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Definitions

• Galactosemia is a metabolic disorder that results from reduced ability or inability to metabolize galactose.
• the disease is typically caused by deficiency of one or more enzymes involved in the Leloir pathway, including galactose- 1 -phosphate uridyl transferase (GALT), galactokinase (GALK), and galactose-6-phosphate epimerase (GALE).
• GALT galactose- 1 -phosphate uridyl transferase
• GALE galactose-6-phosphate epimerase
• Deficiency of one or more of these enzymes results in the disruption of the Leloir pathway and accumulation of galactose and certain galactose metabolites, such as galactose 1 -phosphate (G1P) and galactonate.
• galactose when galactose accumulates, it can become a substrate for aldose reductase (AR), an enzyme in the polyol pathway of glucose metabolism.
• AR aldose reductase
• AR normally catalyzes the reduction of glucose to sorbitol (the first step in the polyol pathway), but can also convert galactose to galactitol when galactose levels are elevated.
• the accumulation of galactose and galactose metabolites can cause damage to the liver, central nervous system (e.g., brain), kidneys, eyes, and other body systems (Quan-Ma et ah, Am J Dis Child., 112(5):477-478, 1966).
• type I galactosemia OMIM #230400
• GALT the second enzyme of the Leloir pathway
• GALK type II galactosemia
• Type III galactosemia OMIM #230350
• All three types are autosomal recessive disorders. Based on the degree of functional impairment of the enzymes (biochemical phenotype), genotype, and potential to develop acute and long-term complications, further subtypes of galactosemias have been identified.
• FIG. 1 is a graph showing weight gain of wild type rat pups (GALT+), GALT null rat pups, and GALT null rat pups treated with aldose reductase inhibitor (ARI) (Compound A), Weight (g) is plotted on the vertical axis and age (days) is plotted on the horizontal axis.
• GALT+ wild type rat pups
• ARI aldose reductase inhibitor
• FIGs. 2A - 2D are charts showing the effect of aldose reductase inhibitors on cataracts in galactosemic rats.
• FIG. 2A shows the results of a qualitative assessment of cataract at day 9 presence/severity score (scale of 0-3) in control (wild-type rats treated with Compound A), and GALT-null rats treated with placebo or Compound A.
• Score 0 indicates no cataracts present;
• score 1 indicates cataracts are mild in size and opacity;
• score 2 indicates cataracts are moderate in size and opacity; and
• score 3 indicates cataracts are severe in size and opacity.
• Cataracts were assessed at day 22 of life.
• FIG. 2C shows the results of a qualitative assessment of cataracts in wild type or GALT null rats treated with Compound B or placebo at day 10 of life.
• FIG. 2D shows a qualitative assessment of cataracts in wild type or GALT null rats treated with Compound B or placebo at day 22 of life. The qualitative analysis in FIGs. 2C and FIG. 2D was performed using the same scoring method as in FIG. 2A. [0009] FIG.
• FIG. 3A-3C are bar charts showing the levels of the metabolites galactitol, galactose, and galactose 1 phosphate in liver, brain or plasma of control (wild-type rats) and GALT-null rats treated with placebo or Compound B.
• FIG. 3A shows galactitol levels
• FIG. 3B shows galactose levels
• FIG. 3C shows galactose-1 -phosphate (GallP) levels.
• This disclosure relates to methods for treating galactosemia and treating or preventing complications of galactosemia by administering an therapeutically effective amount of an AR inhibitor to a subject in need thereof. Without wishing to be bound by any particular theory, and as described herein, it is believed that inhibition of AR can reduce or prevent accumulation of galactitol and resulting pathology associated with galactosemia.
• the method for the treatment or prevention of galactosemia comprises administering to a subject in need thereof an therapeutically effective amount of zopolrestat. In one example, the method for the treatment or prevention of galactosemia (or galactosemia complications) comprises administering to a subject in need thereof an therapeutically effective amount of epalrestat. In one example, the method for the treatment or prevention of galactosemia (or galactosemia complications) comprises administering to a subject in need thereof an therapeutically effective amount of a compound of any one of Formulas I-VI.
• the AR inhibitor administered is not ponalrestat, epalrestat, sorbinil or sorbinol, imirestat, AND-138, CT-112, zopolrestat, zenarestat, BAL-AR18, AD-5467, M-79175, tolrestat, alconil, statil, berberine or SPR-210.
• the subject to be treated in accordance with the methods disclosed herein can have increased alditol levels in blood, urine or intraocular fluid, such as elevated galactitol, myoinositol or sorbitol levels in blood, urine or intraocular fluid.
• the subject to be treated in accordance with the methods disclosed herein can have complications or manifestations of galactosemia that include liver cirrhosis, retinal disorder, macular edema, eye cataract, ovarian dysfunction, muscle or nerve dysfunction, retinopathy, neuropathy, cognitive dysfunction, motor ataxia, seizure, pseudomotor cerebrii, speech dysfunction impaired neural conduction or mental retardation.
• the disclosure relates to a method of treating or preventing complications associated with galactosemia in a subject in need thereof comprising, administering an therapeutically effective amount of a pharmaceutical composition comprising AR inhibitor and a pharmaceutically acceptable carrier.
• the disclosure relates to a method of reducing the amount or level of galactitol in a subject with galactosemia, comprising administering a therapeutically effective amount of an aldose reductase inhibitor to the subject.
• the disclosure relates to a method for treating cataracts, comprising administering a therapeutically effective amount of an aldose reductase inhibitor to a subject in need thereof.
• the subject in need thereof has galactosemia.
• the disclosure relates to a method for treating or preventing cognitive or neurological deficiency associated with galactosemia, comprising administering a therapeutically effective amount of an aldose reductase inhibitor to a subject with galactosemia.
• the cognitive or neurological deficiency associated with galactosemia is speech dysfunction.
• the cognitive or neurological deficiency associated with galactosemia is motor ataxia.
• the cognitive or neurological deficiency associated with galactosemia is cognitive dysfunction.
• the cognitive or neurological deficiency associated with galactosemia is pseudomotor cerebrii.
• the cognitive or neurological deficiency associated with galactosemia is seizure.
• the disclosure relates to a method of treating or preventing galactosemia in a subject in need thereof comprising, administering an therapeutically effective amount of (a) a first pharmaceutical composition comprising a compound of Formulas I - VI and a pharmaceutically acceptable carrier; and
• a second pharmaceutical composition comprising alponalrestat, epalrestat, sorbinil or sorbinol, imirestat, AND-138, CT-112, zopolrestat, zenarestat, BAL-AR18, AD-5467, M- 79175, tolrestat, alconil, statil, berberine or SPR-210 and a pharmaceutically acceptable carrier.
• an AR inhibitor for inhibiting the production of alditol (e.g., galactitol) for therapy of galactosemia.
• an AR inhibitor for the manufacture of a medicament for treating galactosemia or a clinical manifestation of galactosemia selected from cataracts and primary ovarian insufficiency (POI).
• the disclosure also relates to the use of an AR inhibitor (e.g., zopolrestat, epalrestat, compound of any one of Formulas I - VI) for the treatment of galactosemia and/or the treatment and prevention of complications associated with galactosemia.
• an AR inhibitor e.g., zopolrestat, epalrestat, compound of any one of Formulas I - VI
• the disclosure also relates to an AR inhibitor (e.g., zopolrestat, epalrestat, compound of any one of Formulas I - VI) for the manufacture of a medicament for treatment of galactosemia and/or the treatment and prevention of complications associated with galactosemia.
• an AR inhibitor e.g., zopolrestat, epalrestat, compound of any one of Formulas I - VI
• the disclosure also relates to a pharmaceutical formulation for treatment of galactosemia and/or the treatment and prevention of complications associated with galactosemia, that contains an AR inhibitor (e.g., zopolrestat, epalrestat, compound of any one of Formulas I - VI) as an active ingredient.
• an AR inhibitor e.g., zopolrestat, epalrestat, compound of any one of Formulas I - VI
• This disclosure relates to the use of AR inhibitors for the treatment of galactosemia.
• the methods described herein are based in part on the inventor's insights into the role of AR activity in the pathophysiology of galactosemia.
• AR primarily catalyzes the reduction of glucose to sorbitol (the first step in polyol pathway of glucose metabolism).
• This accumulation of galactitol causes or contributes to the pathophysiological events in galactosemic tissues, such as, hypertonicity, sugar imbalance, oxidative stress, and the like. Accordingly, this disclosure relates to methods for treating or preventing galactosemia or complications of galactosemia by administering an therapeutically effective amount of an AR inhibitor to a subject in need thereof. Without wishing to be bound by any particular theory, it is believed that inhibition of AR can reduce or prevent accumulation of galactitol and resulting pathology and complications associated with galactosemia.
• These complications may be mediated, in part, via increased synthesis of galactitol and/or increased accumulation of galactitol (e.g., due to deficiency or insufficiency in the enzymes of the Leloir pathway, elevated galactose levels, aberrant AR activity, reduced excretion of galactitol from the tissues (e.g., due to kidney disorders)).
• Inhibition of aldose reductase can reduce the synthesis and buildup of galactitol in tissues and resulting pathology and complications associated with galactosemia.
• the present disclosure further relates to the use of galactitol as a biomarker of aldose reductase inhibition, and also, as a biomarker for monitoring the initiation, progression, and manifestation of galactosemia.
• the word “about” means a range of plus or minus 10% of that value, e.g., "about 50” means 45 to 55, "about 25,000” means 22,500 to 27,500, etc., unless the context of the disclosure indicates otherwise, or is inconsistent with such an interpretation.
• “about 49, about 50, about 55, "about 50” means a range extending to less than half the interval(s) between the preceding and subsequent values, e.g., more than 49.5 to less than 52.5.
• the phrases “less than about” a value or “greater than about” a value should be understood in view of the definition of the term "about” provided herein.
• this disclosure includes descriptions of various components, groups of components, ranges and other elements of the broader disclosure. It is intended that such elements can be variously combined to provide additional embodiments of the disclosure. It is also intended that any disclosed features (e.g., substituent, analog, compound, structure, component) including individual members of any disclosed group, including any sub-ranges or combinations of sub-ranges within the group, may be excluded from the disclosure or any embodiments of the disclosure for any reason.
• the disclosure relates to a method for the treatment of galactosemia (or galactosemia complications), comprising administering to a subject in need thereof an therapeutically effective amount of a compound that inhibits aldose reductase activity.
• the method is particularly useful for the treatment and/or prevention of complications associated with galactosemia.
• the compound can be any suitable compound that inhibits AR activity, such as a small molecule compound (e.g., having a size of 5 kDa or less), a biologic agent (e.g., an inhibitory RNA directed against aldose reductase) or a combination thereof.
