IP Library Granted Patent US 10,137,131
Granted Patent B2
US 10,137,131 · App. 15/936,176 · Granted Nov 27, 2018

Pharmaceutical compositions comprising meloxicam

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Quick Facts
Patent No.
US 10,137,131
App. No.
15/936,176
Granted
Nov 27, 2018
Kind
B2
Abstract

Disclosed herein are compositions comprising a drug such as a triptan (e.g. rizatriptan) and/or an NSAID (e.g. 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 drug for the treatment of conditions such as pain.

Claims (29)

1. A dosage form comprising a combination of: 1) a complex of meloxicam with a sulfobutyl ether β-cyclodextrin (SBEβCD), 2) a bicarbonate, and 3) a triptan; wherein the dosage form contains 400 mg to 600 mg of the bicarbonate, about 5 mg to about 50 mg of meloxicam, and about 50 mg to about 200 mg of SBEβCD; and wherein the dosage form is a solid oral dosage form having a shorter T max of meloxicam in a human being than a reference dosage form that: 1) contains the same amount of meloxicam, 2) does not contain an SBEβCD, and 3) does not contain a bicarbonate.

2. The dosage form of claim 1 , wherein the triptan is a rizatriptan.

3. The dosage form of claim 2 , wherein about 8 mg to about 13 mg of the rizatriptan is present in the dosage form based upon the weight of the rizatriptan in the free base form.

4. The dosage form of claim 3 , wherein the rizatriptan is present in a salt form in an amount that is a molar equivalent of about 10 mg of the rizatriptan in the free base form.

5. The dosage form of claim 4 , wherein the rizatriptan is present as rizatriptan benzoate.

6. The dosage form of claim 1 , containing about 15 mg to about 25 mg of meloxicam.

7. The dosage form of claim 1 , containing about 20 mg of meloxicam.

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

9. The dosage form of claim 1 , containing about 100 mg to about 175 mg of the SBEβCD.

10. The dosage form of claim 1 , containing about 100 mg to about 140 mg of SBEβCD.

11. The dosage form of claim 1 , wherein the bicarbonate comprises sodium bicarbonate.

12. The dosage form of claim 11 , containing about 500 mg of sodium bicarbonate.

13. The dosage form of claim 1 , wherein the oral dosage form has been shown to have a median T max of meloxicam that is less than about 3 hours in fasted human subjects.

14. The dosage form of claim 1 , wherein the oral dosage form has been shown to have a median T max of meloxicam that is less than about 2 hours in fasted human subjects.

15. The dosage form of claim 1 , wherein the oral dosage form has been shown to have a median T max of meloxicam that is less than about 1 hour in fasted human subjects.

16. The dosage form of claim 1 , wherein the oral dosage form has been shown to have a median C max of meloxicam that is at least 1800 ng/mL in fasted human subjects.

17. The dosage form of claim 1 , wherein the oral dosage form has been shown to have a median AUC 0-6 of meloxicam that is at least 6,000 ng·hr/mL in fasted human subjects.

18. The dosage form of claim 1 , wherein the oral dosage form has been shown to have a median time to half-maximal plasma concentration of meloxicam that is less than about 30 minutes in fasted human subjects.

19. A method of treating migraine, comprising administering a dosage form of claim 1 to a human being in need thereof.

20. The method of claim 19 , wherein the oral dosage form has been shown to have a median T max of meloxicam that is less than about 1 hour in fasted human subjects.

21. The method of claim 19 , wherein the oral dosage form has been shown to have a median C max of meloxicam that is at least 1800 ng/mL in fasted human subjects.

22. The method of claim 19 , wherein the oral dosage form has been shown to have a median AUC 0-6 of meloxicam that is at least 6,000 ng·hr/mL in fasted human subjects.

23. The method of claim 19 , wherein the oral dosage form has been shown to have a median time to half-maximal plasma concentration of meloxicam that is less than about 30 minutes in fasted human subjects.

24. The method of claim 19 , wherein the triptan is a rizatriptan.

25. The method of claim 24 , wherein about 5 mg to about 20 mg of the rizatriptan is present in the dosage form based upon the weight of the rizatriptan in the free base form.

26. The method of claim 25 , wherein the rizatriptan is present in a salt form in an amount that is a molar equivalent of about 10 mg of the rizatriptan in the free base form.

27. The method of claim 26 , wherein the rizatriptan is present as rizatriptan benzoate.

28. The method of claim 19 , wherein the dosage form contains about 10 mg to about 30 mg of meloxicam.

29. The method of claim 19 , wherein the dosage form contains about 20 mg of meloxicam.

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 21, 2018
From: TABUTEAU, HERRIOT
To: AXSOME THERAPEUTICS, INC.
Reel/Frame 045865/0404 →