IP Library Granted Patent US 11,298,351
Granted Patent B2
US 11,298,351 · App. 17/095,256 · Granted Apr 12, 2022

Bupropion as a modulator of drug activity

Inventor: Herriot Tabuteau (New York, NY)
Assignee: ANTECIP BIOVENTURES II LLC
A61K31/485A61K9/0053A61K31/135A61K31/137A61K31/15A61K31/343A61K31/381
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Quick Facts
Patent No.
US 11,298,351
App. No.
17/095,256
Granted
Apr 12, 2022
Kind
B2
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 (12)

1. A method of treating major depression, comprising: orally administering a dosage form once a day or twice a day for at least 7 days, to a human being suffering from major depression, wherein bupropion and dextromethorphan are the only therapeutically active compounds in the dosage form, wherein the human being receives a daily dose of the bupropion that is about 200 mg to about 250 mg, wherein the daily dose of the bupropion is orally administered once a day or is a total of two twice daily doses of the bupropion, wherein the human being receives a daily dose of the dextromethorphan that is about 60 mg to about 100 mg, wherein the daily dose of the dextromethorphan is orally administered once a day or is a total of two twice daily doses of the dextromethorphan, wherein orally administering the bupropion in combination with the dextromethorphan results in the human being experiencing a therapeutic effect; wherein the dosage form provides immediate release of dextromethorphan and sustained release of bupropion; and wherein orally administering the dosage form is more effective in treating major depression than orally administering the same amount of the dextromethorphan alone for the same number of consecutive days.

2. The method of claim 1 , wherein after orally administering the dosage form, the human being experiences an improvement in a depressive symptom as compared to baseline.

3. The method of claim 1 , wherein orally administering the dosage form is more effective in treating major depression than orally administering a placebo.

4. The method of claim 1 , wherein the dosage form is orally administered once daily.

5. The method of claim 1 , wherein the dosage form is orally administered twice daily.

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 is orally administered for at least 30 consecutive days.

8. The method of claim 1 , wherein the dosage form has a weight ratio of the dextromethorphan to the bupropion that is about 0.3 to about 0.5.

9. The method of claim 1 , wherein the dosage form is orally administered once a day for 1 day and twice a day thereafter.

10. The method of claim 1 , wherein the dosage form is orally administered once a day for 2 days and twice a day thereafter.

11. The method of claim 1 , wherein the dosage form is orally administered once a day for 3 days and twice a day thereafter.

12. The method of claim 1 , wherein orally administering the dosage form is more effective than orally administering a placebo in reducing anxiety.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 9, 2021
From: TABUTEAU, HERRIOT
To: ANTECIP BIOVENTURES II LLC
Reel/Frame 055189/0032 →