• the AR inhibitor is a small molecule compound. Suitable small molecule AR inhibitors are known in the art and are disclosed herein.
• Small molecule AR inhibitors include ponalrestat, sorbinil, sorbinol, imirestat, AND-138, CT-112, zenarestat, BAL-AR18, AD-5467, M-79175, tolrestat, alconil, statil, berberine, SPR-210 zopolrestat, epalrestat, the compounds disclosed in US 8,916,563, US 9,650,383, and the compounds disclosed herein.
• Preferred AR inhibitors for use in the invention include zopolrestat, epalrestat, the compounds disclosed in US Pat. No. 8,916,563, US Pat. No. 9,650,383, and the compounds disclosed herein.
• the AR inhibitors can be administered in any molecular suitable form including pharmaceutically acceptable salts, solvates, prodrugs, and compounds that contain stable isotopic forms of one or more atoms, e.g., deuterium in place of hydrogen.
• the method for the treatment of galactosemia comprises administering to a subject in need thereof an therapeutically effective amount of zopolrestat.
• the disclosure provide a method for the treatment of galactosemia and prevention of galactosemia complications in a patient with galactosemia and comprises administered to a subject in need thereof a therapeutically effective amount of zopolrestat.
• the method for the treatment of galactosemia comprises administering to a subject in need thereof an therapeutically effective amount of epalrestat.
• the disclosure provide a method for the treatment of galactosemia and prevention of galactosemia complications in a patient with galactosemia and comprises administered to a subject in need thereof a therapeutically effective amount of epalrestat.
• the method for the treatment of galactosemia comprises administering to a subject in need thereof an therapeutically effective amount of an aldose reductase, wherein the aldose reductase inhibitor is not ponalrestat, epalrestat, sorbinil or sorbinol, imirestat, AND-138, CT-1 12, zopolrestat, zenarestat, BAL-AR18, AD-5467, M-79175, tolrestat, alconil, statil, berberine or SPR-210.
• the aldose reductase inhibitor is not ponalrestat, epalrestat, sorbinil or sorbinol, imirestat, AND-138, CT-1 12, zopolrestat, zenarestat, BAL-AR18, AD-5467, M-79175, tolrestat, alconil, statil, berberine or SPR-210.
• the method for the treatment of galactosemia comprises administering to a subject in need thereof an therapeutically effective amount of a compound of any one of Formulas I-VI.
• the disclosure provide a method for the treatment of galactosemia and prevention of galactosemia complications in a patient with galactosemia and comprises administering to a subject in need thereof a therapeutically effective amount of a compound of any one of Formulas I-VI.
• the compound that is administered is Compound A or the compound that is administered is Compound B.
• the term “treating” refers to curative or palliative (e.g., control or mitigate a disease or disease symptoms) therapy. This can include reversing, reducing, arresting or delaying the symptoms, clinical signs, and underlying pathology of galactosemia in a manner to improve or stabilize a subject's condition.
• the term "preventing" within the context of the present method refers to a prophylactic treatment of an individual with galactosemia, e.g., to prevent complications (e.g., symptom and clinical signs) associated with galactosemia.
• a family history or predisposition to diabetes can indicate that the subject is at risk for galactosemia and related complications.
• the method can be used for treatment of galactosemia, treatment of complications (e.g., symptoms and clinical signs) of galactosemia, and/or treatment and prevention of complications (e.g., symptoms and clinical signs) of galactosemia.
• a therapeutically effective amount is an amount of a compound that is sufficient to achieve the desired therapeutic effect under the conditions of administration, such as an amount that reduces or ameliorates the severity and/or duration of galactosemia or one or more clinical manifestations thereof (e.g., cataracts or primary ovarian insufficiency (POI)), that prevents the advancement of conditions or symptoms related to galactosemia, or enhances or otherwise improves therapeutic effect(s) of another therapy for the treatment or management of galactosemia (e.g., hormonal therapy in the case of POI or surgery in the case of cataracts).
• POI primary ovarian insufficiency
• a therapeutically effective amount can be an amount that reduces and preferably normalizes the amount or level of galactose or a galactose metabolite, in particular galactitol, in the subject being treated.
• the actual amount administered can be determined by an ordinarily skilled clinician based upon, for example, the subjects age, weight, sex, general heath and tolerance to drugs, severity of disease, dosage form selected, route of administration and other factors.
• the amount of an AR inhibitor that is administered is from about 0.5 to about 60 mg/kg body weight per day, such as from about 1.0 to 10 mg/kg.
• the therapeutically effective amount is an amount sufficient to reduce intracellular aldose reductase activity at least by about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, about 90%, about 95%, about 99%, or more, e.g., about 100% (e.g., compared to pre- treatment level).
• the therapeutically effective amount can be an amount that reduces intracellular galactitol levels at least by about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, about 90%, about 95%, about 99%, or more, e.g., about 100% (e.g., compared to pre-treatment level).
• the therapeutically effective amount can be an amount that reduces plasma galactitol concentration to less than 200 ⁇ , particularly less than 100 ⁇ , especially less than 50 ⁇ , and preferably less than 10 ⁇ in a human subject with galactosemia.
• Plasma galactitol levels are elevated in untreated classical galactosemia patients (120-500 ⁇ /1) compared to controls (0.08-0.86 ⁇ /1). (Jakobs et ah, Eur J Pediatr., 154(7 Suppl 2): S50-2, 1995).
• the therapeutically effective amount can be sufficient to restore a physiological trait that is diminished in galactosemia, e.g., diminished eyesight in the case of cataractic subjects or reduced estrogen levels in a subject with POI.
• a therapeutically effective amount of an aldose reductase inhibitor can be an amount that is sufficient to normalize galactitol levels in tissues (e.g., liver galactitol levels, brain galactitol levels) or the blood
• a "subject" can be any animal, particularly a mammal, and including, but by no means limited to, humans, domestic animals, such as feline or canine subjects, farm animals, such as but not limited to bovine, equine, caprine, ovine, avian and porcine subjects, wild animals (whether in the wild or in a zoological garden), research or laboratory animals, such as mice, rats, rabbits, goats, sheep, pigs, dogs, cats, etc., avian species, such as chickens, turkeys, songbirds, and the like.
• the "subject” is a human who is predisposed to (due to genetic aberration) or has been diagnosed with galactosemia.
• a human subject to be treated using the methods disclosed herein is diagnosed with galactosemia as a new born through enzymatic or genetic screening, and has deficiency in GALT activity, GALK activity or GALE activity.
• This disclosure also relates to the prophylaxis or treatment of at least one clinical feature or complication of galactosemia in a subject.
• Representative clinical features or complications which can be present in children, adolescents or adults, include, e.g., liver dysfunction, susceptibility to infections, failure to thrive, cataracts, retinopathy, neuropsychological and ovarian problems.
• the disclosure relates to treatment of at least one trait of galactosemic subjects selected from jaundice (incidence: 74% of subjects), vomiting (47% of subjects), hepatomegaly (43% of subjects), failure to thrive (29% of subjects), poor feeding (23% of subjects), lethargy (16% of subjects), diarrhea (12% of subjects), sepsis (10 % of subjects), more specifically, E.
• coli sepsis (76% of sepsis), coagulopathy, ascites, seizures, hepatomegaly, hypotonia, edema, full fontanelle, encephalopathy, and excessive bruising or bleeding, primary ovarian insufficiency and premature ovarian failure (POF).
• POF premature ovarian failure
• the clinical feature is lenticular cataracts, retinopathy, or ovarian dysfunction (e.g., primary ovarian insufficiency (POI) or premature ovarian failure (POF)).
• POI primary ovarian insufficiency
• POF premature ovarian failure
• IQ impaired executive function
• tremor ataxia
• dysarthria dysarthria
• apraxia of speech depression and anxiety.
• additional preferred clinical features of galactosemia that can be treated or prevented using the methods described herein are neurological and cognitive deficiencies, such as central nervous system deficiencies including speech dysfunctions (e.g., delayed or impaired speech), motor ataxia, seizure, pseudomotor cerebrii and cognitive dysfunction (e.g., low IQ (IQ below about 85)).
• the disclosure relates to a method for the treatment of a clinical feature or complication of galactosemia and comprises administering to a subject in need thereof an therapeutically effective amount of zopolrestat.
• the disclosure relates to a method for the treatment of a clinical feature or complication of galactosemia and comprises administering to a subject in need thereof an therapeutically effective amount of epalrestat.
• the disclosure relates to a method for the treatment of a clinical feature or complication of galactosemia and comprises administering to a subject in need thereof an therapeutically effective amount of a compound of any one of Formulas I-VI.
• the clinical feature or complication of galactosemia to be treated or prevented is retinopathy or cataracts.
• Presenile cataracts are a common complication in patients with galactosemia, and in particular embodiments, the method is a method for treating cataracts.
• the cataracts can be subcapsular cataracts occurring at the back of the lens, nuclear cataracts which form in the central zone (nucleus) of the lens, and cortical (spoke-like) cataracts affecting the lens cortex.
• the methods are also useful in the treatment of cataracts that have been or are being treated with surgery, cataracts that occur after surgical removal of an existing opacified lens, i.e., secondary cataracts, cataracts that occur after retinal detachment and surgery to repair the retinal detachment, cataracts associated with trauma to the eye or head, cataracts associated with tumors, cataracts associated with exposure to radiation, and cataracts associated with sugar toxicity.
• the present methods are also useful in the prophylactic treatment of cataracts resulting from systemic disorders, for example, but not limited to, galactosemia.
• the clinical feature or complication of galactosemia to be treated or prevented is a long-term neurological and cognitive complication of galactosemia.
• Patients with galactosemia can experience long-term neurological and cognitive complications, even when the disease is diagnosed early and is managed with a galactose-restricted diet.
• Such complications are variable, and include below average IQ, impaired executive function, tremor, ataxia, dysarthria, apraxia of speech, depression and anxiety.
• the clinical feature or complication of galactosemia to be treated or prevented is primary ovarian insufficiency (POI) or premature ovarian failure (POF), or a symptom related thereto.
• POI primary ovarian insufficiency
• POF premature ovarian failure
• the method comprises administering to a subject in need thereof, a compound of the disclosure or a composition containing the compound.
• POI is characterized by dysfunctional ovaries (e.g., inability to produce estrogen and other hormones that are important to reproductive health).
• Galactosemia is one of the few known causes of POI and almost all women with galactosemia have POI or develop it at some point in their lives.
• Symptoms or traits associated with POI include, e.g., delayed onset of period, sudden stoppage or disruption in period, malformation of breasts, hot flashes, affect disorders, e.g., mood swings or irritability, vaginal dryness, and/or inability to sleep.
