IP Library Patent Application 19195620
Patent Application
App. No. 19/195,620

COMBINATION DOSAGE FORMS AND ADMINISTRATION THEREOF

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Quick Facts
Patent No.
US None
App. No.
19/195,620
Abstract

This disclosure relates to methods of administering bupropion, such as S-bupropion or R-bupropion, in conjunction with tetrabenazine, alpha-dihydrotetrabenazine, or beta-dihydrotetrabenazine to a human being. Dosage forms, drug delivery systems, and methods related to tetrabenazine, alpha-dihydrotetrabenazine, or beta-dihydrotetrabenazine and bupropion, such as S-bupropion or R-bupropion, are also disclosed.

Claims (16)

1 - 24 . (canceled)

25 . A dosage form, comprising from about 5 mg to about 30 mg of a tetrabenazine or a pharmaceutically acceptable salt thereof and bupropion hydrochloride, wherein the dosage form is a solid or a liquid dosage form, and wherein the tetrabenazine is not deuterium-modified.

26 . The dosage form of claim 25 , wherein the dosage form is a solid dosage form.

27 . The dosage form of claim 25 , comprising from about 70 mg to about 140 mg of the bupropion hydrochloride.

28 . The dosage form of claim 25 , comprising from about 10 mg to about 15 mg of the tetrabenazine or a pharmaceutically acceptable salt thereof.

29 . The dosage form of claim 28 , comprising from about 90 mg to about 110 mg of the bupropion hydrochloride.

30 . The dosage form of claim 25 , comprising from about 90 mg to about 110 mg of the bupropion hydrochloride.

31 . The dosage form of claim 25 , wherein the bupropion hydrochloride comprises (S)-bupropion hydrochloride.

32 . The dosage form of claim 31 , wherein the (S)-bupropion hydrochloride has an enantiomeric excess of at least 97%.

33 . The dosage form of claim 25 , comprising from about 70 mg to about 100 mg of the bupropion hydrochloride.

34 . The dosage form of claim 25 , comprising from about 100 mg to about 140 mg of the bupropion hydrochloride.

35 . The dosage form of claim 25 , comprising from about 9 mg to about 12 mg of the tetrabenazine or a pharmaceutically acceptable salt thereof.

36 . The dosage form of claim 25 , comprising from about 12 mg to about 15 mg of the tetrabenazine or a pharmaceutically acceptable salt thereof.

37 . The dosage form of claim 25 , wherein the bupropion hydrochloride is not deuterium-modified.

38 . The dosage form of claim 25 , wherein the bupropion hydrochloride comprises from about 70 mg to about 140 mg of (S)-bupropion hydrochloride.

39 . The dosage form of claim 38 , wherein the (S)-bupropion hydrochloride is not deuterium-modified.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 21, 2025
From: TABUTEAU, HERRIOT
To: AXSOME THERAPEUTICS, INC.
Reel/Frame 072360/0140 →