 reduce GPCR-3 levels in vitro and in vivo.
[0179] To determine if the reduction of GPCR-3 levels by nifedipine mixtures, their oxidized and nitroso derivatives, and/or T3/T4 is through a pathway involved in blood pressure regulation, we tested known blood pressure drugs such as atenolol, captopril, and enantopirl on H4 cells. Specifically, H4 cells were treated with 1 μM each drug, with and without T3/T4, in Opti-MEM (Serum free) medium for 16 hours and levels of GPCR-3 were measured using confocal microscopy and a specific anti-GPCR-3 antibody. Exemplary results are shown in Figure 15 a. As shown in Figure 15 a, only captopril + T3/T4 led to a significant change (decrease) in levels of GPCR-3. This experiment indicates that the reduction of GPCR-3 by nifedipine mixtures, their oxidized and nitroso derivatives, and/or T3/T4 is independent of blood pressure pathways. Example 9. Inhibition of Tau Phosphorylation
[0180] In this example, we tested if nifedipine, nifedipine mixtures, their oxidized and nitroso derivatives, and/or T3/T4 can reduce phosphorylated Tau protein. Phosphorylated tau protein can result in the self-assembly of tangles of paired helical filaments and straight filaments, which are involved in the pathogenesis of Alzheimer's disease.
[0181] Although there are multiple kinases involved in Tau phosphorylation, glycogen synthase kinase-3B (GSK-3β) has received considerable attention as a major contributor to Tau hyperphosphorylation in AD. GSK-3β is present in -95% paired helical filaments identified using specifϊc-phospho-Tau antibodies. GSK-3β, a constitutively active kinase is inactivated by phosphorylation of Ser 9 by protein kinase B (Akt). Akt, a serine/threonine kinase is regulated by phosphatidylinositol kinase (PI3K) mediated signaling and is activated by phosphorylation of a regulatory threonine residue (Thr-308) by phosphatidylinositol dependent kinase 1 (PDKl) and by phosphorylation of Ser 473 by PDKα/TORC2 kinase. In addition, activation of the Akt/GSK- 3β pathway may be mediated by GCPRs coupled to Gαl2/13 heterotrimeric G proteins. Activation of Gαi2 has been shown to stimulate RhoA and its effector Rho kinase (ROCK). ROCK phosphorylated at ser 160 further transactivates a receptor tyrosine kinase (RTK) that activates the PI3K signaling pathway leading to phosphorylation/activation of Akt/GSK-3β (reviewed by New et al, "G protein-coupled receptor-induced Akt activity in cellular proliferation and apoptosis," FEBSJ, 2007; 274:6025-36.). Phosphoryalted Akt increases phosphorylation and inactivation of GSK-3β therefore reducing Tau phosphorylation.
[0182] We examined levels and the phosphorylation status of proteins involved in the tau phorphorylation pathway described above in the mouse brains treated with nifedipine, nifedipine mix and/or T3/T4 as described in Example 7. As shown in Figure 16, the levels of phosphoryalted ROCK (p-ROCK) and GSK-3β (p-GSK-3β) were significantly increased in mice treated with nifedipine or nifedipine mix plus T3/T4. T3/T4 alone also significantly increased the level of p-GSK-3β. The total protein levels of ROCK were not affected by any of the treatment. The level of p-25 was slightly reduced in treated mice. These results indicate that nifedipine, nifedipine mix and/or T3/T4 treatment can lead to reduced Tau phosphorylation in vivo. Example 10. Human association studies
[0183] Human association studies were conducted to determine the impact of calcium channel blockers on human patients. In the first study, subjects were segregated into controls, controls with APOE4 (a gene linked to increased incidence of Alzheimer's disease), subjects on dihydropyridine based calcium channel blockers and subjects on dihydropyridine based calcium channel blockers and with APOE4. MMSE (Mini Mental Status Examination) test was used to measure cognitive function of each subject. A trajectory of the fitted model versus age can be determined. Figure 17 shows exemplary results of the NLMIXED model of MMSE. This model indicates that subjects on calcium channel blockers show a 4 year lag in cognitive decline relative to subjects not on calcium channel blockers.
[0184] This human association study demonstrated that the use of dihydropyridine calcium channel blockers appears to delay the onset of cognitive decline, suggesting dihydropyridine calcium channel blockers can be used to treat neurodegenerative diseases such as Alzheimer's disease.
[0185] In the second study, we conducted autopsy on a total of 8 subjects from the neuropsychological association study. 4 subjects were on calcium channel blockers, including nifedipine and 4 subjects were not on any calcium channel blocker. Levels of Aβ 1-42 and Aβ processing enzymes such as PS-I, Nicas, BACE, APH-I and PEN-2 in front lobe specimens of subjects were determined using standard methods. Specifically, Aβl-42 levels were determined using Invitrogen ELISAs and protein levels were determined using Western blot analysis and antibodies specific to each protein. As shown in Figure 18, the Aβl-42 level was significantly reduced in subjects with drugs as compared to that in subjects without drugs. Some Aβ processing enzymes including PS-I, Nicas were significantly reduced in those subjects with drugs as compared to those without drugs. Interestingly, the levels of BACE, APH-I and PEN-2 were increased in those subjects with drugs as compared to subjects without drugs.
[0186] In addition, enzyme levels that are involved in Tau phosphorylation were also examined in frontal lobe specimens from the subjects. As shown in Figure 19, the levels of phosphorylated p-Akt, p-GSK-3β and p-ROCK were all increased in subjects with drug as compared to those in subjects without drug. The total protein levels of Akt, GSK-3β and ROCK were comparable in subjects with and without drug. As discussed above, activated p-Akt phosphorylates GSK-3β, which is then inactivated and reduces Tau phosphorylation. These results are consistent with the conclusion that the use of calcium channel blockers can reduce Tau phosphorylation, useful for treatment of Alzheimer's disease.
[0187] This human association study demonstrated that the use of calcium channel blockers appears to reduce Aβl-42 level and certain Aβl-42 processing enzymes, and inactivate enzymes involved in Tau phosphorylation in human patients, indicating calcium channel blockers may be effective in treating Alzheimer's disease.
