IP Library Patent Application 19278734
Patent Application
App. No. 19/278,734

BUPROPION AS A MODULATOR OF DRUG ACTIVITY

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Quick Facts
Patent No.
US None
App. No.
19/278,734
Abstract

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

Claims (20)

1 . A method of treating depression comprising: orally administering a dosage form once a day or twice a day to a human being suffering from depression; wherein the dosage form comprises dextromethorphan or a pharmaceutically acceptable salt thereof, and citalopram or a pharmaceutically acceptable salt thereof; wherein the dextromethorphan and the citalopram are the only therapeutically active agents in the dosage form; and wherein the human being is an extensive metabolizer of dextromethorphan.

2 . The method of claim 1 , wherein the dosage form is orally administered for at least 8 consecutive days.

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 comprises about 10 mg to about 20 mg of the citalopram.

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

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

8 . The method of claim 1 , wherein the dosage form provides sustained release of the citalopram.

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

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

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

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

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

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

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

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

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

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

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

20 . The method of claim 1 , wherein the elimination half-life of dextromethorphan increases upon orally administering the dosage form.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 22, 2025
From: TABUTEAU, HERRIOT
To: ANTECIP BIOVENTURES II LLC
Reel/Frame 072100/0380 →