• the disclosure relates to a method for reducing the amount or level of galactitol in a subject, comprising administering to a subject in need thereof an therapeutically effective amount of a compound that inhibits aldose reductase activity.
• the method can be used to reduce galactitol in tissues, such as liver, brain, eye, retina, and/or in the circulation (e.g., blood or plasma) and/or in urine.
• the galactitol levels are normalized.
• Galactose levels can be elevated in patients with galactosemia, and preferably, the method of reducing galactitol does not cause further elevation of galactose levels.
• Normal amounts or levels of galactitol are the amounts or levels present in health subjects who are not on a restricted diet. Such normal amounts or levels are well known and shown in Table 1.
• the clinical feature or complication of galactosemia to be treated or prevented is retinopathy or cataracts.
• Presenile cataracts are a common complication in patients with galactosemia, and in particular embodiments, the method is a method for treating cataracts.
• the cataracts can be subcapsular cataracts occurring at the back of the lens, nuclear cataracts that form in the central zone (nucleus) of the lens, and cortical (spokelike) cataracts affecting the lens cortex.
• the methods are also useful in the treatment of cataracts that have been or are being treated with surgery, cataracts that occur after surgical removal of an existing opacified lens, i.e., secondary cataracts, cataracts that occur after retinal detachment and surgery to repair the retinal detachment, cataracts associated with trauma to the eye or head, cataracts associated with tumors, cataracts associated with exposure to radiation, and cataracts associated with sugar toxicity.
• the present methods are also useful in the prophylactic treatment of cataracts resulting from systemic disorders, for example, but not limited to, galactosemia.
• the disclosure relates to a method for the treatment or prevention of cataracts and comprises administering to a subject in need thereof a therapeutically effective amount of zopolrestat.
• the disclosure relates to a method for the treatment or prevention of cataracts and comprises administering to a subject in need thereof a therapeutically effective amount of epalrestat.
• the disclosure relates to a method for the treatment or prevention of cataracts and comprises administering to a subject in need thereof a therapeutically effective amount of a compound of any one of Formulas I- VI.
• the compound that is administered is Compound A or the compound that is administered is Compound B.
• the patient in need of therapy for the treatment or prevention of cataracts has galactosemia.
• the clinical feature or complication of galactosemia to be treated or prevented is a long-term neurological and cognitive complication of galactosemia.
• Patients with galactosemia can experience long-term neurological and cognitive complications, even when the disease is diagnosed early and is managed with a galactose-restricted diet.
• Such complications are variable, and include below average IQ, impaired executive function, tremor, ataxia, dysarthria, apraxia of speech, depression and anxiety.
• the disclosure relates to a method for the treatment or prevention of neurological and cognitive deficiencies associated with galactosemia and comprises administering to a subject with galactosemia a therapeutically effective amount of zopolrestat.
• the neurological or cognitive deficiency associated with galactosemia is speech dysfunction, such as delayed speech or impaired speech.
• the neurological or cognitive deficiency associated with galactosemia is motor ataxia.
• the neurological or cognitive deficiency associated with galactosemia is cognitive dysfunction, such as low IQ.
• the neurological or cognitive deficiency associated with galactosemia is pseudomotor cerebrii.
• the neurological or cognitive deficiency associated with galactosemia is seizure.
• the disclosure relates to a method for the treatment or prevention of neurological and cognitive deficiencies associated with galactosemia and comprises administering to a subject with galactosemia a therapeutically effective amount of epalrestat.
• the neurological or cognitive deficiency associated with galactosemia is speech dysfunction, such as delayed speech or impaired speech.
• the neurological or cognitive deficiency associated with galactosemia is motor ataxia.
• the neurological or cognitive deficiency associated with galactosemia is cognitive dysfunction, such as low IQ.
• the neurological or cognitive deficiency associated with galactosemia is pseudomotor cerebrii.
• the neurological or cognitive deficiency associated with galactosemia is seizure.
• the disclosure relates to a method for the treatment or prevention of neurological and cognitive deficiencies associated with galactosemia and comprises administering to a subject with galactosemia a therapeutically effective amount of a compound of any one of Formulas I-VI.
• the compound that is administered is Compound A or the compound that is administered is Compound B.
• the neurological or cognitive deficiency associated with galactosemia is speech dysfunction, such as delayed speech or impaired speech.
• the neurological or cognitive deficiency associated with galactosemia is motor ataxia.
• the neurological or cognitive deficiency associated with galactosemia is cognitive dysfunction, such as low IQ.
• the neurological or cognitive deficiency associated with galactosemia is pseudomotor cerebrii.
• the neurological or cognitive deficiency associated with galactosemia is seizure.
• the clinical feature or complication of galactosemia to be treated or prevented is primary ovarian insufficiency (POI) or premature ovarian failure (POF), or a symptom related thereto.
• POI primary ovarian insufficiency
• POF premature ovarian failure
• the method comprises administering to a subject in need thereof, a compound of the disclosure or a composition containing the compound.
• POI is characterized by dysfunctional ovaries (e.g., inability to produce estrogen and other hormones, which are important to reproductive health).
• Galactosemia is one of the few known causes of POI and almost all women with galactosemia have POI or develop it at some point in their lives.
• Symptoms or traits associated with POI include, e.g., delayed onset of period, sudden stoppage or disruption in period, malformation of breasts, hot flashes, affect disorders, e.g., mood swings or irritability, vaginal dryness, and/or inability to sleep.
• the disclosure relates to a method for the treatment or prevention of POI or POF and comprises administering to a subject with galactosemia a therapeutically effective amount of zopolrestat.
• the disclosure relates to a method for the treatment or prevention of POI or POF and comprises administering to a subject with galactosemia a therapeutically effective amount of epalrestat.
• the disclosure relates to a method for the treatment or prevention of POI or POF and comprises administering to a subject with galactosemia a therapeutically effective amount of a compound of any one of Formulas I-VI.
• the compound that is administered is Compound A or the compound that is administered is Compound B.
• the disclosure relates to a method for reducing the amount or level of galactitol in a subject, comprising administering to a subject in need thereof an therapeutically effective amount of a compound that inhibits aldose reductase activity.
• the method can be used to reduce galactitol in tissues, such as liver, brain, eye, retina, and/or in the circulation (e.g., blood or plasma) and/or in urine.
• the galactitol levels are normalized.
• Galactose levels can be elevated in patients with galactosemia, and preferably, the method of reducing galactitol does not cause further elevation of galactose levels.
• Normal amounts or levels of galactitol are the amounts or levels present in health subjects who are not on a restricted diet. Such normal amounts or levels are well known and shown in Table 1.
• the disclosure relates to a method for reducing, and preferably normalizing, the amount or level of galactitol in a subject with galactosemia and comprises administering to a subject in need thereof a therapeutically effective amount of zopolrestat.
• the disclosure relates to a method for reducing, and preferably normalizing, the amount or level of galactitol in a subject with galactosemia and comprises administering to a subject in need thereof a therapeutically effective amount of epalrestat.
• the disclosure relates to a method for reducing, and preferably normalizing, the amount or level of galactitol in a subject with galactosemia and comprises administering to a subject in need thereof a therapeutically effective amount of a compound of any one of Formulas I-VI.
• the compound that is administered is Compound A or the compound that is administered is Compound B.
• the aforementioned methods are carried out by administering a formulation comprising a single dosage or single administration (e.g., as a single injection or deposition) of one or more AR inhibitors.
• the methods are carried out by administering formulations that are adapted for administration once daily, twice daily, three times daily or four times daily to a subject in need thereof for a period of from about 2 to about 28 days, or from about 7 to about 10 days, or from about 7 to about 15 days, or longer.
• the methods are carried out by administering formulations that are adapted for chronic administration.
• the methods are carried out by administering formulations that are adapted for administration over the course of several weeks, months, years or decades.
• the methods are carried out by administering formulations that are adapted for administration over the course of several weeks. In still other embodiments, the methods are carried out by administering formulations that are adapted for administration over the course of several months. In still other embodiments, the methods are carried out by administering formulations that are adapted for administration over the course of several years. In still other embodiments, the methods are carried out by administering formulations that are adapted for administration over the course of several decades.
• Suitable small molecule AR inhibitors are known in the art and are disclosed herein.
• Small molecule AR inhibitors include ponalrestat, sorbinil, sorbinol, imirestat, AND- 138, CT-112, zenarestat, BAL-AR18, AD-5467, M-79175, tolrestat, alconil, statil, berberine, SPR- 210, zopolrestat, epalrestat, the compounds disclosed in US 8,916,563, US 9,650,383, WO2012/009553 and the compounds disclosed herein.
• Preferred AR inhibitors for use in the invention zopolrestat, epalrestat, the compounds disclosed in US Pat. No. 8,916,563, US Pat. No.
• the AR inhibitor is a compound of Formula (I) or pharmaceutically acceptable salts, prodrugs and solvates thereof,
• R 1 is H, (Ci-C 6 )-alkyl, (Ci-C6)-hydroxyalkyl, or (Ci-C 6 )-aminoalkyl;
• X 1 is N or CR 3 ;
• X 2 is N or CR 4 ;
• X 3 is N or CR 5 ;
• X 4 is N or CR 6 ; with the proviso that two or three of X 1 , X 2 , X 3 , or X 4
• a 1 is NR. 11 , O, S or CH 2 ;
• a 2 is N or CH
• a 3 is NR 11 , O, or S;
• R 3 through R 10 are independently hydrogen, halogen, cyano, acyl, haloalkyl, haloalkoxy, haloalkylthio, trifluoroacetyl, (Ci-C4)-alkyl, (Ci-C4)-alkoxy, (Ci-C4)-alkylthio,
• R 10 taken together are (Ci-C4)-alkylenedioxy
• R n is hydrogen, Ci-C 4 alkyl, or C(0)0-(Ci-C 4 )-alkyl.
• RMs hydrogen or (Ci-C6)-alkyl. In certain embodiments, RMs hydrogen. In certain embodiments, RMs (Ci-C6)-alkyl. In certain embodiments, RMs tert-butyl.
• R 3 through R 10 are independently hydrogen, halogen or haloalkyl. In certain embodiments, R 3 through R 10 are independently hydrogen, halogen or trihaloalkyl.
• R 3 through R 6 are hydrogen.
• R 7 through R 10 are independently hydrogen, halogen or haloalkyl. In certain embodiments, R 7 through R 10 are independently hydrogen, halogen or trihaloalkyl.
• R 7 and R 10 are hydrogen.
• R 8 is hydrogen, halogen or haloalkyl. In certain embodiments, R 8 is hydrogen. In certain embodiments, R 8 is halogen. In certain embodiments, R 8 is haloalkyl.
