IP Library Patent Application 18056848
Patent Application
App. No. 18/056,848

COMPOUNDS AND COMBINATIONS THEREOF FOR TREATING NEUROLOGICAL AND PSYCHIATRIC CONDITIONS

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Quick Facts
Patent No.
US None
App. No.
18/056,848
Abstract

Dosage forms, drug delivery systems, and methods related to sustained release of dextromethorphan or improved therapeutic effects are disclosed. Typically, an antidepressant, such as bupropion or a related compound is orally administered to a human being to be treated with, or being treated with, dextromethorphan.

Claims (18)

1 . A method of treating depression comprising: orally administering a dosage form to a human being in need thereof for at least 8 consecutive days, wherein the dosage form comprises a dextromethorphan and a fluoxetine, wherein the human being receives a total daily dose of about 30 mg to about 150 mg of the dextromethorphan; wherein the dextromethorphan and the fluoxetine are the only therapeutically active agents in the dosage form; wherein the human being is an extensive metabolizer of dextromethorphan; wherein on day 8, the human being has a dextromethorphan/dextrorphan plasma ratio of 0.3 or greater three hours after the dosage form is administered.

2 . The method of claim 1 , wherein the dosage form comprises about 20 mg to about 50 mg of the fluoxetine.

3 . The method of claim 1 , wherein the depression is major depressive disorder.

4 . The method of claim 1 , wherein the depression is treatment resistant depression.

5 . The method of claim 1 , wherein the dosage form is orally administered for at least 14 consecutive days.

6 . The method of claim 1 , wherein the dosage form provides immediate release of the dextromethorphan.

7 . The method of claim 1 , wherein the dosage form contains about 20 mg to about 50 mg of the dextromethorphan.

8 . The method of claim 1 , wherein the dosage form contains about 30 mg to about 60 mg of the dextromethorphan.

9 . The method of claim 1 , wherein the dosage form contains about 40 mg to about 50 mg of the dextromethorphan.

10 . The method of claim 1 , wherein the dosage form contains about 50 mg to about 70 mg of the dextromethorphan.

11 . The method of claim 1 , wherein the dosage form contains about 70 mg to about 100 mg of the dextromethorphan.

12 . The method of claim 1 , wherein the dosage form contains about 45 mg of a dextromethorphan salt.

13 . The method of claim 1 , wherein the dextromethorphan comprises a deuterium-modified dextromethorphan.

14 . The method of claim 1 , wherein the dosage form is a capsule, a tablet, or a solution.

15 . The method of claim 1 , wherein a dextromethorphan plasma level is increased as compared to administering the same amount of dextromethorphan alone.

16 . The method of claim 1 , wherein the human being is converted to a poor metabolizer of dextromethorphan.

17 . The method of claim 1 , wherein the dosage form further comprises a pharmaceutically acceptable excipient.

18 . The method of claim 1 , wherein the elimination half-life of dextromethorphan increases upon administration of the dosage form.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 6, 2023
From: TABUTEAU, HERRIOT
To: ANTECIP BIOVENTURES II LLC
Reel/Frame 062296/0621 →