Example 11. Synthesis of nitroso-nifedipine
[0188] Photochemical synthesis was used in this example to synthesize nitrosonifedipine.
Specifically, nifedipine (20 mg) was dissolved in 10 mL acetonitrile in a pyrex culture tube, capped and photolyzed with a 250W halogen lamp (3M EVW) for 30 minutes. The product was isolated by solvent removal on a rotary evaporator to obtain a blue-green oil (18.1 mg, 94% yield). GC/MS analysis showed greater than 98.5% conversion to nitrosonifedipine. An exemplary result is shown in Figure 20.
Example 12. Treatment of human patients
[0189] A human patient determined to have MCI based on an MMSE score is given nitroso-nifedipine at a dosage of 1000 mg per day. Nitroso-nifedipine is given as tablets for oral administration by patient three times daily.
[0190] Another human patient determined to have early stage Alzheimer's disease (EAD) based on a CDR score is given nitroso-nifedipine at a dosage of 800 mg per day. Nitrosonifedipine is given as tablets for oral administration by patient three times daily. [0191] A human patient determined to have MCI based on the level of PDS/TTR complex in a fluid sample obtained from the patient is given nitroso-nifedipine at a dosage of 1000 mg per day. Nitroso-nifedipine is given as tablets for oral administration by patient four times daily.
EQUIVALENTS
[0192] The foregoing has been a description of certain non- limiting embodiments of the invention. Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents to the specific embodiments of the invention described herein. Those of ordinary skill in the art will appreciate that various changes and modifications to this description may be made without departing from the spirit or scope of the present invention, as defined in the following claims.
[0193] In the claims articles such as "a,", "an" and "the" may mean one or more than one unless indicated to the contrary or otherwise evident from the context. Claims or descriptions that include "or" between one or more members of a group are considered satisfied if one, more than one, or all of the group members are present in, employed in, or otherwise relevant to a given product or process unless indicated to the contrary or otherwise evident from the context. The invention includes embodiments in which exactly one member of the group is present in, employed in, or otherwise relevant to a given product or process. The invention also includes embodiments in which more than one, or all of the group members are present in, employed in, or otherwise relevant to a given product or process. Furthermore, it is to be understood that the invention encompasses all variations, combinations, and permutations in which one or more limitations, elements, clauses, descriptive terms, etc., from one or more of the claims or from relevant portions of the description are introduced into another claim. For example, any claim that is dependent on another claim can be modified to include one or more limitations found in any other claim that is dependent on the same base claim. Furthermore, where the claims recite a composition, it is to be understood that methods of using the composition for any of the purposes disclosed herein are included, and methods of making the composition according to any of the methods of making disclosed herein or other methods known in the art are included, unless otherwise indicated or unless it would be evident to one of ordinary skill in the art that a contradiction or inconsistency would arise. In addition, the invention encompasses compositions made according to any of the methods for preparing compositions disclosed herein.
[0194] Where elements are presented as lists, e.g., in Markush group format, it is to be understood that each subgroup of the elements is also disclosed, and any element(s) can be removed from the group. It is also noted that the term "comprising" is intended to be open and permits the inclusion of additional elements or steps. It should be understood that, in general, where the invention, or aspects of the invention, is/are referred to as comprising particular elements, features, steps, etc., certain embodiments of the invention or aspects of the invention consist, or consist essentially of, such elements, features, steps, etc. For purposes of simplicity those embodiments have not been specifically set forth in haec verba herein. Thus for each embodiment of the invention that comprises one or more elements, features, steps, etc., the invention also provides embodiments that consist or consist essentially of those elements, features, steps, etc.
[0195] Where ranges are given, endpoints are included. Furthermore, it is to be understood that unless otherwise indicated or otherwise evident from the context and/or the understanding of one of ordinary skill in the art, values that are expressed as ranges can assume any specific value within the stated ranges in different embodiments of the invention, to the tenth of the unit of the lower limit of the range, unless the context clearly dictates otherwise. It is also to be understood that unless otherwise indicated or otherwise evident from the context and/or the understanding of one of ordinary skill in the art, values expressed as ranges can assume any subrange within the given range, wherein the endpoints of the subrange are expressed to the same degree of accuracy as the tenth of the unit of the lower limit of the range.
[0196] In addition, it is to be understood that any particular embodiment of the present invention may be explicitly excluded from any one or more of the claims. Any embodiment, element, feature, application, or aspect of the compositions and/or methods of the invention can be excluded from any one or more claims. For purposes of brevity, all of the embodiments in which one or more elements, features, purposes, or aspects is excluded are not set forth explicitly herein.
INCORPORATION OF REFERENCES
[0197] All publications and patent documents cited in this application are incorporated by reference in their entirety to the same extent as if the contents of each individual publication or patent document were incorporated herein.
[0198] What is claimed is:

Claims

1. A pharmaceutical composition suitable for treating, slowing, or preventing Mild Cognitive Impairment (MCI) and/or Alzheimer's disease in a human subject comprising a therapeutically effective amount of an agent selected from the group consisting of nifedipine, oxidized nifedipine, nitroso-nifedipine, thyroxine (T4), triiodothyronine (T3) and combinations thereof, and a pharmaceutically acceptable carrier.
2. The pharmaceutical composition of claim 1, wherein the agent is not a calcium channel blocker.
3. The pharmaceutical composition of claim 1, wherein the agent comprises nifedipine.
4. The pharmaceutical composition of claim 1, wherein the agent comprises oxidized nifedipine.
5. The pharmaceutical composition of claim 1, wherein the agent comprises nitroso-nifedipine.
6. The pharmaceutical composition of claim 1, wherein the agent comprises a mixture of nitroso-nifedipine, oxidized nifedipine, and nifedipine.
7. The pharmaceutical composition of claim 6, wherein the mixture comprises 55% nitroso- nifedipine, 11% oxidized nifedipine, and 34% nifedipine.
8. The pharmaceutical composition of any one of the preceding claims, wherein the agent further comprises thyroxine (T4) and/or triiodothyronine (T3).
9.. The pharmaceutical composition of any one of the preceding claims, wherein the therapeutically effective amount ranges from about 0.01 to about 1000 mg per dose.
10. The pharmaceutical composition of claim 9, wherein the therapeutically effective amount ranges from about 0.01 to about 200 mg per dose.
11. The pharmaceutical composition of claim 9, wherein the therapeutically effective amount ranges from about 0.01 to about 100 mg per dose.
12. The pharmaceutical composition of claim 9, wherein the therapeutically effective amount ranges from about 0.01 to about 50 mg per dose.
13. The pharmaceutical composition of claim 9, wherein the therapeutically effective amount ranges from about 0.01 to about 10 mg per dose.
14. The pharmaceutical composition of claim 9, wherein the therapeutically effective amount ranges from about 0.01 to about 5 mg per dose.
15. The pharmaceutical composition of claim 9, wherein the therapeutically effective amount ranges from about 0.01 to about 2.5 mg per dose.
16. The pharmaceutical composition of claim 9, wherein the therapeutically effective amount ranges from about 0.01 to about 2.0 mg per dose.
17. The pharmaceutical composition of claim 9, wherein the therapeutically effective amount ranges from about 0.01 to about 1.5 mg per dose.
18. The pharmaceutical composition of claim 9, wherein the therapeutically effective amount ranges from about 0.01 to about 1.0 mg per dose.
19. The pharmaceutical composition of claim 9, wherein the therapeutically effective amount ranges from about 0.01 to about 0.5 mg per dose.
20. The pharmaceutical composition of claim 9, wherein the therapeutically effective amount ranges from about 0.01 to about 0.1 mg per dose.
21. The pharmaceutical composition of claim 1, wherein the agent is nitroso-nifedipine and the therapeutically effective amount ranges from about 10 mg to about 2.5 g per dose.
22. The pharmaceutical composition of any one of the preceding claims, wherein the pharmaceutical composition is formulated for administration by a route selected from the group consisting of oral, subcutaneous, intravenous, transdermal, intraperitoneal, intramuscular, intracerebroventricular, intraparenchymal, intrathecal, intracranial, buccal, mucosal, nasal, and rectal administration.
23. The pharmaceutical composition of any one of the preceding claims, wherein the pharmaceutical composition is formulated for oral administration.
24. The pharmaceutical composition of any one of the preceding claims, wherein the pharmaceutical composition is formulated for immediate release.
25. The pharmaceutical composition of any one of claims 1-23, wherein the pharmaceutical composition is formulated for extended release.
26. A method for treating, slowing, or preventing Mild Cognitive Impairment (MCI) and/or Alzheimer's disease in a human subject, the method comprising administering to a subject who is suffering from or susceptible to MCI or Alzheimer's disease a therapeutically effective amount of an agent selected from the group consisting of nifedipine, oxidized nifedipine, nitroso-nifedipine, thyroxine (T4), triiodothyronine (T3) and combinations thereof, such that at least one symptom or feature associated with the MCI or Alzheimer's disease is reduced in abundance, intensity, severity, or frequency, or has delayed onset.
27. The method of claim 26, wherein the agent is not a calcium channel blocker.
28. The method of claim 26, wherein the at least one symptom or feature is cognitive decline.
29. The method of claim 26, wherein the at least one symptom or feature is the production of amyloid beta protein.
30. The method of claim 26, wherein the at least one symptom or feature is beta-secretase activity.
31. The method of claim 26, wherein the at least one symptom or feature is gamma-secretase activity.
32. The method of claim 31 , wherein the gamma-secretase activity is reduced by inhibiting presenilin-1 (PS-I), nicastrin, APH-I and/or PEN-2 activity.
33. The method of claim 31 , wherein the gamma-secretase activity is reduced by inhibiting orphan G-coupled receptor 3 (GPCR-3) activity.
34. The method of claim 26, wherein the at least one symptom or feature is formation of paired helical filaments.
35. The method of claim 34, wherein the at least one symptom or feature is phosphorylated tau protein in the brain.
36. The method of claim 26, wherein the at least one symptom or feature is an immune or inflammatory condition in the central nervous system.
37. The method of claim 36, wherein the immune or inflammatory condition is reduced by decreasing the level of one or more cytokines in the central nervous system.
38. The method of claim 37, wherein the one or more cytokines comprise IL-I.
39. The method of claim 37, wherein the one or more cytokines comprise IL-6.
40. The method of claim 36, wherein the one or more cytokines comprise TNF-α.
41. The method of any one of claims 26-40, wherein the agent comprises nifedipine.
42. The method of any one of claims 26-40, wherein the agent comprises oxidized nifedipine.
43. The method of any one of claims 26-40, wherein the agent comprises nitroso-nifedipine.
44. The method of any one of claims 26-40, wherein the agent comprises a mixture of nitroso-nifedipine, oxidized nifedipine, and nifedipine.
45. The method of claim 44, wherein the mixture comprises 55% nitroso-nifedipine, 11% oxidized nifedipine, and 34% nifedipine.
46. The method of any one of claims 41-45, wherein the agent further comprises thyroxine (T4) and/or triiodothyronine (T3).
47. The method of any one of claims 26-45, wherein the therapeutically effective amount ranges from about 0.01 to about 1000 mg per dose.
48. The method of claim 47, wherein the therapeutically effective amount ranges from about 0.01 to about 200 mg per dose.
49. The method of claim 48, wherein the therapeutically effective amount ranges from about 0.01 to about 100 mg per dose.