• R 9 is hydrogen, halogen or haloalkyl. In certain embodiments, R 9 is hydrogen. In certain embodiments, R 9 is halogen. In certain embodiments, R 9 is haloalkyl.
• a 1 is NR 11 , S or CH2. In certain embodiments, AHs NR n or O. In certain embodiments, A 1 is NR n or S. In certain embodiments, A 1 is NR 11 . In certain embodiments, A 1 is O. In certain embodiments, A 1 is S.
• a 2 is N or CH. In certain embodiments, A 1 is N. In certain embodiments, A 1 is CH.
• a 3 is O or S. In certain embodiments, A 3 is O. In certain embodiments, A 3 is S.
• X 1 and X 4 are nitrogen.
• X 1 and X 2 are nitrogen.
• X 1 and X 3 are nitrogen.
• X 2 and X 3 are nitrogen.
• X 2 and X 4 are nitrogen.
• X 3 and X 4 are nitrogen.
• Z is
• Z is
• R 1 is hydrogen or (Ci-C6)-alkyl
• X 1 and X 4 are N;
• X 2 is CR 4 ;
• X 3 is CR 5 ;
• AMsNR 11 O, or S
• a 2 is N;
• a 3 isO, orS
• R 4 and R 5 are hydrogen
• R 7 through R 10 are independently hydrogen, halogen, cyano, acyl, haloalkyl, haloalkoxy, haloalkylthio.
• R 11 is hydrogen, Ci-C 4 alkyl, or C(0)0— (Ci-C 4 )-alkyl.
• R 1 is hydrogen or tert-butyl
• X 2 isCR 4 ;
• X 3 isCR 5 ;
• a 2 is N;
• a 3 is O or S
• R 4 and R 5 are hydrogen
• R 7 through R 10 are independently hydrogen, halogen, or haloalkyl; and 0126] R n is hydrogen, (Ci-C 4 )-alkyl, or C(0)0-tert-butyl.
• R 1 is hydrogen or tert-butyl
• X 1 and X 4 are N;
• X 2 is CH
• X 3 is CH
• a 1 is NR
• a 2 is N;
• a 3 is O or S
• R 7 , R 8 and R 10 are independently hydrogen, halogen, or haloalkyl
• R 9 is halogen, or haloalkyl
• R 11 is hydrogen or methyl.
• R 1 is hydrogen or tert-butyl
• X 1 and X 4 are N;
• X 2 is CH
• X 3 is CH
• a 1 is NR 11 , O or S
• a 2 is N;
• a 3 is O or S
• R 7 , R 8 and R 10 are independently hydrogen, halogen, or haloalkyl
• R 9 is chlorine, or trifluoromethyl
• R 11 is hydrogen or methyl.
• the AR inhibitor is a compound of Formula (II) or pharmaceutically acceptable salt or solvate thereof:
• exemplary compounds of Formula II include the following and salts thereof:
• the AR inhibitors can be a compound of Formula (III) or pharmaceutically acceptable salts, pro-drugs and solvates thereof,
• R 1 is CO2R 2 or C0 2 X + ;
• R 2 is H, (Ci-C 6 )-alkyl, (Ci-C 6 )-hydroxyalkyl, or (Ci-C6)-aminoalkyl;
• X 1 is H or halogen
• X 2 is H or halogen
• a 1 is NR 7 , O, S or CH 2 ;
• a 2 is N or CH
• a 3 is NR 7 , O, or S;
• R 3 through R 6 are independently hydrogen, halogen, cyano, acyl, haloalkyl, haloalkoxy, haloalkylthio, trifluoroacetyl, (Ci-C4)-alkyl, (Ci-C4)-alkoxy, (Ci-C4)-alkylthio, (Ci-C4)-alkylsulfinyl, or (Ci-C4)-alkylsulfonyl;
• R 7 is hydrogen, Ci-C 4 alkyl, or C(0)0-(Ci-C 4 )-alkyl
• X + is a counter ion.
• Z is or Z is indicates that when Z is
• R 1 is CO2R 2 or CC " X + . In certain embodiments, R 1 is CO2R 2 . In certain embodiments, R 1 is C02 " X + .
• R 2 is hydrogen or (Ci-C6)-alkyl. In certain embodiments, R 2 is hydrogen or (Ci-C4)-alkyl. In certain embodiments, R 2 is hydrogen or (Ci-C3)-alkyl. In certain embodiments, R 2 is hydrogen, methyl, or ethyl. In certain embodiments, R 2 is hydrogen or methyl. In certain embodiments, R 2 is methyl or ethyl. In certain embodiments, R 2 is methyl. In certain embodiments, R 2 is hydrogen. In certain embodiments, R 2 is (Ci- C6)-alkyl. In certain embodiments, R 2 is (Ci-C6)- «-alkyl.
• R 2 is (Ci- C2)-alkyl. In certain embodiments, R 2 is (Ci-C3)-alkyl. In certain embodiments, R 2 is (Ci- C4)-alkyl. In certain embodiments, R 2 is tert-butyl.
• R 3 through R 6 are independently hydrogen, halogen, cyano, acyl, haloalkyl, haloalkoxy, haloalkylthio, trifluoroacetyl, (Ci-C4)-alkyl, (Ci-C4)-alkoxy, (Ci-C 4 )-alkylthio, (Ci-C4)-alkylsulfinyl, or (Ci-C4)-alkylsulfonyl.
• R 3 through R 6 are independently hydrogen, halogen or haloalkyl. In certain embodiments, R 3 through R 6 are independently hydrogen, halogen or trihaloalkyl.
• R 3 and R 6 are hydrogen. In certain embodiments, R 3 , R 5 , and R 6 are hydrogen. [0179] In certain embodiments, R 4 is hydrogen, halogen or haloalkyl. In certain embodiments, R 4 is hydrogen. In certain embodiments, R 4 is halogen. In certain embodiments, R 4 is haloalkyl. I n certain embodiments, R 4 is CF3.
• R 3 through R 6 are hydrogen. In certain embodiments, R 3 , R 5 , R 6 are hydrogen and R 4 is halogen or haloalkyl. In certain embodiments, R 3 , R 5 , R 6 are hydrogen and R 4 is haloalkyl. In certain embodiments, R 3 , R 5 , R 6 are hydrogen and R 4 is CF3. In certain embodiments, R 3 , R 5 , R 6 are hydrogen and R 4 is halogen. In certain embodiments, R 3 , R 5 , R 6 are hydrogen and R 4 is F. In certain embodiments, R 3 , R 5 , R 6 are hydrogen and R 4 is CI.
• a 1 is NR 7 , O, S or CH2. In certain embodiments, A 1 is NR 7 , O, or S. In certain embodiments, A 1 is NR 7 , S or CH2. In certain embodiments, A 1 is NR 7 or O. In certain embodiments, A 1 is NR 7 or S. In certain embodiments, A 1 is NR 7 . In certain embodiments, A 1 is O. In certain embodiments, A 1 is S.
• a 2 is N or CH. In certain embodiments, A 2 is N. In certain embodiments, A 2 is CH.
• a 3 is NR 7 , O, or S. In certain embodiments, A 3 is O. In certain embodiments, A 3 is S. In certain embodiments, A 3 is NR 7 .
• X 1 and X 2 are hydrogen.
• X 1 and X 2 are halogen. In certain embodiments, X 1 and X 2 are CI. [0187] In certain embodiments, X 1 and X 2 are independently hydrogen or halogen. In certain embodiments, X 1 is hydrogen and X 2 is CI. In certain embodiments, X 1 is CI and X 2 is hydrogen.
• Z is
• Z is
• R 7 is hydrogen, C1-C4 alkyl, or C(0)0-(Ci-C4)-alkyl. In certain embodiments, R 7 is hydrogen. In certain embodiments, R 7 is C1-C4 alkyl. In certain embodiments, R 7 is C1-C3 alkyl. In certain embodiments, R 7 is C1-C2 alkyl. In certain embodiments, R 7 is C1-C4 «-alkyl. In certain embodiments, R 7 is C1-C3 «-alkyl. In certain embodiments, R 7 is C(0)0-(Ci-C4)-alkyl. In certain embodiments, R 7 is C(0)0-(Ci-C3)- alkyl.
• R 7 is C(0)0-(Ci-C2)-alkyl. In certain embodiments, R 7 is C(0)0-(Ci-C 4 )- «-alkyl. In certain embodiments, R 7 is C(0)0-(Ci-C 3 )- «-alkyl.
• R 1 is CO2R 2 ;
• R 2 is H or (Ci-C 6 )-alkyl
• X 1 is H
• X 2 is H
• a 1 is NR 7 , O, or S; [0198] A 2 is N;
• a 3 is O or S
• R 3 through R 6 are independently hydrogen, halogen, cyano, acyl, haloalkyl, haloalkoxy, haloalkylthio, trifluoroacetyl, (Ci-C4)-alkyl, (Ci-C4)-alkoxy, (Ci-C4)-alkylthio,
• R 7 is hydrogen, Ci-C 4 alkyl, or C(0)0-(Ci-C 4 )-alkyl.
• R 1 is CO2R 2 ;
• R 2 is H or tert-but l
• X 1 is H
• X 2 is H
• a 1 is NR 7 , O, or S
• a 2 is N;
• a 3 is O or S
• R 6 through R 6 are independently hydrogen, halogen, haloalkyl
• R 7 is hydrogen, C1-C4 alkyl, or C(0)0-(Ci-C 4 )-alkyl.
• R 1 is CO2R 2 ;
• R 2 is H or tert-butyl
• X 1 is H
• X 2 is H
• a 1 is NR 7 , 0, or S
• a 2 is N:
• a 3 is 0 or S:
• R 3 , R 5 , and R 6 are hydrogen
• R 4 is hydrogen, halogen, or haloalkyl
• R 7 is hydrogen, Ci-C 4 alkyl, or C(0)0-(Ci-C 4 )-alky
• R 1 is CO2R 2 ;
• R 2 is H or (Ci-C6)-alkyl
• X 1 is halogen
• X 2 is halogen
• a 1 is NR 7 , O, or S;
• a 2 is N;
• a 3 is O or S
• R 3 through R 6 are independently hydrogen, halogen, cyano, acyl, haloalkyl, haloalkoxy, haloalkylthio. trifluoroacetyl, (Ci-C4)-alkyl. (Ci-C4)-alkoxy, (Ci-C4)-alkylthio,
• R 7 is hydrogen, C1-C4 alkyl, or C(0)0-(Ci-C 4 )-alkyl.
