Enantiomerically pure S-etifoxine, pharmaceutical compositions thereof and methods of their use
View Patent ↗Enantiomerically pure S-etifoxine and pharmaceutically acceptable salts, solvates, hydrates or prodrugs thereof are provided. Also provided are pharmaceutical compositions comprising the compounds and methods of treating disorders associated with central nervous system using the compounds and pharmaceutical compositions.
1. Enantiomerically pure S-etifoxine, or a pharmaceutically acceptable salt thereof, wherein the enantiomerically pure S-etifoxine is at least 80% by weight S-etifoxine and at most 20% by weight R-etifoxine based on total weight of etifoxine.
2. The compound of claim 1 , wherein the compound is a salt.
3. The compound of claim 2 , wherein the salt is a hydrochloride salt.
4. A pharmaceutical composition comprising the compound claim 1 , or a pharmaceutically acceptable salt thereof, and a pharmaceutical carrier, excipient or diluent.
5. The pharmaceutical composition of claim 4 that is formulated for oral administration.
6. The pharmaceutical composition of claim 5 that is formulated as an oral capsule or a tablet.
7. The pharmaceutical composition of claim 4 that is formulated for topical administration.
8. The pharmaceutical composition of claim 7 that is formulated as a gel.
9. A pharmaceutical unit dosage comprising the pharmaceutical composition of claim 5 .
10. A method for modulating activity of GABA A receptor comprising contacting the receptor with an effective amount of the compound of claim 1 , or a pharmaceutically acceptable salt thereof.
11. The method of claim 10 wherein GABA A receptor comprising subunit β2 is selectively modulated relative to GABA A receptor comprising subunit β1.
12. A method of treating, ameliorating or managing symptoms associated with a disease comprising administering to a subject in need thereof an effective amount of a compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein the subject has a disease selected from anxiety, multiple sclerosis, muscle relaxation in spinal spasticity, cerebral palsy, trigeminal neuralgia, pain and drug withdrawal symptoms.
13. A method of treating, ameliorating or managing a gut motility disorder comprising administering to a subject having gut motility disorder an effective amount of a compound of claim 1 , or a pharmaceutically acceptable salt thereof.
14. A method of treating, ameliorating or managing anxiety comprising administering to a subject in need thereof an effective amount of a compound of claim 1 , or a pharmaceutically acceptable salt thereof.
15. The method of claim 10 , wherein the compound is administered as an oral or topical formulation.
16. The method of claim 15 , wherein the oral formulation is a capsule.
17. The method of claim 15 , wherein the topical formulation is a gel.
18. The method of claim 12 , wherein the amount of the compound administered is about 1 mg up to about 2000 mg/day.
19. The method of claim 12 , wherein the amount of the compound administered is about 10 mg up to about 1000 mg/day.
20. The method of claim 12 , wherein the amount of the compound administered is about 13 mg up to about 800 mg/day.
21. The method of claim 12 , wherein the amount of the compound administered is about 15 mg up to about 300 mg/day.
22. The method of claim 12 , wherein the amount of the compound administered is about 25 mg up to about 200 mg/day.
23. The method of claim 12 , wherein the amount of the compound administered is about 50 mg up to about 150 mg/day.
24. The method of claim 12 , wherein the amount of the compound administered is about 50 mg/day.
25. The method of claim 12 , wherein the amount of the compound administered is about 100 mg/day.
26. The method of claim 12 , wherein the amount of the compound administered is about 150 mg/day.
27. The method of claim 12 further comprising administering an additional anxiolytic drug to the patient.
28. The method of claim 27 , wherein the additional anxiolytic drug is selected from Buspirone, Gepirone, Ipsapirone, Tondospirone, Alprazolam, Bromazepam, Camazepam, Chlordiazepoxide, Clobazam, Clorazepate, Chotiazepam, Cloxazolam, Diazepam, Ethyl Loflazepate, Etizolam, Fluidazepam, Flutazolam, Flutoprazepam, Halazepam, Ketazolam, Lorazepam, Loxapine, Medazepam, Metaclazepam, Mexazolam, Nordazepam, Oxazepam, Oxazolam, Pinazepam, Prazepam, Tofisopam, Cyclarbamate, Emylcamate, Hydroxyphenamate, Meprobamate, Phenprobamate, Tybamate, Alpidem, Benzoctamine, Captodiamine, Chlormezanone, Flesinoxan, Fluoresone, Glutamic Acid, Hydroxyzine, Lesopitron, Mecloralurea, Mephenoxalone, Mirtazepine, Oxanamide, Phenaglycodol, Suriclone and Zatosetron.