50. The method of claim 48, wherein the therapeutically effective amount ranges from about 0.01 to about 50 mg per dose.
51. The method of claim 48, wherein the therapeutically effective amount ranges from about 0.01 to about 10 mg per dose.
52. The method of claim 48, wherein the therapeutically effective amount ranges from about 0.01 to about 5 mg per dose.
53. The method of claim 48, wherein the therapeutically effective amount ranges from about 0.01 to about 2.5 mg per dose.
54. The method of claim 48, wherein the therapeutically effective amount ranges from about 0.01 to about 2.0 mg per dose.
55. The method of claim 48, wherein the therapeutically effective amount ranges from about 0.01 to about 1.5 mg per dose.
56. The method of claim 48, wherein the therapeutically effective amount ranges from about 0.01 to about 1.0 mg per dose.
57. The method of claim 48, wherein the therapeutically effective amount ranges from about 0.01 to about 0.5 mg per dose.
58. The method of claim 48, wherein the therapeutically effective amount ranges from about 0.01 to about 0.1 mg per dose.
59. The method of claim 26, wherein the agent is nitroso-nifedipine and the therapeutically effective amount ranges from about 10 mg to about 2.5 g per dose.
60. The method of any one of claims 26-59, wherein the agent is administered by a route selected from the group consisting of oral, subcutaneous, intravenous, transdermal, intraperitoneal, intramuscular, intracerebroventricular, intraparenchymal, intrathecal, intracranial, buccal, mucosal, nasal, and rectal administration.
61. The method of any one of claims 26-60, wherein the agent is administered by oral administration.
62. The method of any one of claims 26-60, wherein the agent is administered monthly.
63. The method of any one of claims 26-60, wherein the agent is administered bi-weekly.
64. The method of any one of claims 26-60, wherein the agent is administered weekly.
65. The method of any one of claims 26-60, wherein the agent is administered daily.
66. The method of any one of claims 26-60, wherein the agent is administered twice daily
67. The method of any one of claims 26-60, wherein the agent is administered three times a day.
68. The method of any one of claims 26-60, wherein the agent is administered four times daily
69. The method of any one of claims 26-68, wherein the subject has an abnormal level of a biomarker as compared to a control, wherein the biomarker comprises: at least one of a transthyretin protein and/or a prostaglandin-H2 D-isomerase protein, and at least one second, different protein selected from a transthyretin, prostaglandin-H2 D- isomerase, beta-2-microglobulin, cystatin C, superoxide dismutase [Cu-Zn], plasma retinol- binding protein, phosphatidylethanolamine -binding protein, carbonic anhydrase 2, and/or serotransferrin protein.
70. The method of claim 69, wherein the biomarker comprises prostaglandin-D2-synthase and transthyretin (PDS/TTR complex).
71. The method of any one of claims 26-68, wherein the subject has an abnormal level of a biomarker as compared to a control, wherein the biomarker comprises one or more of (i) beta amyloid 40 (Aβ40), (ii) beta amyloid 42 (Aβ42), (iii) the ratio of Aβ40 to Aβ42, and (iv) the ratio of phosphorylated tau to total tau.
72. The method of any one of claims 69-71 , wherein the biomarker is determined in a fluid sample obtained from the subject.
73. The method of claim 72, wherein the fluid sample is selected from the group consisting of CSF, serum, whole blood, blood plasma, urine, ascitic fluid, saliva, tissue effusion, lavage, and combinations thereof.
74. The method of any one of claims 69-73, wherein the control is indicative of a level of the biomarker in a subject selected from the group consisting of a healthy individual, a patient suffering from Alzheimer's disease with a pre-determined stage, the subject before the treatment, and combinations thereof.
75. The method of any one of claims 69-74, wherein the subject has a diminished level of the biomarker as compared to the control.
76. The method of any one of claims 69-74, wherein the subject has an elevated level of the biomarker as compared to the control.
77. The method of any one of claims 69-76, wherein the method further comprises a step of first determining the therapeutically effective amount of the agent based on the abnormal level of the biomarker.
78. The method of any one of claims 26-11 , wherein the subject has a test score indicative of cognitive impairment.
79. The method of claim 78, wherein the test score is an MMSE (Mini Mental Status Examination) score.
80. The method of claim 79, wherein the MMSE score is lower than 27.
81. The method of claim 80, wherein the MMSE score ranges from 21 -26.
82. The method of claim 78, wherein the test score is a clinical dementia rating (CDR) score.
83. The method of claim 82, wherein the CDR score is above 0.
84. The method of claim 83, wherein the CDR score is 0.5 or 1.
85. A solid oral dosage form comprising nitroso-nifedipine and nifedipine, and wherein the mass ratio of nitroso-nifedipine to nifedipine is at least about 1 :1.
86. The solid oral dosage form of claim 85, wherein the mass ratio of nitroso-nifedipine to nifedipine is at least about 2:1.
87. The solid oral dosage form of claim 85, wherein the mass ratio of nitroso-nifedipine to nifedipine is at least about 4:1.
88. The solid oral dosage form of claim 85, wherein the mass ratio of nitroso-nifedipine to nifedipine is at least about 8:1.
89. The solid oral dosage form of claim 85, wherein the mass ratio of nitroso-nifedipine to nifedipine is at least about 16:1.
90. The solid oral dosage form of claim 85, wherein the mass ratio of nitroso-nifedipine to nifedipine is at least about 32:1.
91. The solid oral dosage form of claim 85, wherein the mass ratio of nitroso-nifedipine to nifedipine is at least about 64:1.
92. The solid oral dosage form of claim 85, wherein the mass ratio of nitroso-nifedipine to nifedipine is at least about 100:1.
93. The solid oral dosage form of claim 85, wherein the mass ratio of nitroso-nifedipine to nifedipine is at least about 200:1.
94. The solid oral dosage form of claim 85, wherein the mass ratio of nitroso-nifedipine to nifedipine is at least about 500:1.
95. The solid oral dosage form of claim 85, wherein the mass ratio of nitroso-nifedipine to nifedipine is at least about 1000:1.
96. The solid oral dosage form of any of claims 85-95, further comprising one or more pharmaceutically acceptable excipients.
97. The solid oral dosage form of claim 96, wherein the one or more pharmaceutically acceptable excipients include at least one of a binder, a buffer, a diluent, a dispersant, an emollient, a film-forming agent, a glidant, a light-blocking agent, a preservative, a solvent, a stabilizing agent, a surfactant, a suspending agent, and/or a tonicity agent.
98. The solid oral dosage form of any one of claims 85-97, wherein the solid oral dosage form is formulated for extended release.
99. The solid oral dosage form of any one of claims 85-97, wherein the solid oral dosage form is formulated for immediate release.
PCT/US2010/034721 2009-05-15 2010-05-13 Treatment of mci and alzheimer's disease WO2010132671A1 (en)