• R 1 is CO2R 2 ;
• R 2 is H or tert-but l;
• X 1 is halogen
• X 2 is halogen
• a 1 is NR 7 , O, or S
• a 2 is N;
• a 3 is O or S
• R 3 through R 6 are independently hydrogen, halogen, haloalkyl
• R 7 is hydrogen, C1-C4 alkyl, or C(0)0-(Ci-C 4 )-alkyl.
• R 1 is CO2R 2 ;
• R 2 is H or tert-butyl
• X 1 is CI
• X 2 is CI
• a 2 is N;
• a 3 is O or S
• R 3 through R 6 are independently hydrogen, halogen, haloalkyl
• R 7 is hydrogen, C1-C4 alkyl, or C(0)0-(Ci-C4)-alkyl.
• R 1 is CO2R 2 ;
• R 2 is H or tert-but l
• X 1 is CI
• X 2 is CI
• a 1 is NR 7 , O, or S
• a 2 is N;
• a 3 is O or S
• R 3 , R 5 , and R 6 are hydrogen
• R 4 is hydrogen, halogen, or haloalkyl
• R 7 is hydrogen, C1-C4 alkyl, or C(0)0-(Ci-C 4 )-alkyl.
• the compound of Formula (III) is selected from the
• the compound of Formula (I) is N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoe-N-(2-aminoe-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethy
• the compound of formula (I) is N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoe-N-(2-aminoe-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoe
• the AR inhibitors can be a compound of Formula (IV) or pharmaceutically acceptable salts, and solvates thereof,
• X 2 is H or halogen
• Z 1 and Z 2 are independently selected from the group consisting of hydroxy, alkoxy, aryloxy, or Z 1 and Z 2 taken together with the boron atom to which they are bonded form
• X is a substituted or unsubstituted C2-C5 alkylene
• a 1 is NR 7 , O, S or CH 2 ;
• a 2 is N or CH
• a 3 is NR 7 , O, or S;
• R 3 through R 6 are independently hydrogen, halogen, cyano, acyl, haloalkyl, haloalkoxy, haloalkylthio, trifluoroacetyl, (Ci-C4)-alkyl, (Ci-C4)-alkoxy, (Ci-C4)-alkylthio, (Ci-C4)-alkylsulfinyl, or (Ci-C4)-alkylsulfonyl; and
• R 7 is hydrogen, C1-C4 alkyl, or C(0)0-(Ci-C 4 )-alkyl.
• Suitable substituents on the C2-C5 alkylene include one or more alkyl, alkoxy, aryl, aryloxy, halo, haloalkyl, haloalkoxy, haloalkylthio.
• a preferred substituted C2-C5 alkylene is substituted ethylene.
• a more preferred substituted C2-C5 alkylene is -C(CH3)2C(CH3)2- [0290] It will be recognized by those of skill in the art that the designation of indicates that when Z is , the compounds of Formula (IV) are understood to encompass of Formula (IV) are understood to
• Z 1 and Z 2 are independently selected from the group consisting of hydroxy, alkoxy, aryloxy, or Z 1 and Z 2 taken together with the boron atom to which they are bonded form
• X is a substituted or unsubstituted C2-C5 alkylene.
• R 3 through R 6 of Formula (IV) are independently hydrogen, halogen, cyano, acyl, haloalkyl, haloalkoxy, haloalkylthio, trifluoroacetyl, (Ci-C4)-alkyl, (Ci-C4)-alkoxy, (Ci-C 4 )-alkylthio, (Ci-C4)-alkylsulfmyl, or (Ci-C4)-alkylsulfonyl.
• R 3 through R 6 of Formula (IV) are independently hydrogen, halogen or haloalkyl. In certain embodiments, R 3 through R 6 are independently hydrogen, halogen or trihaloalkyl.
• R 3 and R 6 of Formula (IV) are hydrogen. In certain embodiments, R 3 , R 5 , and R 6 are hydrogen.
• R 4 of Formula (IV) is hydrogen, halogen or haloalkyl. In certain embodiments, R 4 is hydrogen. In certain embodiments, R 4 is halogen. In certain embodiments, R 4 is haloalkyl. In certain embodiments, R 4 is CF3.
• R 3 through R 6 of Formula (IV) are hydrogen.
• R 3 , R 5 , R 6 are hydrogen and R 4 is halogen or haloalkyl.
• R 3 , R 5 , R 6 are hydrogen and R 4 is haloalkyl.
• R 3 , R 5 , R 6 are hydrogen and R 4 is CF3.
• R 3 , R 5 , R 6 are hydrogen and R 4 is halogen.
• R 3 , R 5 , R 6 are hydrogen and R 4 is F.
• R 3 , R 5 , R 6 are hydrogen and R 4 is CI.
• a 1 of Formula (IV) is NR 7 , O, S or CH2. In certain embodiments, A 1 is NR 7 , O, or S. In certain embodiments, A 1 is NR 7 , S or CH2. In certain embodiments, A 1 is NR 7 or O. In certain embodiments, A 1 is NR 7 or S. In certain embodiments, A 1 is NR 7 . In certain embodiments, A 1 is O. In certain embodiments, A 1 is S.
• a 2 of Formula (IV) is N or CH. In certain embodiments, A 2 is N. In certain embodiments, A 2 is CH.
• a 3 of Formula (IV) is NR 7 , O, or S. In certain embodiments, A 3 is O. In certain embodiments, A 3 of Formula (IV) is S. In certain embodiments, A 3 is NR 7 .
• X 1 and X 2 of Formula (IV) are hydrogen.
• X 1 and X 2 of Formula (IV) are halogen. In certain embodiments, X 1 and X 2 are CI.
• X 1 and X 2 of Formula (IV) are independently hydrogen or halogen.
• X 1 is hydrogen and X 2 is CI.
• X 1 is CI and X 2 is hydrogen.
• R 7 of Formula (IV) is hydrogen, C1-C4 alkyl, or C(0)0- (Ci-C4)-alkyl. In certain embodiments, R 7 is hydrogen. In certain embodiments, R 7 is C1-C4 alkyl. In certain embodiments, R 7 is C1-C3 alkyl. In certain embodiments, R 7 is C1-C2 alkyl. In certain embodiments, R 7 is C1-C4 «-alkyl. In certain embodiments, R 7 is C1-C3 «-alkyl. In certain embodiments, R 7 is C(0)0-(Ci-C4)-alkyl.
• R 7 is C(0)0- (Ci-C3)-alkyl. In certain embodiments, R 7 is C(0)0-(Ci-C2)-alkyl. In certain embodiments, R 7 is C(0)0-(Ci-C4)- «-alkyl. In certain embodiments, R 7 is C(0)0-(Ci-C3)- «-alkyl.
• Z 1 and Z 2 are independently selected from the group consisting of hydroxy, alkoxy, aryloxy, or Z 1 and Z 2 taken together with the boron atom to which they are bonded form
• X is a substituted or unsubstituted C2-C5 alkylene.
• Z 1 and Z 2 are independently selected from the group consisting of hydroxy, alkoxy, aryloxy, or Z 1 and Z 2 taken together with the boron atom to which they are bonded form
• X is a substituted or unsubstituted C2-C5 alkylene.
• Z 1 and Z 2 are independently selected from the group consisting of hydroxy, alkoxy, aryloxy, or Z 1 and Z 2 taken together with the boron atom to which they are bonded form
• X is a substituted or unsubstituted C2-C5 alkylene.
• Z 1 and Z 2 are independently selected from the group consisting of hydroxy, alkoxy, aryloxy, or Z 1 and Z 2 taken together with the boron atom to which they are bonded form
• X is a substituted or unsubstituted C2-C5 alkylene.
• the aldose reductase inhibitor is a compound of Formula (V)
• X 3 is N or CR 8 ;
• X 4 is N or CR 9 ;
• X 5 is N or CR 10 ;
• X 6 is N or CR 11 ; with the proviso that two or three of X 3 , X 4 , X 5 , or X 6 are N;
• Z 1 and Z 2 are independently selected from the group consisting of hydroxy, alkoxy, aryloxy, or Z 1 and Z 2 taken together with the boron atom to which they are bonded form
• X is a substituted or unsubstituted C2-C5 alkylene
• a 4 is NR 16 , O, S or CH 2 ;
• a 5 is N or CH
• a 6 is NR 16 , O, or S;
• R 8 through R 15 are independently hydrogen, halogen, cyano, acyl, haloalkyl, haloalkoxy, haloalkylthio, trifluoroacetyl, (Ci-C4)-alkyl, (Ci-C4)-alkoxy, (Ci-C4)-alkylthio, (Ci-C4)-alkylsulfinyl, or (Ci-C4)-alkylsulfonyl; or two of R 8 through R 11 or two of R 12 through R 15 taken together are (Ci-C4)-alkylenedioxy; and
• R 16 is hydrogen, Ci-C 4 alkyl, or C(0)0-(Ci-C 4 )-alkyl.
• Suitable substituents on the C2-C5 alkylene include one or more alkyl, alkoxy, aryl, aryloxy, halo, haloalkyl, haloalkoxy, haloalkylthio.
• a preferred substituted C2-C5 alkylene is substituted ethylene.
• a more preferred substituted C2-C5 alkylene is -C(CH3)2C(CH3)2- [0366] It will be recognized by those of skill in the art that the designation of
• the compounds of Formula (V) are understood to encompass (Va); and when Z is , the compounds
• R 8 through R 15 are independently hydrogen, halogen or haloalkyl, for example, R 8 through R 15 are independently hydrogen, halogen or trihaloalkyl (e.g., -CF3).
• R 8 through R 11 are hydrogen.
• R 12 through R 15 are independently hydrogen, halogen or haloalkyl, for example, R 12 through R 15 are independently hydrogen, halogen or trihaloalkyl (e.g., -CF3).
• R 12 and R 15 of Formula (V) are hydrogen.
• R 13 of Formula (V) is hydrogen, halogen or haloalkyl. In certain embodiments, R 13 is hydrogen. In certain embodiments, R 13 is halogen. In certain embodiments, R 13 is haloalkyl.
• R 14 of Formula (V) is hydrogen, halogen or haloalkyl. In certain embodiments, R 14 is hydrogen. In certain embodiments, R 14 is halogen. In certain embodiments, R 14 is haloalkyl.
• a 4 of Formula (V) is NR 16 , S or CH2. In certain embodiments, A 4 is NR 16 or O. In certain embodiments, A 4 is NR 16 or S. In certain embodiments, A 4 is NR 16 . In certain embodiments, A 4 is O. In certain embodiments, A 4 is S.
• a 5 of Formula (V) is N or CH. In certain embodiments, A 4 is N. In certain embodiments, A 4 is CH.
• a 6 of Formula (V) is O or S. In certain embodiments, A 6 is O. In certain embodiments, A 6 is S.
