IP Library Granted Patent US 11,207,327
Granted Patent B2
US 11,207,327 · App. 17/145,744 · Granted Dec 28, 2021

Pharmaceutical compositions comprising meloxicam

Inventor: Herriot Tabuteau (New York, NY)
Assignee: AXSOME THERAPEUTICS, INC.
A61K31/5415A61K9/20A61K31/4196A61K33/10A61K47/6951A61P25/06A61K31/721A61P29/00
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Quick Facts
Patent No.
US 11,207,327
App. No.
17/145,744
Filed
Jan 11, 2021
Granted
Dec 28, 2021
Kind
B2
Art Unit
1628
USPC
514/226.5
Abstract

Disclosed herein are compositions comprising an NSAID such as meloxicam and/or rizatriptan in combination with a cyclodextrin and/or a carbonate or a bicarbonate. These compositions may be orally administered, for example, to improve the bioavailability or pharmacokinetics of the NSAID for the treatment of pain such as migraine, arthritis, and other conditions. Also disclosed herein are methods of treating pain, such as migraine, comprising administering meloxicam and rizatriptan to a human being suffering from pain, such as migraine. For migraine, these methods may be particularly useful when the meloxicam and rizatriptan are administered while the human being is suffering from an acute attack of migraine pain or migraine aura. In some embodiments, the combination of meloxicam and rizatriptan may be administered in a manner that results in a T max of meloxicam of 3 hours or less.

Claims (21)

1. A method of relieving migraine pain, comprising: orally administering to a human being in need thereof, a combination of: 1) a complex of a meloxicam and a sulfobutylether-β-cyclodextrin, 2) a bicarbonate, and 3) a rizatriptan, wherein the combination is orally administered when the human being is suffering from moderate to severe migraine pain of an acute migraine, and wherein one hour after the combination is orally administered, the human being experiences a greater reduction in migraine pain than the human being would experience one hour after the same amount of the rizatriptan is orally administered alone.

2. The method of claim 1 , wherein two hours after the combination is orally administered, the human being experiences a greater reduction in migraine pain than the human being would experience two hours after the same amount of the rizatriptan is orally administered alone.

3. The method of claim 1 , wherein two hours after the combination is orally administered, the human being experiences a greater reduction in the human being's most bothersome symptom than the human being would experience two hours after the same amount of the rizatriptan is orally administered alone, and wherein the most bothersome symptom is nausea, phonophobia, or photophobia.

4. The method of claim 1 , wherein twenty four hours after the combination is orally administered, the human being experiences a greater reduction in migraine pain than the human being would experience twenty four hours after the same amount of the rizatriptan is orally administered alone.

5. The method of claim 1 , wherein 1) the complex of the meloxicam and the sulfobutylether-β-cyclodextrin, 2) the bicarbonate, and 3) the rizatriptan, are combined together in a monolayer tablet.

6. The method of claim 1 , wherein the combination contains: about 10 mg of rizatriptan in the free base form or a molar equivalent of a salt form; about 20 mg of meloxicam in the free base form, or a molar equivalent of a salt form; and about 400 mg to about 600 mg of the bicarbonate.

7. The method of claim 6 , wherein the bicarbonate is sodium bicarbonate.

8. The method of claim 6 , wherein thirty minutes after the combination is orally administered, the human being experiences a greater reduction in migraine pain than the human being would experience thirty minutes after the same amount of the rizatriptan is orally administered alone.

9. The method of claim 8 , wherein 1) the complex of the meloxicam and the sulfobutylether-β-cyclodextrin, 2) the bicarbonate, and 3) the rizatriptan, are combined together in a monolayer tablet.

10. The method of claim 8 , wherein twenty four hours after the combination is orally administered, the human being experiences a greater reduction in migraine pain than the human being would experience twenty four hours after the same amount of the rizatriptan is orally administered alone.

11. The method of claim 1 , wherein the human being achieves pain freedom one hour after the combination is orally administered.

12. The method of claim 1 , wherein the human being achieves absence of the most bothersome symptom to the human being two hours after the combination is orally administered, and wherein the most bothersome symptom is nausea, phonophobia, or photophobia.

13. The method of claim 1 , wherein the complex of the meloxicam and the sulfobutylether-β-cyclodextrin are present in a dosage form with the bicarbonate, and the bicarbonate is present in an amount that is effective to increase the dissolution rate of meloxicam.

14. The method of claim 1 , wherein the human being has migraine pain that is accompanied with nausea.

15. The method of claim 14 , wherein two hours after the combination is orally administered, the human being experiences a greater reduction in nausea than the human being would experience two hours after the same amount of the rizatriptan is orally administered alone.

16. The method of claim 1 , wherein the bicarbonate is sodium bicarbonate.

17. The method of claim 1 , wherein the meloxicam is in the free base form.

18. The method of claim 1 , wherein the rizatriptan is rizatriptan benzoate.

19. The method of claim 1 , wherein the complex of the meloxicam and the sulfobutylether-β-cyclodextrin, the bicarbonate, and the rizatriptan are present in a single dosage form.

20. The method of claim 1 , wherein migraine pain is accompanied by disturbed vision.

21. The method of claim 20 , wherein the human being achieves absence of the disturbed vision two hours after the combination is orally administered.

Assignments (2)
SECURITY INTEREST Recorded May 9, 2025
From: AXSOME THERAPEUTICS, INC.; AXSOME MALTA LTD.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 071247/0836 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 17, 2021
From: TABUTEAU, HERRIOT
To: AXSOME THERAPEUTICS, INC.
Reel/Frame 056259/0713 →
Continuity (12)
Continuation In Part 16854320 · Apr 21, 2020
Continuation In Part 16570451 · Sep 13, 2019
Continuation In Part 16001697 · Jun 6, 2018
Continuation In Part 15976800 · May 10, 2018
Continuation In Part PCTUS2018012433 · Jan 4, 2018
Provisional Application 62504105 · May 10, 2017
Provisional Application 62536466 · Jul 25, 2017
Provisional Application 62442136 · Jan 4, 2017
Provisional Application 62504105 · May 10, 2017
Provisional Application 62536466 · Jul 25, 2017
Provisional Application 62680956 · Jun 5, 2018
Related Publication 20210128575A1 · May 6, 2021
Cited By (16)
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