Priority Applications (11)

Application Number Priority Date Filing Date Title
CA2761298A CA2761298A1 (en) 2009-05-15 2010-05-13 Treatment of mci and alzheimer's disease
AU2010249015A AU2010249015A1 (en) 2009-05-15 2010-05-13 Treatment of MCI and Alzheimer's disease
JP2012511013A JP2012526844A (en) 2009-05-15 2010-05-13 Treatment of MCI and Alzheimer's disease
EP10775535A EP2429992A4 (en) 2009-05-15 2010-05-13 Treatment of mci and alzheimer's disease
MX2011012015A MX2011012015A (en) 2009-05-15 2010-05-13 Treatment of mci and alzheimer's disease.
PCT/US2010/057287 WO2011142778A1 (en) 2010-05-13 2010-11-18 Treatment of mci and alzheimer's disease
EP10851531.3A EP2568811A4 (en) 2010-05-13 2010-11-18 Treatment of mci and alzheimer's disease
JP2013510067A JP2013526518A (en) 2010-05-13 2010-11-18 Treatment of MCI and Alzheimer's disease
CN2010800680043A CN102984938A (en) 2010-05-13 2010-11-18 Treatment of MCI and Alzheimer's disease
AU2010353287A AU2010353287A1 (en) 2010-05-13 2010-11-18 Treatment of MCI and Alzheimer's disease
CA2799162A CA2799162A1 (en) 2010-05-13 2010-11-18 Treatment of mci and alzheimer's disease

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US21645209P 2009-05-15 2009-05-15
US61/216,452 2009-05-15
US23455109P 2009-08-17 2009-08-17
US61/234,551 2009-08-17

Publications (1)

Publication Number Publication Date
WO2010132671A1 true WO2010132671A1 (en) 2010-11-18

Family

ID=43069025

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2010/034721 WO2010132671A1 (en) 2009-05-15 2010-05-13 Treatment of mci and alzheimer's disease