29. The method of claim 12 wherein said administration causes reduced sedation in the subject compared to a comparable dose of racemic etifoxine.
30. The method of claim 14 , wherein the amount of the compound administered is about 1 mg up to about 2000 mg/day.
31. The method of claim 14 , wherein the amount of the compound administered is about 10 mg up to about 1000 mg/day.
32. The method of claim 14 , wherein the amount of the compound administered is about 13 mg up to about 800 mg/day.
33. The method of claim 14 , wherein the amount of the compound administered is about 15 mg up to about 300 mg/day.
34. The method of claim 14 , wherein the amount of the compound administered is about 25 mg up to about 200 mg/day.
35. The method of claim 14 , wherein the amount of the compound administered is about 50 mg up to about 150 mg/day.
36. The method of claim 14 , wherein the amount of the compound administered is about 50 mg/day.
37. The method of claim 14 , wherein the amount of the compound administered is about 100 mg/day.
38. The method of claim 14 , wherein the amount of the compound administered is about 150 mg/day.
39. The method of claim 14 further comprising administering an additional anxiolytic drug to the patient.
40. The method of claim 39 , wherein the additional anxiolytic drug is selected from Buspirone, Gepirone, Ipsapirone, Tondospirone, Alprazolam, Bromazepam, Camazepam, Chlordiazepoxide, Clobazam, Clorazepate, Chotiazepam, Cloxazolam, Diazepam, Ethyl Loflazepate, Etizolam, Fluidazepam, Flutazolam, Flutoprazepam, Halazepam, Ketazolam, Lorazepam, Loxapine, Medazepam, Metaclazepam, Mexazolam, Nordazepam, Oxazepam, Oxazolam, Pinazepam, Prazepam, Tofisopam, Cyclarbamate, Emylcamate, Hydroxyphenamate, Meprobamate, Phenprobamate, Tybamate, Alpidem, Benzoctamine, Captodiamine, Chlormezanone, Flesinoxan, fluoresone, Glutamic Acid, Hydroxyzine, Lesopitron, Mecloralurea, Mephenoxalone, Mirtazepine, Oxanamide, Phenaglycodol, Suriclone and Zatosetron.
41. The method of claim 14 , wherein said administration causes reduced sedation in the subject compared to a comparable dose of racemic etifoxine.
42. The method of claim 14 , wherein said administration causes reduced sedation in the subject compared to a comparable dose of racemic etifoxine.
43. The compound of claim 1 , wherein the enantiomerically pure S-etifoxine is at least 90% by weight S-etifoxine and at most 10% by weight R-etifoxine based on total weight of etifoxine.
44. The compound of claim 1 , wherein the enantiomerically pure S-etifoxine is at least 97% by weight S-etifoxine and at most 3% by weight R-etifoxine based on total weight of etifoxine.
45. The method of claim 12 , wherein the treatment is for anxiety and wherein the enantiomerically pure S-etifoxine is at least 97% by weight S-etifoxine and at most 3% by weight R-etifoxine based on total weight of etifoxine.
46. The method of claim 12 , wherein the treatment is for pain and wherein the enantiomerically pure S-etifoxine is at least 97% by weight S-etifoxine and at most 3% by weight R-etifoxine based on total weight of etifoxine.
47. The compound of claim 1 , wherein the pharmaceutically acceptable salt is selected from the group consisting of hydrochloric, hydrobromic, hydroiodic, nitric, sulfuric, and phosphoric.