IP Library Granted Patent US 10,688,102
Granted Patent B2
US 10,688,102 · App. 16/513,612 · Granted Jun 23, 2020

Combination treatment for migraine and other pain

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,688,102
App. No.
16/513,612
Granted
Jun 23, 2020
Kind
B2
Abstract

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 (47)

1. A method of treating migraine, comprising administering a meloxicam and about 8 mg to about 13 mg of a rizatriptan, based upon the weight of the free base form of rizatriptan, to a human being who is suffering from an acute attack of migraine pain or migraine aura, wherein the meloxicam and the rizatriptan are administered within about 30 minutes of one another, wherein administering the meloxicam to the human being results in a T max of meloxicam of 110 minutes or less, and an AUC 0-24 of meloxicam of about 30 μg·hr/mL to about 50 μg·hr/mL, and wherein two hours after the meloxicam and the rizatriptan are administered, the human being experiences greater relief from nausea than the human being would have experienced two hours after receiving the same amount of the meloxicam without the rizatriptan.

2. The method of claim 1 , wherein the rizatriptan is administered in a salt form in an amount that is a molar equivalent to about 10 mg of the free base form of rizatriptan.

3. The method of claim 2 , wherein the rizatriptan is present as rizatriptan benzoate.

4. The method of claim 1 , wherein about 15 mg to about 25 mg of the meloxicam is administered to the human being.

5. The method of claim 1 , wherein about 20 mg of the meloxicam is administered to the human being.

6. The method of claim 1 , wherein the human being has a history of inadequate response to prior migraine treatments.

7. The method of claim 6 , wherein the rizatriptan is administered in a salt form in an amount that is a molar equivalent to about 10 mg of the free base form of rizatriptan.

8. The method of claim 6 , wherein about 15 mg to about 25 mg of the meloxicam is administered to the human being.

9. The method of claim 7 , wherein about 20 mg of the meloxicam is administered to the human being.

10. The method of claim 1 , wherein the meloxicam and the rizatriptan are administered simultaneously, and wherein two hours after the meloxicam and the rizatriptan are administered, the human being experiences greater pain relief than the human being would have experienced two hours after receiving the same amount of the meloxicam without the rizatriptan.

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

12. The method of claim 10 , wherein about 15 mg to about 25 mg of the meloxicam is administered to the human being.

13. The method of claim 11 , wherein about 20 mg of the meloxicam is administered to the human being.

14. The method of claim 1 , wherein the meloxicam and the rizatriptan are administered simultaneously, and wherein two hours after the meloxicam and the rizatriptan are administered, the human being experiences greater pain relief than the human being would have experienced two hours after receiving the same amount of the rizatriptan without the meloxicam.

15. The method of claim 14 , wherein the rizatriptan is administered in a salt form in an amount that is a molar equivalent to about 10 mg of the free base form of rizatriptan.

16. The method of claim 14 , wherein about 15 mg to about 25 mg of the meloxicam is administered to the human being.

17. The method of claim 15 , wherein about 20 mg of the meloxicam is administered to the human being.

18. The method of claim 1 , wherein the meloxicam and the rizatriptan are administered simultaneously, and wherein two hours after the meloxicam and the rizatriptan are administered, the human being experiences greater relief from nausea than the human being would have experienced two hours after receiving the same amount of the meloxicam without the rizatriptan.

19. A method of treating migraine, comprising administering a meloxicam and about 8 mg to about 13 mg of a rizatriptan, based upon the weight of the free base form of rizatriptan, to a human being who is suffering from an acute attack of migraine pain or migraine aura, wherein the meloxicam and the rizatriptan are administered within about 30 minutes of one another, wherein administering the meloxicam to the human being results in a T max of meloxicam of 110 minutes or less, and an AUC 0-24 of meloxicam of about 30 μg·hr/mL to about 50 μg·hr/mL, and wherein two hours after the meloxicam and the rizatriptan are administered, the human being experiences greater relief from nausea than the human being would have experienced two hours after receiving the same amount of the rizatriptan without the meloxicam.

