IP Library Granted Patent US 10,363,312
Granted Patent B2
US 10,363,312 · App. 16/248,449 · Granted Jul 30, 2019

Pharmaceutical compositions comprising meloxicam

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Quick Facts
Patent No.
US 10,363,312
App. No.
16/248,449
Granted
Jul 30, 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 pain.

Claims (30)

1. A method of treating migraine comprising: orally administering a solid dosage form once daily to a human being suffering from a migraine, 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 2 hours 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 bicarbonate is sodium bicarbonate.

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

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

10. The method of claim 1 , wherein the solid dosage form further comprises an acid inhibitor.

11. The method of claim 10 , wherein the acid inhibitor is a proton pump inhibitor.

12. The method of claim 11 , wherein the proton pump inhibitor is esomeprazole, and about 30 mg to about 50 mg of esomeprazole is present in the solid dosage form.

13. The method of claim 1 , wherein the dosage form further comprises rizatriptan.

14. The method of claim 1 , wherein the solid dosage form is administered once daily under fasting condition for about 1 to about 15 days.

15. The method of claim 1 , wherein the human being is being treated with another pain medication before the solid dosage form comprising meloxicam is orally administered, and wherein the use of another pain medication may be reduced by at least about 10% after administration of the solid dosage form.

16. A method of treating migraine comprising: orally administering a solid dosage form once daily to a human being suffering from a migraine, 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.

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

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

19. The method of claim 16 , wherein the SBEβCD has about 6 to about 7 sulfobutyl ether groups for each molecule of β-cyclodextrin.

20. The method of claim 16 , wherein the solid dosage form contains about 50 mg to about 200 mg of the SBEβCD.

21. The method of claim 16 , wherein the solid dosage form contains about 100 mg of the SBEβCD.

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

23. The method of claim 16 , wherein the solid dosage form contains about 400 mg to about 600 mg of the bicarbonate.

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

25. The method of claim 16 , wherein the solid dosage form further comprises an acid inhibitor.

26. The method of claim 25 , wherein the acid inhibitor is a proton pump inhibitor, and the proton pump inhibitor is esomeprazole.

27. The method of claim 16 , wherein the human being is being treated with another pain medication before the solid dosage form comprising meloxicam is orally administered, and wherein the use of another pain medication may be reduced by at least about 10% after administration of the solid dosage form.

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

29. The method of claim 16 , wherein the solid dosage form is administered once daily under fasting condition for about 1 to about 15 days.

30. The method of claim 16 , wherein the dosage form further comprises rizatriptan.

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 Mar 14, 2019
From: TABUTEAU, HERRIOT
To: AXSOME THERAPEUTICS, INC.
Reel/Frame 048598/0150 →