• X 3 and X 6 of Formula (V) are nitrogen.
• X 3 and X 4 of Formula (V) are nitrogen.
• X 3 and X 5 of Formula (V) are nitrogen.
• X 4 and X 5 of Formula (V) are nitrogen.
• X 4 and X 6 of Formula (V) are nitrogen.
• X 5 and X 6 of Formula (V) are nitrogen.
• Z 3 of Formula (V) is
• Z 3 of Formula (V) is
• R 14 is hydrogen, halogen or trihaloalkyl (e.g., -CF3);
• Z 1 and Z 2 are independently selected from the group consisting of hydroxy, alkoxy. aryloxy, or Z 1 and Z 2 taken together with the boron atom to which they are bonded form
• X is a substituted or unsubstituted C2-C5 alkylene.
• the aldose reductase inhibitor is a compound of Formula (VI)
• Z 1 and Z 2 are independently selected from the group consisting of hydroxy, alkoxy, aryloxy, or Z 1 and Z 2 taken together with the boron atom to which they are bonded form
• X is a substituted or unsubstituted C2-C5 alkylene.
• the AH inhibitor of Formula (VI) is N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N-(2-aminoethyl)-2-aminoethyl-N
• alkyl refers to a monovalent aliphatic hydrocarbon radical having a straight chain, branched chain, monocyclic moiety, or polycyclic moiety or combinations thereof, wherein the radical is optionally substituted at one or more carbons of the straight chain, branched chain, monocyclic moiety, or polycyclic moiety or combinations thereof with one or more substituents at each carbon, where the one or more substituents are independently C1-C10 alkyl.
• alkyl groups include methyl, ethyl, propyl, isopropyl, butyl, iso-but l, sec-butyl, tert-butyl, pentyl, hexyl, heptyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, norbornyl, and the like.
• halogen or "halo-”, as used herein, means chlorine (CI), fluorine (F), iodine (I) or bromine (Br).
• acyl is used in a broad sense to designate radicals of the type RCO-, in which R represents an organic radical which may be an alkyl, aralkyl, aryl, alicyclic or heterocyclic radical, substituted or unsubstituted, saturated or unsaturated; or, differently defined, the term “acyl” is used to designate broadly the monovalent radicals left when the OH group of the carboxylic radical is removed from the molecule of a carboxylic acid.
• alkoxy is employed to designate a group of the formula: -O-R wherein R is an alkyl group, which optionally contains substituents, such as halogen.
• R is an alkyl group, which optionally contains substituents, such as halogen.
• alkoxy is employed to designate an alkoxy with an alkyl group of 1 to 6 carbon atoms.
• alkoxy is employed to designate an alkoxy with an alkyl group of 1 to 3 carbon atoms, such as methoxy or ethoxy.
• cycloalkyl group is used herein to identify cycloalkyl groups having 3-6 carbon atoms preferably cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl.
• solvate means a compound, or a pharmaceutically acceptable salt thereof, wherein molecules of a suitable solvent are incorporated in the crystal lattice.
• a suitable solvent is physiologically tolerable at the dosage administered. Examples of suitable solvents are ethanol, water and the like. When water is the solvent, the molecule is referred to as a "hydrate.”
• a "prodrug” refers to an agent, which is converted into the parent drug in vivo. Prodrugs are often useful because, in some situations, they are easier to administer than the parent drug. They are bioavailable, for instance, by oral administration whereas the parent drug is either less bioavailable or not bioavailable. The prodrug also has improved solubility in pharmaceutical compositions over the parent drug.
• the compound carries protective groups which are split off by hydrolysis in body fluids, e.g., in the bloodstream, thus releasing active compound or is oxidized or reduced in body fluids to release the compound.
• the term “prodrug” may apply to such functionalities as, for example; the acid functionalities of the compounds of formula I.
• Prodrugs may be comprised of structures wherein an acid group is masked, for example, as an ester or amide. Further examples of prodrugs are discussed herein. See also Alexander et al. (J. Med. Chem. 1988, 31, 318), which is incorporated by reference. Examples of prodrugs include, but are not limited to, derivatives and metabolites of a compound that include biohydrolyzable moieties such as biohydrolyzable amides, biohydrolyzable esters, biohydrolyzable carbamates, biohydrolyzable carbonates, and biohydrolyzable phosphate analogues.
• biohydrolyzable moieties such as biohydrolyzable amides, biohydrolyzable esters, biohydrolyzable carbamates, biohydrolyzable carbonates, and biohydrolyzable phosphate analogues.
• prodrugs are also described in, for example, The Practice of Medicinal Chemistry (Camille Wermuth, ed., 1999, Academic Press; hereby incorporated by reference in its entirety).
• prodrugs of compounds with carboxyl functional groups are the lower alkyl esters of the carboxylic acid.
• the carboxylate esters are conveniently formed by esterifying any of the carboxylic acid moieties present on the molecule.
• Prodrugs can typically be prepared using well-known methods, such as those described by Burger 's Medicinal Chemistry and Drug Discovery 6 th ed. (Donald J. Abraham ed., 2001, Wiley) and Design and Application of Prodrugs (H.
• Biohydrolyzable moieties of a compound of Formula I do not interfere with the biological activity of the compound but can confer upon that compound advantageous properties in vivo, such as uptake, duration of action, or onset of action; or (b) may be biologically inactive but are converted in vivo to the biologically active compound.
• biohydrolyzable esters include, but are not limited to, lower alkyl esters, alkoxyacyloxy esters, alkyl acylamino alkyl esters, and choline esters.
• biohydrolyzable amides include, but are not limited to, lower alkyl amides, a-amino acid amides, alkoxyacyl amides, and alkylaminoalkylcarbonyl amides.
• biohydrolyzable carbamates include, but are not limited to, lower alkylamines, substituted ethylenediamines, amino acids, hydroxyalkylamines, heterocyclic and heteroaromatic amines, and poly ether amines.
• salt includes salts derived from any suitable of organic and inorganic counter ions well known in the art and include, by way of example, hydrochloric acid salt or a hydrobromic acid salt or an alkaline or an acidic salt of the aforementioned amino acids.
• salts derived from inorganic or organic acids including, for example hydrochloric, hydrobromic, sulfuric, nitric, perchloric, phosphoric, formic, acetic, lactic, maleic, fumaric, succinic, tartaric, glycolic, salicylic, citric, methanesulfonic, benzenesulfonic, benzoic, malonic, trifluoroacetic, trichloroacetic, naphthalene-2 sulfonic and other acids; and salts derived from inorganic or organic bases including, for example sodium, potassium, calcium, ammonium or tetrafluoroborate.
• Exemplary pharmaceutically acceptable salts are found, for example, in Berge, et al. (J. Pharm. Set 1977, 66(1), 1 ; and U.S. Pat. Nos. 6,570,013 and 4,939,140; each hereby incorporated by reference in its entirety).
• Pharmaceutically acceptable salts are also intended to encompass hemi-salts, wherein the ratio of compound: acid is respectively 2: 1.
• Exemplary hemi-salts are those salts derived from acids comprising two carboxylic acid groups, such as malic acid, fumaric acid, maleic acid, succinic acid, tartaric acid, glutaric acid, oxalic acid, adipic acid and citric acid.
• exemplary hemi-salts are those salts derived from diprotic mineral acids such as sulfuric acid.
• Exemplary preferred hemi-salts include, but are not limited to, hemimaleate, hemifumarate, and hemisuccinate.
• the term "acid” contemplates all pharmaceutically acceptable inorganic or organic acids.
• Inorganic acids include mineral acids such as hydrohalic acids, such as hydrobromic and hydrochloric acids, sulfuric acids, phosphoric acids and nitric acids.
• Organic acids include all pharmaceutically acceptable aliphatic, alicyclic and aromatic carboxylic acids, dicarboxylic acids, tricarboxylic acids, and fatty acids.
• Preferred acids are straight chain or branched, saturated or unsaturated C1-C20 aliphatic carboxylic acids, which are optionally substituted by halogen or by hydroxyl groups, or C6-C12 aromatic carboxylic acids.
• acids are carbonic acid, formic acid, fumaric acid, acetic acid, propionic acid, isopropionic acid, valeric acid, alpha-hydroxy acids, such as glycolic acid and lactic acid, chloroacetic acid, benzoic acid, methane sulfonic acid, and salicylic acid.
• dicarboxylic acids include oxalic acid, malic acid, succinic acid, tartaric acid and maleic acid.
• a tricarboxylic acid is citric acid.
• Fatty acids include all pharmaceutically acceptable saturated or unsaturated aliphatic or aromatic carboxylic acids having 4 to 24 carbon atoms. Examples include butyric acid, isobutyric acid, sec-butyric acid, lauric acid, palmitic acid, stearic acid, oleic acid, linoleic acid, linolenic acid, and phenylsteric acid.
• Other acids include gluconic acid, glycoheptonic acid and lactobionic acid.
• compositions are physiologically acceptable and typically include the active compound and a carrier.
• carrier refers to a diluent, adjuvant, excipient, or vehicle with which a compound is administered.
• Non-limiting examples of such pharmaceutical carriers include liquids, such as water and oils, including those of petroleum, animal, vegetable or synthetic origin, such as peanut oil, soybean oil, mineral oil, sesame oil and the like.
• the pharmaceutical carriers may also be saline, gum acacia, gelatin, starch paste, talc, keratin, colloidal silica, urea, and the like.
• auxiliary, stabilizing, thickening, lubricating and coloring agents may be used.
• suitable pharmaceutical carriers are described in Remington's Pharmaceutical Sciences (Alfonso Gennaro ed., Krieger Publishing Company (1997); Remington's: The Science and Practice of Pharmacy, 21 st Ed. (Lippincot, Williams & Wilkins (2005); Modem Pharmaceutics, vol. 121 (Gilbert Banker and Christopher Rhodes, CRC Press (2002); each of which hereby incorporated by reference in its entirety).
• the carrier can be suitable for ocular applications, e.g., application into the eye for the treatment of eye diseases, e.g., cataract.
• the carrier may comprise a suppository for vaginal administration, e.g., for the treatment of premature ovarian insufficiency (POI).
• POI premature ovarian insufficiency
• the composition can be in a desired form, such as a table, capsule, solution, emulsion, suspension, gel, sol, or colloid that is physiologically and/or pharmaceutically acceptable.