20. A method of treating migraine, comprising administering a meloxicam and about 8 mg to about 13 mg of a rizatriptan, based upon the weight of the free base form of rizatriptan, to a human being who is suffering from an acute attack of migraine pain or migraine aura, wherein the meloxicam and the rizatriptan are administered within about 30 minutes of one another, wherein administering the meloxicam to the human being results in a T max of meloxicam of 110 minutes or less, and an AUC 0-24 of meloxicam of about 30 μg·hr/mL to about 50 μg·hr/mL, and wherein two hours after the meloxicam and the rizatriptan are administered, the human being experiences greater relief from vomiting than the human being would have experienced two hours after receiving the same amount of the meloxicam without the rizatriptan.

21. A method of treating migraine, comprising administering a meloxicam and about 8 mg to about 13 mg of a rizatriptan, based upon the weight of the free base form of rizatriptan, to a human being who is suffering from an acute attack of migraine pain or migraine aura, wherein the meloxicam and the rizatriptan are administered within about 30 minutes of one another, wherein administering the meloxicam to the human being results in a T max of meloxicam of 110 minutes or less, and an AUC 0-24 of meloxicam of about 30 μg·hr/mL to about 50 μg·hr/mL, and wherein two hours after the meloxicam and the rizatriptan are administered, the human being experiences greater relief from vomiting than the human being would have experienced two hours after receiving the same amount of the rizatriptan without the meloxicam.

22. A method of treating migraine, comprising administering a meloxicam and about 8 mg to about 13 mg of a rizatriptan, based upon the weight of the free base form of rizatriptan, to a human being who is suffering from an acute attack of migraine pain or migraine aura, wherein the meloxicam and the rizatriptan are administered within about 30 minutes of one another, wherein administering the meloxicam to the human being results in a T max of meloxicam of 110 minutes or less, and an AUC 0-24 of meloxicam of about 30 μg·hr/mL to about 50 μg·hr/mL, and wherein two hours after the meloxicam and the rizatriptan are administered, the human being experiences greater relief from photophobia than the human being would have experienced two hours after receiving the same amount of the meloxicam without the rizatriptan.

23. A method of treating migraine, comprising administering a meloxicam and about 8 mg to about 13 mg of a rizatriptan, based upon the weight of the free base form of rizatriptan, to a human being who is suffering from an acute attack of migraine pain or migraine aura, wherein the meloxicam and the rizatriptan are administered within about 30 minutes of one another, wherein administering the meloxicam to the human being results in a T max of meloxicam of 110 minutes or less, and an AUC 0-24 of meloxicam of about 30 μg·hr/mL to about 50 μg·hr/mL, and wherein two hours after the meloxicam and the rizatriptan are administered, the human being experiences greater relief from photophobia than the human being would have experienced two hours after receiving the same amount of the rizatriptan without the meloxicam.

24. A method of treating migraine, comprising administering a meloxicam and about 8 mg to about 13 mg of a rizatriptan, based upon the weight of the free base form of rizatriptan, to a human being who is suffering from an acute attack of migraine pain or migraine aura, wherein the meloxicam and the rizatriptan are administered within about 30 minutes of one another, wherein administering the meloxicam to the human being results in a T max of meloxicam of 110 minutes or less, and an AUC 0-24 of meloxicam of about 30 μg·hr/mL to about 50 μg·hr/mL, and wherein two hours after the meloxicam and the rizatriptan are administered, the human being experiences greater relief from phonophobia than the human being would have experienced two hours after receiving the same amount of the meloxicam without the rizatriptan.

25. A method of treating migraine, comprising administering a meloxicam and about 8 mg to about 13 mg of a rizatriptan, based upon the weight of the free base form of rizatriptan, to a human being who is suffering from an acute attack of migraine pain or migraine aura, wherein the meloxicam and the rizatriptan are administered within about 30 minutes of one another, wherein administering the meloxicam to the human being results in a T max of meloxicam of 110 minutes or less, and an AUC 0-24 of meloxicam of about 30 μg·hr/mL to about 50 μg·hr/mL, and wherein two hours after the meloxicam and the rizatriptan are administered, the human being experiences greater relief from phonophobia than the human being would have experienced two hours after receiving the same amount of the rizatriptan without the meloxicam.