Country Status (7)

Country Link
US (1) US20100292281A1 (en)
EP (1) EP2429992A4 (en)
JP (1) JP2012526844A (en)
AU (1) AU2010249015A1 (en)
CA (1) CA2761298A1 (en)
MX (1) MX2011012015A (en)
WO (1) WO2010132671A1 (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104507941A (en) * 2012-07-31 2015-04-08 百时美施贵宝公司 Aryl lactam kinase inhibitors
US20180064670A1 (en) * 2015-10-31 2018-03-08 Io Therapeutics, Inc. Treatment of nervous system disorders using combinations of rxr agonists and thyroid hormones
US20190083441A1 (en) * 2017-09-20 2019-03-21 Io Therapeutics, Inc. Treatment of disease with esters of selective rxr agonists
US10596133B2 (en) 2005-09-30 2020-03-24 Io Therapeutics, Inc. Treatment of cancer with specific RXR agonists
US10835507B2 (en) 2016-03-10 2020-11-17 Io Therapeutics, Inc. Treatment of muscular disorders with combinations of RXR agonists and thyroid hormones
US10945976B2 (en) 2011-12-13 2021-03-16 Io Therapeutics, Inc. Autoimmune disorder treatment using RXR agonists
US10946001B2 (en) 2016-03-10 2021-03-16 Io Therapeutics, Inc. Treatment of autoimmune diseases with combinations of RXR agonists and thyroid hormones
US10966950B2 (en) 2019-06-11 2021-04-06 Io Therapeutics, Inc. Use of an RXR agonist in treating HER2+ cancers
US11896558B2 (en) 2021-12-07 2024-02-13 Io Therapeutics, Inc. Use of an RXR agonist and taxanes in treating Her2+ cancers

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2577196C (en) 2004-08-23 2016-01-12 Johannes Herkel Peptide inhibitors for mediating stress responses
US20140088017A1 (en) 2011-05-23 2014-03-27 Yeda Research And Development Co., Ltd. Use of akt phosphorylation as a biomarker for prognosing neurodegenerative diseases and treating same
US20130040303A1 (en) * 2011-08-08 2013-02-14 Eugenia Wang Biomarker for Alzheimer's Disease and/or Mild Cognitive Impairment, and Use Thereof
SG11201408323RA (en) * 2012-06-15 2015-01-29 Found Biomedical Res & Innov Prophylactic and/or therapeutic agent for mild cognitive impairment
US20150045353A1 (en) * 2013-08-09 2015-02-12 Neurogenetic Pharmaceuticals, Inc. Formulations containing gamma secretase modulators, methods for preparation and delivery thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080107601A1 (en) * 2004-10-13 2008-05-08 Ablynx N.V. Nanobodies Tm Against Amyloid-Beta and Polypeptides Comprising the Same for the Treatment of Degenerative Neural Diseases Such as Alzheimer's Disease
US20080194494A1 (en) * 2005-04-26 2008-08-14 Microbia, Inc. 4-Biarylyl-1-Phenylazetidin-2-One Glucuronide Derivatives for Hypercholesterolemia

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2126533A1 (en) * 1971-05-28 1972-12-14 Merck Patent Gmbh, 6100 Darmstadt Process for the production of pharmaceutical preparations
DE4342196A1 (en) * 1993-12-10 1995-06-14 Bayer Ag New 4-phenyl-substituted 1,4-dihydropyridines
IE58110B1 (en) * 1984-10-30 1993-07-14 Elan Corp Plc Controlled release powder and process for its preparation
US5073543A (en) * 1988-07-21 1991-12-17 G. D. Searle & Co. Controlled release formulations of trophic factors in ganglioside-lipsome vehicle
IT1229203B (en) * 1989-03-22 1991-07-25 Bioresearch Spa USE OF 5 METHYLTHETRAHYDROPHOLIC ACID, 5 FORMYLTHETRAHYDROPHOLIC ACID AND THEIR PHARMACEUTICALLY ACCEPTABLE SALTS FOR THE PREPARATION OF PHARMACEUTICAL COMPOSITIONS IN THE FORM OF CONTROLLED RELEASE ACTIVE IN THE THERAPY OF MENTAL AND ORGANIC DISORDERS.
US5120548A (en) * 1989-11-07 1992-06-09 Merck & Co., Inc. Swelling modulated polymeric drug delivery device
US5733566A (en) * 1990-05-15 1998-03-31 Alkermes Controlled Therapeutics Inc. Ii Controlled release of antiparasitic agents in animals
US5580578A (en) * 1992-01-27 1996-12-03 Euro-Celtique, S.A. Controlled release formulations coated with aqueous dispersions of acrylic polymers
IT1270594B (en) * 1994-07-07 1997-05-07 Recordati Chem Pharm CONTROLLED RELEASE PHARMACEUTICAL COMPOSITION OF LIQUID SUSPENSION MOGUISTEIN
EP2311806A3 (en) * 1996-01-29 2011-08-10 The United States of America, Represented by the Secretary, Department of Health and Human Services Dihydropyridine-, pyridine-, benzopyranone- and triazoloquinazoline derivatives, their preparation and their use as adenosine receptor antagonists
WO1999043307A1 (en) * 1998-02-26 1999-09-02 Prange Arthur J Jr Thyroid hormone replacement using sustained release triiodothyronine
EP1069918A4 (en) * 1998-04-08 2002-02-20 Univ Oregon Health Sciences Enhancement of cellular gallium uptake
CA2525970C (en) * 2003-05-15 2011-03-22 Roskamp Research, Llc Use of nilvadipine for reducing amyloid deposition, amyloid neurotoxicity and microgliosis
JP2007512338A (en) * 2003-11-21 2007-05-17 メモリー・ファーマシューティカルズ・コーポレイション Composition and treatment method using L-type calcium channel blocker and cholinesterase inhibitor
PT1874311E (en) * 2005-04-15 2011-11-25 Res & Innovation S P A A method for preventing, delaying or reverting abnormal amyloid deposition
JP2007091664A (en) * 2005-09-29 2007-04-12 Univ Of Tokushima Cell membrane protective agent
WO2007064010A1 (en) * 2005-12-02 2007-06-07 Mochida Pharmaceutical Co., Ltd. Preventive/therapeutic agent for alzheimer's dementia
WO2007112288A2 (en) * 2006-03-23 2007-10-04 Mount Sinai School Of Medicine Cardiovascular composition and use the same for the treatment of alzheimers disease
WO2008051291A2 (en) * 2006-04-11 2008-05-02 Ordway Research Institute Nanoparticle and polymer formulations for thyroid hormone analogs, antagonists, and formulations thereof
JP2009073759A (en) * 2007-09-20 2009-04-09 Univ Of Tokushima Icam-1 expression suppressing agent