• the carrier can include a buffer, for example with alkaline buffers, e.g., ammonium buffer, acidic buffers, e.g., ethanoates, citrates, lactates, acetates, etc., or zwitterionic buffers, such as, glycine, alanine, valine, leucine, isoleucine and phenylalanine, Kreb's-Ringer buffer, TRIS, MES, ADA, ACES, PIPES, MOPSO, cholamine chloride, MOPS, BES, TES, HEPES, DIPSO, MOBS, TAPSO, acetamidoglycine, TEA, POPSO, HEPPSO, EPS, HEPPS, Tricine, TRIZMA, Glycinamide
• a carrier can be a solvent or dispersion medium comprising but not limited to, water, ethanol, polyol ⁇ e.g., glycerol, propylene glycol, liquid polyethylene glycol, etc.), lipids ⁇ e.g., triglycerides, vegetable oils, liposomes) and combinations thereof.
• the proper fluidity can be maintained, for example, by the use of a coating, such as lecithin; by the maintenance of the required particle size by dispersion in carriers such as, for example liquid polyol or lipids; by the use of surfactants such as, for example hydroxypropylcellulose; or combinations thereof such methods.
• tonicity adjusting agents can be included, such as, for example, sugars, sodium chloride or combinations thereof.
• the composition is isotonic.
• compositions may also include additional ingredients, such as acceptable surfactants, co-solvents, emollients, agents to adjust the pH and osmolarity and/or antioxidants to retard oxidation of one or more component.
• additional ingredients such as acceptable surfactants, co-solvents, emollients, agents to adjust the pH and osmolarity and/or antioxidants to retard oxidation of one or more component.
• compositions can be prepared for administration by any suitable route such as ocular (including periocular and intravitreal administration), oral, parenteral, intranasal, anal, vaginal, topical, subcutaneous, intravenous, intra-arterial, intrathecal and intraperitoneal administration.
• oral administration of aldose reductase inhibitors effectively lowered and normalized galactitol levels in blood and tissues include brain.
• intrathecal administration is an option and may be selected by a clinician (e.g., when the aldose reductase inhibitor is not central nervous system penetrant), it is generally preferred that the aldose reductase inhibitor is not administered intrathecally.
• the composition may be formulated as, for example, drops, solutions, suspensions, emulsions, ointments, sustained release formulation, troche, elixir, syrup, wafer, powder or combinations thereof. See, Gaudana et al, AAPS J, 12(3): 348-360, 2010. Oral compositions may be incorporated directly with the food of the diet.
• Preferred carriers for oral administration comprise inert diluents, edible carriers or combinations thereof.
• pharmaceutically acceptable carriers may include, for example, water or saline solution, polymers such as polyethylene glycol, carbohydrates and derivatives thereof, oils, fatty acids, or alcohols.
• Surfactants such as, for example, detergents, are also suitable for use in the formulations.
• surfactants include polyvinylpyrrolidone, polyvinyl alcohols, copolymers of vinyl acetate and of vinylpyrrolidone, polyethylene glycols, benzyl alcohol, mannitol, glycerol, sorbitol or polyoxyethylenated esters of sorbitan; lecithin or sodium carboxymethylcellulose; or acrylic derivatives, such as methacrylates and others, anionic surfactants, such as alkaline stearates, in particular sodium, potassium or ammonium stearate; calcium stearate or triethanolamine stearate; alkyl sulfates, in particular sodium lauryl sulfate and sodium cetyl sulfate; sodium dodecylbenzenesulphonate or sodium dioctyl sulphosuccinate; or fatty acids, in particular those derived from coconut oil, cationic surfactants, such as water-soluble quaternary ammonium salts of formula
• an oral composition may comprise one or more binders, excipients, disintegration agents, lubricants, flavoring agents, and combinations thereof.
• a composition may comprise one or more of the following: a binder, such as, for example, gum tragacanth, acacia, cornstarch, gelatin or combinations thereof; an excipient, such as, for example, dicalcium phosphate, mannitol, lactose, starch, magnesium stearate, sodium saccharine, cellulose, magnesium carbonate or combinations thereof; a disintegrating agent, such as, for example, corn starch, potato starch, alginic acid or combinations thereof; a lubricant, such as, for example, magnesium stearate; a sweetening agent, such as, for example, sucrose, lactose, saccharin or combinations thereof; a flavoring agent, such as, for example peppermint, oil of wintergreen, cherry flavoring, orange flavoring, etc., or combinations thereof
• Additional formulations which are suitable for other modes of administration include suppositories.
• sterile injectable solutions may be prepared using an appropriate solvent.
• dispersions are prepared by incorporating the various sterilized amino acid components into a sterile vehicle, which contains the basic dispersion medium and/or the other ingredients. Suitable formulation methods for any desired mode of administration are well known in the art (see, generally, Remington's Pharmaceutical Sciences, 18 th Ed. Mack Printing Company, 1990).
• Typical pharmaceutically acceptable compositions can contain a an AR inhibitor and/or a pharmaceutically acceptable salt thereof at a concentration ranging from about 0.01 to about 2 wt%, such as 0.01 to about 1 wt% or about 0.05 to about 0.5 wt%.
• the composition can be formulated as a solution, suspension, ointment, or a capsule, and the like.
• the pharmaceutical composition can be prepared as an aqueous solution and can contain additional components, such as preservatives, buffers, tonicity agents, antioxidants, stabilizers, viscosity-modifying ingredients and the like. Other equivalent modes of administration can be found in U.S. Patent No. 4,939,140.
• the AR inhibitor and pharmaceutically acceptable carriers can be sterile. Suitable pharmaceutical carriers may also include excipients such as starch, glucose, lactose, sucrose, gelatin, malt, rice, flour, chalk, silica gel, sodium stearate, glycerol monostearate, talc, sodium chloride, dried skim milk, glycerol, propylene, glycol, polyethylene glycol 300, water, ethanol, polysorbate 20, and the like.
• the present compositions may also contain minor amounts of wetting or emulsifying agents, or pH buffering agents.
• the pharmaceutical formulations of the present disclosure are prepared by methods well-known in pharmaceutics.
• one or more accessory ingredients e.g., buffers, flavoring agents, surface active agents, and the like
• the choice of carrier is determined by the solubility and chemical nature of the compounds, chosen route of administration and standard pharmaceutical practice.
• the composition is in unit dose form such as a tablet, capsule or single-dose vial.
• Suitable unit doses i.e., therapeutically effective amounts, may be determined during clinical trials designed appropriately for each of the conditions for which administration of a chosen compound is indicated and will, of course, vary depending on the desired clinical endpoint.
• any of the compounds and/or compositions of the disclosure may be provided in a kit comprising the compounds and/or compositions.
• the compound and/or composition of the disclosure is provided in a kit comprising in the same package or separate package, a carrier and optionally instructions for using the kit for therapeutic or prophylactic end usage.
• the methods described herein include the administration of an AR inhibitor and one more additional therapeutic agents.
• the additional therapeutic agents may be administered before, concurrently with or after the AR inhibitor, but in a manner that provides for overlap of the pharmacological activity of the AR inhibitor and the additional therapeutic agent.
• the additional therapeutic agent can be, for example, second aldose reductase inhibitor, an antioxidant, or both.
• the 2 nd aldose reductase can be a compound described in, for example, in U.S. Patent Nos. 5,677,342; 5,155,259; 4,939,140; US US2006/0293265; and Roy et al. (Diabetes Research and Clinical Practice, 10, Issue 1, 91 -97, 1990; and references cited therein; each of which hereby incorporated by reference in its entirety.
• Aldose reductase inhibitors include, for example, zopolrestat, epalrestat, ranirestat, berberine and sorbinil, as described in, e.g., U.S. Patent No. 4,939,140; 6,159,976; and 6,570,013.
• the 2 nd aldose reductase inhibitor is selected from ponalrestat, epalrestat, sorbinil or sorbinol, imirestat, AND-138, CT-112, zopolrestat, zenarestat, BAL-AR18, AD-5467, M-79175, tolrestat, alconil, statil, berberine or SPR-210.
• Other therapeutic agents that can be administered include, for example corticosteroids, e.g., prednisone, methylprednisolone, dexamethasone, or triamcinalone acetinide, or noncorticosteroid anti-inflammatory compounds, such as ibuprofen or flubiproben,.
• corticosteroids e.g., prednisone, methylprednisolone, dexamethasone, or triamcinalone acetinide
• noncorticosteroid anti-inflammatory compounds such as ibuprofen or flubiproben
• vitamins and minerals e.g., zinc, and micronutrients can be coadministered.
• inhibitors of the protein tyrosine kinase pathway which include natural protein tyrosine kinase inhibitors like quercetin, lavendustin A, erbstatin and herbimycin A, and synthetic protein tyrosine kinase inhibitors like tyrphostins (e.g., AG490, AG17, AG213 (RG50864), AG18, AG82, AG494, AG825, AG879, AG1112, AG1296, AG1478, AG126, RG13022, RG14620 and AG555), dihydroxy-and dimethoxybenzylidene malononitrile, analogs of lavendustin A (e.g., AG814 and AG957), quinazolines (e.g., AG1478), 4,5-dianilinophthalimides, and thiazolidinediones, can be co-administered with genistein or an analog, prodrug or pharmaceutically acceptable salt thereof (see Levi
• potentially useful derivatives of genistein include those set forth in Mazurek et ah, U. S. Patent No. 5,637,703.
• Selenoindoles (2-thioindoles) and related disulfide selenides, such as those described in Dobrusin et ah, U. S. Patent No. 5,464,961, are useful protein tyrosine kinase inhibitors.
• Neutralizing proteins to growth factors such as a monoclonal antibody that is specific for a given growth factor, e.g., VEGF (for an example, see Aiello et ah, PNAS USA 92: 10457-10461 (1995)), or phosphotyrosine (Dhar et ah, Mol. Pharmacol. 37: 519-525 (1990)), can be co-administered.
• VEGF for an example, see Aiello et ah, PNAS USA 92: 10457-10461 (1995)
• phosphotyrosine Dhar et ah, Mol. Pharmacol. 37: 519-525 (1990)
• Other various compounds that can be co-administered include inhibitors of protein kinase C (see, e.g., U. S. Patent Nos.
• cytokine modulators an endothelial cell-specific inhibitor of proliferation, e.g., thrombospondins, an endothelial cell-specific inhibitory growth factor, e.g., TNFa, an anti-proliferative peptide, e.g., SPARC and prolferin-like peptides, a glutamate receptor antagonist, aminoguanidine, an angiotensin-converting enzyme inhibitor, e.g., angiotensin II, calcium channel blockers, y-tectorigenin, ST638, somatostatin analogues, e.g., SMS 201-995, monosialoganglioside GM1, ticlopidine, neurotrophic growth factors, methyl-2,5-dihydroxycinnamate, an angiogenesis inhibitor, e.g., recombinant EPO, a sulphonylurea oral hypoglycemic agent, e
• the disclosure further relates to diagnosing or prognosticating the risk of developing galactosemia in a subject by measuring one or more biomarkers associated with galactosemia.
