IP Library Granted Patent US 7,714,006
Granted Patent B1
US 7,714,006 · App. 11/182,661 · Granted May 11, 2010

Methods of modifying the bioavailability of metaxalone

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Quick Facts
Patent No.
US 7,714,006
App. No.
11/182,661
Granted
May 11, 2010
Kind
B1
Abstract

A method of increasing the bioavailability, and decreasing the effect of age on the bioavailability, of metaxalone, by administration of an oral dosage form with food is provided, as well as an article of manufacture comprising an oral dosage form of metaxalone in a suitable container and associated with printed labeling which describes the increased bioavailability, and decreased effect of age on bioavailability, of the medication in the container, when taken with food.

Claims (36)

1. A method of reducing the effect of a patient's age on the oral bioavailability of metaxalone in a patient receiving metaxalone therapy comprising administering to the patient a therapeutically effective amount of metaxalone in a pharmaceutical composition with food over the course of said therapy.

2. The method of claim 1 , wherein the therapeutically effective amount is 200 mg to 900 mg.

3. The method of claim 1 , wherein the therapeutically effective amount is 400 mg to 800 mg.

4. The method of claim 1 , wherein the administration to the patient occurs between 30 minutes prior to 2 hours after consuming food.

5. The method of claim 1 , wherein the administration to the patient is substantially at the same time as the consumption of food.

6. The method of claim 4 , wherein the administration to the patient is within 15 minutes of the consumption of food.

7. The method of claim 1 , wherein the pharmaceutical composition comprises a tablet.

8. The method of claim 1 , wherein the tablet is in unit dosage form.

9. The method of claim 1 , further comprising informing the patient that the administration of a therapeutically effective amount of metaxalone in a pharmaceutical composition with food results in a decreased effect of patient's age on bioavailability of metaxalone, compared to administration without food.

10. The method of claim 1 , wherein the metaxalone is from a container with printed labeling advising that administration of a therapeutically effective amount of metaxalone in a pharmaceutical composition with food results in a decreased effect of patient's age on bioavailability of metaxalone, compared to administration without food.

11. A method of using metaxalone in the treatment of musculoskeletal conditions comprising:

administering to a patient with a therapeutically effective amount of metaxalone; and

informing the patient that the administration of metaxalone with food results in a decrease in the effect of patient's age on at least one of C(max), AUC(last), and AUC(inf) of metaxalone compared to administration without food.

12. The method according to claim 11 , wherein the therapeutically effective amount of metaxalone comprises 200 mg to 900 mg of metaxalone.

13. The method according to claim 12 , wherein the therapeutically effective amount of metaxalone comprises 400 mg to 800 mg of metaxalone.

14. The method according to claim 11 , wherein the metaxalone is provided in tablet form.

15. The method according to claim 14 , wherein the tablet is in unit dosage form.

16. A method of using metaxalone in the treatment of musculoskeletal conditions comprising:

informing a patient with musculoskeletal conditions that the administration of a therapeutically effective amount of metaxalone with food results in a decrease in the effect of patient's age on at least one of C(max), AUC(last), and AUC(inf) of metaxalone compared to administration without food,

wherein the patient administers the metaxalone in accordance with the information provided.

17. A method of using metaxalone in the treatment of musculoskeletal conditions comprising:

obtaining the metaxalone from a container providing information that the administration of metaxalone with food decreases the effect of patient's age on at least one of C(max), AUC(last), and AUC(inf) of metaxalone compared to administration without food, and

ingesting the metaxalone with food.

18. A method of using metaxalone in the treatment of musculoskeletal conditions comprising:

administering to a patient in need of treatment a therapeutically effective amount of metaxalone, with food; and

informing the patient that the administration of a therapeutically effective amount of metaxalone in a pharmaceutical composition with food results in a decrease in the effect of patient's age on at least one of C(max), AUC(last), and AUC(inf) of metaxalone, as compared to administration of metaxalone in a fasted state;

wherein the administration of metaxalone with food results in a decrease in the effect of patient's age on at least one of C(max), AUC(last), and AUC(inf) of metaxalone, as compared to administration of metaxalone in a fasted state.

19. The method according to claim 18 , wherein the metaxalone is from a container with printed labeling advising that administration with food results in a decrease in the effect of patient's age on at least one of C(max), AUC(last), and AUC(inf) of metaxalone, as compared to administration of metaxalone in a fasted state.

20. The method according to claim 18 , wherein the metaxalone is provided in tablet form.

21. The method according to claim 20 , wherein the metaxalone is provided in 400 mg tablet form.

22. The method according to claim 18 , wherein the printed labeling further advises that administration of the metaxalone with food results in an increase in the C(max) of 177.5%.

23. The method according to claim 18 , wherein the printed labeling further advises that administration of the metaxalone with food results in an increase in the AUC(last) of 123.5%.

24. The method according to claim 18 , wherein the printed labeling further advises that administration of the metaxalone with food results in an increase in AUC(inf) of 115.4%.

25. The method according to claim 18 , wherein the metaxalone is provided in 400 mg tablet form, and the printed labeling further advises that administration of metaxalone with food results in an increase in the C(max), AUC(last), and AUC(inf), of 177.5%, 123.5%, and 115.4%, respectively, compared to administration of metaxalone in a fasted state.

26. A method of achieving consistent plasma levels of metaxalone in any given patient regardless of patient's age comprising administering to a patient a therapeutically effective amount of metaxalone with food, wherein said administration achieves consistent levels of metaxalone in any given patient regardless of patient's age.

27. A method of reducing variations in metaxalone bioavailability comprising administering to a patient with food a therapeutically effective amount of metaxalone in a pharmaceutical composition, wherein said administration reduces variations in metaxalone bioavailability.

Assignments (6)
CORRESPONDENTS ADDRESS CORRECTION Recorded Dec 15, 2016
From: KING PHARMACEUTICALS RESEARCH & DEVELOPMENT, INC.
To: KING PHARMACEUTICALS RESEARCH & DEVELOPMENT, INC.
Reel/Frame 040940/0494 →
RELEASE OF SECURITY INTEREST Recorded Feb 3, 2011
From: CREDIT SUISSE AG
To: KING PHARMACEUTICALS RESEARCH AND DEVELOPMENT, INC.
Reel/Frame 025738/0132 →
SECURITY AGREEMENT Recorded May 13, 2010
From: KING PHARMACEUTICALS RESEARCH AND DEVELOPMENT, INC.
To: CREDIT SUISSE AG
Reel/Frame 025703/0628 →
RELEASE OF SECURITY INTEREST Recorded May 11, 2010
From: KING PHARMACEUTICALS RESEARCH AND DEVELOPMENT, INC.
To: CREDIT SUISSE AG
Reel/Frame 024369/0022 →
SECURITY AGREEMENT Recorded Dec 30, 2008
From: KING PHARMACEUTICALS RESEARCH & DEVELOPMENT, INC.
To: CREDIT SUISSE, AS AGENT
Reel/Frame 022034/0870 →
CHANGE OF NAME Recorded Nov 20, 2006
From: JONES PHARMA INCORPORATED
To: KING PHARMACEUTICALS RESEARCH & DEVELOPMENT, INC.
Reel/Frame 018621/0312 →