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080107601A1 (en) * 2004-10-13 2008-05-08 Ablynx N.V. Nanobodies Tm Against Amyloid-Beta and Polypeptides Comprising the Same for the Treatment of Degenerative Neural Diseases Such as Alzheimer's Disease
US20080194494A1 (en) * 2005-04-26 2008-08-14 Microbia, Inc. 4-Biarylyl-1-Phenylazetidin-2-One Glucuronide Derivatives for Hypercholesterolemia

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
JAVIDNIA ET AL.: "Photostability Determination of Commercially Available Nifedipine Oral Dosage Forms in Iran.", IRANIAN JOURNAL OF PHARMACEUTICAL RESEARCH., vol. 2, no. 2, 2003, pages 111 - 115, XP008165520 *
See also references of EP2429992A4 *
THATHIAH ET AL.: "The Orphan G Protein-Coupled Receptor 3 Modulates Amyloid-Beta Peptide Generation In Neurons.", SCIENCE., vol. 323, 13 February 2009 (2009-02-13), pages 946 - 951, XP002591660 *

Cited By (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10596133B2 (en) 2005-09-30 2020-03-24 Io Therapeutics, Inc. Treatment of cancer with specific RXR agonists
US10973788B2 (en) 2005-09-30 2021-04-13 Io Therapeutics, Inc. Treatment of cancer with specific RXR agonists
US10945976B2 (en) 2011-12-13 2021-03-16 Io Therapeutics, Inc. Autoimmune disorder treatment using RXR agonists
US11793781B2 (en) 2011-12-13 2023-10-24 Io Therapeutics, Inc. Autoimmune disorder treatment using RXR agonists
US11576881B2 (en) 2011-12-13 2023-02-14 Io Therapeutics, Inc. Autoimmune disorder treatment using RXR agonists
US11547684B2 (en) 2011-12-13 2023-01-10 Io Therapeutics, Inc. Autoimmune disorder treatment using RXR agonists
US11246845B2 (en) 2011-12-13 2022-02-15 Io Therapeutics, Inc. Autoimmune disorder treatment using RXR agonists
US11166927B2 (en) 2011-12-13 2021-11-09 Io Therapeutics, Inc. Autoimmune disorder treatment using RXR agonists
CN104507941A (en) * 2012-07-31 2015-04-08 百时美施贵宝公司 Aryl lactam kinase inhibitors
US10702489B2 (en) 2015-10-31 2020-07-07 Io Therapeutics, Inc. Treatment of nervous system disorders using combinations of RXR agonists and thyroid hormones
US11065219B2 (en) 2015-10-31 2021-07-20 Io Therapeutics, Inc. Treatment of nervous system disorders using combinations of RXR agonists and thyroid hormones
US10857117B2 (en) 2015-10-31 2020-12-08 Io Therapeutics, Inc. Treatment of nervous system disorders using combinations of RXR agonists and thyroid hormones
US20180064670A1 (en) * 2015-10-31 2018-03-08 Io Therapeutics, Inc. Treatment of nervous system disorders using combinations of rxr agonists and thyroid hormones
US10278932B2 (en) * 2015-10-31 2019-05-07 Io Therapeutics, Inc. Treatment of nervous system disorders using combinations of RXR agonists and thyroid hormones
US10588881B2 (en) 2015-10-31 2020-03-17 Io Therapeutics, Inc. Treatment of nervous system disorders using combinations of RXR agonists and thyroid hormones
US10806713B2 (en) 2015-10-31 2020-10-20 Io Therapeutics, Inc. Treatment of nervous system disorders using combinations of RXR agonists and thyroid hormones
US10973791B2 (en) 2015-10-31 2021-04-13 Io Therapeutics, Inc. Treatment of nervous system disorders using combinations of RXR agonists and thyroid hormones
US10980760B2 (en) 2015-10-31 2021-04-20 Io Therapeutics, Inc. Treatment of nervous system disorders using combinations of RXR agonists and thyroid hormones
US10980761B2 (en) 2015-10-31 2021-04-20 Io Therapeutics, Inc. Treatment of nervous system disorders using combinations of RXR agonists and thyroid hormones
US10980759B2 (en) 2015-10-31 2021-04-20 Io Therapeutics, Inc. Treatment of nervous system disorders using combinations of RXR agonists and thyroid hormones
US10842764B2 (en) 2015-10-31 2020-11-24 Io Therapeutics, Inc. Treatment of nervous system disorders using combinations of RXR agonists and thyroid hormones
US10695312B2 (en) 2015-10-31 2020-06-30 Io Therapeutics, Inc. Treatment of nervous system disorders using combinations of RXR agonists and thyroid hormones
US10946001B2 (en) 2016-03-10 2021-03-16 Io Therapeutics, Inc. Treatment of autoimmune diseases with combinations of RXR agonists and thyroid hormones
US11690832B2 (en) 2016-03-10 2023-07-04 Io Therapeutics Treatment of autoimmune diseases with combinations of RXR agonists and thyroid hormones
US11690831B2 (en) 2016-03-10 2023-07-04 Io Therapeutics, Inc. Treatment of autoimmune diseases with combinations of RXR agonists and thyroid hormones
US10835507B2 (en) 2016-03-10 2020-11-17 Io Therapeutics, Inc. Treatment of muscular disorders with combinations of RXR agonists and thyroid hormones
US11517549B2 (en) 2017-09-20 2022-12-06 Io Therapeutics, Inc. Treatment of disease with esters of selective RXR agonists
US20190083441A1 (en) * 2017-09-20 2019-03-21 Io Therapeutics, Inc. Treatment of disease with esters of selective rxr agonists
US11224583B2 (en) 2019-06-11 2022-01-18 Io Therapeutics, Inc. Use of an RXR agonist in treating HER2+ cancers
US10966950B2 (en) 2019-06-11 2021-04-06 Io Therapeutics, Inc. Use of an RXR agonist in treating HER2+ cancers
US11896558B2 (en) 2021-12-07 2024-02-13 Io Therapeutics, Inc. Use of an RXR agonist and taxanes in treating Her2+ cancers