• the biomarker associated with galactosemia is increased galactitol levels in a biological sample obtained from a subject.
• Diagnosis may be performed, e.g., by detecting elevated levels of sugar metabolites, e.g., metabolites of galactose ⁇ e.g., galactitol) and/or glucose ⁇ e.g., sorbitol) in the biological sample, e.g., aqueous or vitreous humor of the eye, blood tissue, cerebrospinal fluid, urine, etc.
• Tables 1 and 2 show concentrations of galactose and metabolites thereof in plasma (or whole blood), erythrocyte, and/or urine samples of subjects with classic galactosemia (GALT deficiency) or severe GALK deficiency.
• the disclosure further relates to methods for combined diagnosis and intervention of galactosemia, wherein, diagnosis of galactosemia is carried out as described previously via detection of one or more biomarkers in a sample obtained from the subject. Based on the results of the diagnosis, if the subject is determined to have or deemed to be at risk of developing galactosemia, then a composition comprising an aldose reductase inhibitor (ARI) is administered to the subject.
• the ARI comprises a compound of the instant disclosure or a composition comprising the compound of the instant disclosure.
• the present disclosure provides a method for treating galactosemia, comprising diagnosing a subject for galactosemia by detecting elevated plasma galactitol concentration (e.g., >10 ⁇ galactitol) and/or elevated urinary galactitol levels (e.g., >100 mmol galactitol/mol of creatine); and administering to the galactosemic subject in need thereof, an therapeutically effective amount of a composition that inhibits aldose reductase activity.
• elevated plasma galactitol concentration e.g., >10 ⁇ galactitol
• urinary galactitol levels e.g., >100 mmol galactitol/mol of creatine
• the diagnosis step may further comprise a genetic test, e.g., detecting a mutation in one or more of the enzymes involved in Leloir pathway (e.g., GALT, GALK, GALE, etc.).
• the diagnosis step may additionally comprise conducting an enzymatic assay, e.g., an assay for GALT, GALK, and/or GALE activity using detectable substrates, the products of which may be detected using routine methods, e.g., HPLC or mass spectrometry (Ko et ah, Clinical Chemistry 56:5 764-771, 2010).
• the present disclosure further provides for the use of the compounds of Formula I-VI, or a pharmaceutically acceptable salt, hydrate, solvate, or prodrug thereof, in a method of treating a disease state, and/or condition caused by or related to galactosemia.
• the disclosure relates to use of the compounds of Formula I-VI, or a pharmaceutically acceptable salt, hydrate, solvate, or prodrug thereof, in a method of treating a disease state, and/or condition caused by or related to galactosemia, comprising the steps of: (a) identifying a subject in need of such treatment; (b) providing a compound of Formula I- VI, or a pharmaceutically acceptable salt, hydrate, solvate, prodrug thereof; and (c) administering said compound of Formula I-VI in a therapeutically effective amount to treat, suppress and/or prevent the disease state or condition in a subject in need of such treatment.
• the disclosure relates to use of the compounds of Formula I- VI, or a pharmaceutically acceptable salt, hydrate, solvate, or prodrug thereof, in a method of treating a disease state, and/or condition caused by or related to galactosemia, comprising the steps of: (a) identifying a subject in need of such treatment; (ii) providing a composition comprising a compound of Formula I-VI, or a pharmaceutically acceptable salt, hydrate, solvate, prodrug or tautomer thereof; and (iii) administering said composition in a therapeutically effective amount to treat, suppress and/or prevent the disease state or condition in a subject in need of such treatment.
• the compound or composition is preferably used orally.
• the rats will be fed a diet containing one or more aldose reductase inhibitors (ARIs), and the effect of AR inhibition will be assayed at the tissue level and also at the in vivo level.
• ARIs aldose reductase inhibitors
• galactitol levels in the eye of GALT-deficient rats may be measured pre- and post-treatment with the ARIs disclosed herein.
• the effect of ARIs in reducing the frequency and severity of galactosemia and/or improving the outcome of the disease e.g., improved visual, motor or memory skills
• ARI aldose reductase inhibitors
• BID 12-hour intervals
• drug was stored at -20°C in a bottle or tubes wrapped in aluminum foil.
• an aliquot of drug was re-suspended in formula, mixed well, and pipetted into individual tubes to be fed to the pups (volume calculated per pup weight measured that morning). All placebo and drug tubes of formula were warmed to 37°C immediately before feeding.
• Placebo and drug were fed to pups by hand using a syringe and tubing.
• Pups receiving drug also were fed a small additional volume of Gerber formula that had been used to wash the tube and syringe immediately after the drug feeding.
• pups were removed from their mother (to prevent nursing) and maintained in nests in a humidified incubator for about 2 hours at 35-37°C prior to each feeding. Separate syringes were used for placebo and drug.
• Pups were wrapped in fleece during feeding, which lasted about 2-5 minutes each.
• Pup GALT genotypes (M3/M3 versus M3/+ versus +/+) were determined by Transnetyx using DNA isolated from tail snips collected from all pups at between 5-8 days after birth. Genotypes were corroborated in representative pups by GALT enzyme activity measured in liver samples harvested from pups after euthanasia. In all samples tested, the GALT activity observed was consistent with the GALT genotype.
• Euthanizing pups Pups were euthanized by CC inhalation according to standard procedures.
• Enzyme assays Galactose-l-P uridylyltransferase (GALT) and galactokinase (GALK) assays were performed as described previously (Sanders et al, Dis Model Mech., 3(9-10):628-38, 2010) using lysates prepared from frozen samples of liver. GALK assays were performed as a control for integrity of the samples. Lysates were prepared by homogenizing small pieces (10-50 mg) of liver in 100 ⁇ of lysis buffer consisting of one complete mini protease inhibitor cocktail tablet, EDTA-free (Roche, REF 04 693 159 001) dissolved in 10 ml of 100 mM glycine, pH 8.7.
• the lysates were centrifuged at 16,110 X g for 5 mins at 4°C, and the resulting supernatant was passed over a MICRO BIO-SPIN P-6 chromatography column (Bio-Rad, Inc.) to remove small molecules. Protein concentrations were determined for each sample using the BIO-RAD DC protein assay with BSA as the standard. GALT and GALK assays were run using 4 ⁇ g of total protein per reaction. Substrates and products were quantified by HPLC as described previously (Ross, 2004).
• Metabolites Lysates for metabolite analysis were prepared as follows: 50-100 mg pieces of previously frozen liver or brain were homogenized by grinding for 30 seconds using a Teflon micropestle and handheld micropestle motor (Kimble Chase Life Science and Research Products LLC) in 125 ⁇ ice-cold HPLC-grade water. Metabolites were separated and quantified by HPLC (See, e.g., Daenzer, et al. Dis. Model Mech. 2016, 9(11): 1375- 1382)). Galactitol, inositol, and glucose were quantified using the same HPLC conditions described to quantify galactose by (Daenzer, 2016).
• Metabolite levels were normalized to the total area of peaks detected by the relevant column and elution run for that sample, minus the peaks that most distinguished homozygous M3/M3 samples from controls. Specifically, metabolites separated on the MAI column (galactitol, inositol, galactose and glucose) were normalized to total peak area minus galactose and galactitol, and metabolites separated on the PA10 column (galactose- IP) were normalized to total peak area minus galactose and galactose- IP.
• Cataracts are the most obvious and visible phenotype associated with GALT-null status in the rat model.
• the rats open their eyes at day 14 of life with bilateral cataracts present.
• infants with classic galactosemia exposed to dietary galactose e.g., breast milk
• cataracts are seen in all M3/M3 homozygous pups but not in any M3/+ or +/+ pups.
• cataracts were qualitatively assessed in GALT null rats that were treated with Compound A or placebo at day nine of life.
• Metabolites Galactose and galactitol metabolites were resolved and quantified via HPLC in samples of both liver and brain from euthanized pups. Treatment with Compound A reduced liver galactitol levels by 87% compared to placebo in GALT null rats at day 9 and by 57% at day 15-18. Treatment with Compound A reduced brain galactitol levels by 40% compared to placebo in GALT null rats at day 9 and by 57% at day 15-18. Additional studies were conducted in rats treating using Compound B, and galactose and galactitol levels were measured at day 10 of life. The results of this study showed that GALT null rats had elevated levels of galactitol in the liver, brain and plasma in comparison to wild type rats.
• Treatment with Compound B reduced galactitol levels in GALT null rats to normal or near normal levels.
• FIG. 3A The GALT null rats also had elevated galactose and GallP levels, relative to wild type rats. Treatment with Compound B did not further increase the galactose or GallP levels in the GALT null rats.
• FIG. 3B, and FIG. 3C The data demonstrate that aldose reductase inhibitors can reduce and normalize galactitol levels in affected animals, but does not further elevate galactose and GallP levels.
• GALT null rats In this study longer-term cognitive and neurological deficiencies associated with galactosemia will be studied in GALT null rats and normal control rats that are treated with placebo or with aldose reductase inhibitor.
• the aldose reductase inhibitors will be administered substantially as described in Example 1, and rats will be evaluated for central nervous system outcomes using rotarod testing, to assess balance, motor control and learning, as well as using novel object recognition testing, to assess cognition and memory.
• GALT null rats show altered responses in these tests in comparison to wild type rats. The data will show that treatment with aldose reductase inhibitor decreased cognitive and neurological deficiencies of GALT null rats, and that some or all responses of GALT null rats were normalized to the responses observed in wild type rats.
• a newborn child is diagnosed with classical galactosemia by neonatal testing and presents with elevated blood galactose and galactitol levels.
• the child is immediately place on a galactose and lactose restricted diet.
• Therapy with an aldose reductase inhibitor (such as Compound A or Compound B) is initiated at a dose selected by the clinician to normalize blood galactose and/or galactitol levels.
• Treatment results in reduction and eventual normalization of blood galactitol levels.
• the child continues therapy indefinitely and periodic checks confirm that blood galactitol levels remain normal. Dosing is adjusted as needed to maintain normal blood galactitol levels.
• the child does not exhibit growth delay, delayed speech, impaired learning, motor ataxia or presenile cataracts as she ages.
• An adult patient with galactosemia presents with motor ataxia, spasticity and poor balance.
• Therapy with an aldose reductase inhibitor (such as Compound A or Compound B) is initiated at a dose selected by the clinician to normalize blood galactose and/or galactitol levels.
• Treatment results in reduction and eventual normalization of blood galactitol levels.
• galactitol levels normalize, the patient exhibits decreased motor ataxia and spasticity, and improved balance. Dosing is adjusted as needed to maintain normal blood galactitol levels, and improvements in the patient's motor control and balance.

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