IP Library Granted Patent US 10,195,279
Granted Patent B2
US 10,195,279 · App. 15/989,734 · Granted Feb 5, 2019

Pharmaceutical compositions comprising meloxicam

Inventor: Herriot Tabuteau (New York, NY)
Assignee: AXSOME THERAPEUTICS, INC.
A61K47/02A61K9/0053A61K9/2009A61K31/4439A61K31/5415A61K45/06A61K47/40A61K47/6951C08B37/0012C08B37/0015
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Quick Facts
Patent No.
US 10,195,279
App. No.
15/989,734
Granted
Feb 5, 2019
Kind
B2
Abstract

Disclosed herein are compositions comprising an NSAID such as meloxicam 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 conditions such as arthritis.

Claims (29)

1. A method of treating arthritis comprising: orally administering a solid dosage form to a human being suffering from arthritis, wherein the solid dosage form comprises: 1) a complex of meloxicam and a sulfobutyl ether β-cyclodextrin (SBEβCD), and 2) a bicarbonate, wherein orally administering the solid dosage form to the human being results in a T max of meloxicam that is shorter than a T max of a reference solid dosage form that: 1) contains the same amount of meloxicam, 2) does not contain an SBEβCD, and 3) does not contain a bicarbonate, wherein the solid dosage form has been shown to have a median T max of meloxicam that is less than 1 hour in human subjects.

2. The method of claim 1 , wherein the solid dosage form contains about 10 mg to about 20 mg of meloxicam.

3. The method of claim 1 , wherein the solid dosage form contains about 15 mg of meloxicam.

4. The method of claim 1 , wherein the SBEβCD has about 6 to about 7 sulfobutyl ether groups for each molecule of β-cyclodextrin.

5. The method of claim 1 , wherein the solid dosage form contains about 50 mg to about 200 mg of the SBEβCD.

6. The method of claim 1 , wherein the solid dosage form contains about 100 mg of the SBEβCD.

7. The method of claim 1 , wherein the solid dosage form contains about 400 mg to about 600 mg of the bicarbonate.

8. The method of claim 7 , wherein the solid dosage form contains about 500 mg of sodium bicarbonate.

9. The method of claim 1 , wherein the solid dosage form further comprises a proton pump inhibitor.

10. The method of claim 9 , wherein the proton pump inhibitor is esomeprazole.

11. The method of claim 10 , wherein about 30 mg to about 50 mg of esomeprazole is present in the solid dosage form.

12. The method of claim 11 , wherein the solid dosage form contains about 40 mg of esomeprazole.

13. The method of claim 1 , wherein the human being is suffering from osteoarthritis.

14. The method of claim 1 , wherein the human being is suffering from rheumatoid arthritis.

15. A method of treating arthritis comprising: orally administering a solid dosage form to a human being suffering from arthritis, wherein the solid dosage form comprises: 1) a complex of meloxicam and a sulfobutyl ether β-cyclodextrin (SBEβCD), and 2) a bicarbonate, wherein orally administering the solid dosage form to the human being results in a C max of meloxicam that is at least about 30% higher than a C max of a reference solid dosage form that: 1) contains the same amount of meloxicam, 2) does not contain an SBEβCD, and 3) does not contain a bicarbonate.

16. The method of claim 15 , wherein the solid dosage form contains about 10 mg to about 20 mg of meloxicam.

17. The method of claim 15 , wherein the solid dosage form contains about 15 mg of meloxicam.

18. The method of claim 15 , wherein the SBEβCD has about 6 to about 7 sulfobutyl ether groups for each molecule of β-cyclodextrin.

19. The method of claim 15 , wherein the solid dosage form contains about 50 mg to about 200 mg of the SBEβCD.

20. The method of claim 15 , wherein the solid dosage form contains about 100 mg of the SBEβCD.

21. The method of claim 15 , wherein the solid dosage form contains about 400 mg to about 600 mg of the bicarbonate.

22. The method of claim 21 , wherein the solid dosage form contains about 500 mg of sodium bicarbonate.

23. The method of claim 15 , wherein the solid dosage form further comprises an acid inhibitor.

24. The method of claim 23 , wherein the acid inhibitor is a proton pump inhibitor.

25. The method of claim 24 , wherein the proton pump inhibitor is esomeprazole.

26. The method of claim 25 , wherein about 30 mg to about 50 mg of esomeprazole is present in the solid dosage form.

27. The method of claim 26 , wherein the solid dosage form contains about 40 mg of esomeprazole.

28. The method of claim 15 , wherein the human being is suffering from osteoarthritis.

29. The method of claim 15 , wherein the human being is suffering from rheumatoid arthritis.

Assignments (4)
RELEASE OF SECURITY INTEREST Recorded May 22, 2025
From: HERCULES CAPITAL, INC.
To: AXSOME THERAPEUTICS, INC.
Reel/Frame 071337/0004 →
SECURITY INTEREST Recorded May 9, 2025
From: AXSOME THERAPEUTICS, INC.; AXSOME MALTA LTD.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 071247/0836 →
INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Sep 25, 2020
From: AXSOME THERAPEUTICS, INC.
To: HERCULES CAPITAL, INC., AS AGENT
Reel/Frame 053941/0491 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 29, 2018
From: TABUTEAU, HERRIOT
To: AXSOME THERAPEUTICS, INC.
Reel/Frame 045925/0767 →
Continuity (9)
Continuation 15902770 · Feb 22, 2018
Continuation 15797955 · Oct 30, 2017
Continuation In Part 15132130 · Apr 18, 2016
Continuation PCTUS2016026991 · Apr 11, 2016
Provisional Application 62114215 · Feb 10, 2015
Provisional Application 62259993 · Nov 25, 2015
Provisional Application 62526884 · Jun 29, 2017
Provisional Application 62536466 · Jul 25, 2017
Related Publication 20180271981A1 · Sep 27, 2018
Cited By (16)
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