26. The method of claim 19 , wherein the rizatriptan is administered in a salt form in an amount that is a molar equivalent to about 10 mg of the free base form of rizatriptan.

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

28. The method of claim 19 , wherein about 15 mg to about 25 mg of the meloxicam is administered to the human being.

29. The method of claim 19 , wherein about 20 mg of the meloxicam is administered to the human being.

30. The method of claim 19 , wherein the human being has a history of inadequate response to prior migraine treatments.

31. The method of claim 30 , wherein the rizatriptan is administered in a salt form in an amount that is a molar equivalent to about 10 mg of the free base form of rizatriptan.

32. The method of claim 30 , wherein about 15 mg to about 25 mg of the meloxicam is administered to the human being.

33. The method of claim 31 , wherein about 20 mg of the meloxicam is administered to the human being.

34. The method of claim 19 , wherein the meloxicam and the rizatriptan are administered simultaneously, and wherein two hours after the meloxicam and the rizatriptan are administered, the human being experiences greater relief from nausea than the human being would have experienced two hours after receiving the same amount of the meloxicam without the rizatriptan.

35. The method of claim 34 , wherein the rizatriptan is administered in a salt form in an amount that is a molar equivalent to about 10 mg of the free base form of rizatriptan.

36. The method of claim 34 , wherein about 15 mg to about 25 mg of the meloxicam is administered to the human being.

37. The method of claim 35 , wherein about 20 mg of the meloxicam is administered to the human being.

38. The method of claim 19 , wherein the meloxicam and the rizatriptan are administered simultaneously, and wherein two hours after the meloxicam and the rizatriptan are administered, the human being experiences greater relief from nausea than the human being would have experienced two hours after receiving the same amount of the rizatriptan without the meloxicam.

39. The method of claim 38 , wherein the rizatriptan is administered in a salt form in an amount that is a molar equivalent to about 10 mg of the free base form of rizatriptan.

40. The method of claim 38 , wherein about 15 mg to about 25 mg of the meloxicam is administered to the human being.

41. The method of claim 39 , wherein about 20 mg of the meloxicam is administered to the human being.

42. The method of claim 20 , wherein the meloxicam and the rizatriptan are administered simultaneously, and wherein two hours after the meloxicam and the rizatriptan are administered, the human being experiences greater relief from vomiting than the human being would have experienced two hours after receiving the same amount of the meloxicam without the rizatriptan.

43. The method of claim 21 , wherein the meloxicam and the rizatriptan are administered simultaneously, and wherein two hours after the meloxicam and the rizatriptan are administered, the human being experiences greater relief from vomiting than the human being would have experienced two hours after receiving the same amount of the rizatriptan without the meloxicam.

44. The method of claim 22 , wherein the meloxicam and the rizatriptan are administered simultaneously, and wherein two hours after the meloxicam and the rizatriptan are administered, the human being experiences greater relief from photophobia than the human being would have experienced two hours after receiving the same amount of the meloxicam without the rizatriptan.

45. The method of claim 23 , wherein the meloxicam and the rizatriptan are administered simultaneously, and wherein two hours after the meloxicam and the rizatriptan are administered, the human being experiences greater relief from photophobia than the human being would have experienced two hours after receiving the same amount of the rizatriptan without the meloxicam.

46. The method of claim 24 , wherein the meloxicam and the rizatriptan are administered simultaneously, and wherein two hours after the meloxicam and the rizatriptan are administered, the human being experiences greater relief from phonophobia than the human being would have experienced two hours after receiving the same amount of the meloxicam without the rizatriptan.

47. The method of claim 25 , wherein the meloxicam and the rizatriptan are administered simultaneously, and wherein two hours after the meloxicam and the rizatriptan are administered, the human being experiences greater relief from phonophobia than the human being would have experienced two hours after receiving the same amount of the rizatriptan without the 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 Oct 3, 2019
From: TABUTEAU, HERRIOT
To: AXSOME THERAPEUTICS, INC.
Reel/Frame 050618/0971 →