Also Published As

Publication number Publication date
EP2429992A1 (en) 2012-03-21
CA2761298A1 (en) 2010-11-18
US20100292281A1 (en) 2010-11-18
EP2429992A4 (en) 2012-11-28
AU2010249015A1 (en) 2011-11-24
MX2011012015A (en) 2012-04-30
JP2012526844A (en) 2012-11-01

Similar Documents

Publication Publication Date Title
US20100292281A1 (en) Treatment of mci and alzheimer&#39;s disease
JP2012526844A5 (en)
Das et al. A close look at BACE1 inhibitors for Alzheimer’s disease treatment
US10874644B2 (en) Therapeutic approaches for treating Alzheimer disease and related disorders through a modulation of synapse function
WO2011142778A1 (en) Treatment of mci and alzheimer&#39;s disease
JP2011518119A (en) Novel uses for 4-phenylbutyric acid (4PBA) and pharmaceutically acceptable salts thereof
US9968574B2 (en) Treatment of MCI and Alzheimer&#39;s disease
AU2017383127B2 (en) Caspase-1 inhibition and uses thereof for prevention and treatment of neurological conditions
CN110891586A (en) S-nitrosoglutathione (GSNO) and GSNO reductase inhibitors for use in therapy
WO2011050095A2 (en) Prevention and treatment of post-operative cognitive dysfunction (pocd)
JP2010531854A (en) Pirenzepine and its derivatives as anti-amyloid agents
KR20110066623A (en) Pharmaceutical composition for preventing or treating diseases associated with beta amyloid accumulation containing epps as an active ingredient
CA2368850C (en) Methods for the prevention and/or the treatment of glutamate cytotoxicity
ES2449594T3 (en) Method to reduce amyloid deposition, amyloid neurotoxicity and microgliosis with enantiomer (-) - nilvadipine
Giubilei Beyond Cholinesterase inhibition: anti-inflammatory role and pharmacological profile of current drug therapy for Alzheimer’s disease
TW202425995A (en) Methods of reducing neurodegeneration associated with neurodegenerative diseases
Ranade et al. TARGET EVOLUTION AND THERAPY ADVANCEMENTS FOR ALZHEIMER’S DISEASE: A REVIEW
WO2013020909A1 (en) Materials and methods for the treatment of tauopathies

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 10775535

Country of ref document: EP

Kind code of ref document: A1

WWE Wipo information: entry into national phase

Ref document number: 2761298

Country of ref document: CA

WWE Wipo information: entry into national phase

Ref document number: 2012511013

Country of ref document: JP

Ref document number: MX/A/2011/012015

Country of ref document: MX

NENP Non-entry into the national phase

Ref country code: DE

ENP Entry into the national phase

Ref document number: 2010249015

Country of ref document: AU

Date of ref document: 20100513

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 2010775535

Country of ref document: EP

REG Reference to national code

Ref country code: BR

Ref legal event code: B01A

Ref document number: PI1012152

Country of ref document: BR

ENP Entry into the national phase

Ref document number: PI1012152

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20111116