IP Library Granted Patent US 7,122,566
Granted Patent B1
US 7,122,566 · App. 11/364,468 · Granted Oct 17, 2006

Metaxalone products, method of manufacture, and method of use

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Quick Facts
Patent No.
US 7,122,566
App. No.
11/364,468
Granted
Oct 17, 2006
Kind
B1
Abstract

Disclosed herein is a method of using metaxalone. In one embodiment, the method comprises obtaining metaxalone from a container providing information that metaxalone affects the activity of a cytochrome p450 isozyme. In another embodiment, the method comprises informing a user that metaxalone affects the activity of a cytochrome p450 isozyme. Also included are articles of manufacture comprising a container containing a dosage form of metaxalone, wherein the container is associated with published material informing that metaxalone affects activity of a cytochrome p450 isozyme. Also disclosed are a method of treatment and a method of manufacturing a metaxalone product.

Claims (28)

1. A method of using metaxalone for treating a patient's condition, comprising

providing a patient with metaxalone; and

informing the patient or a medical care worker that metaxalone affects activity of a cytochrome p450 isozyme, and that administration of metaxalone with a substance that affects activity of a cytochrome p450 isozyme can affect plasma concentration, safety, efficacy or any combination thereof of metaxalone, the substance, or both.

2. The method of claim 1 , wherein the substance is an active agent with a narrow therapeutic index.

3. The method of claim 2 , wherein the substance is a substrate of CYP1A2, CYP3A4, CYP2B6, CYP2C19, CYP2D6, CYP2E1, or CYP2C9.

4. The method of claim 2 , wherein the substance is warfarin, phenytoin, fosphenytoin, thioridazine, or theophylline.

5. A method of using metaxalone to treat a patient's condition, comprising:

providing a patient with metaxalone; and

informing the patient or a medical care worker that a cytochrome p450 isozyme metabolizing metaxalone is CYP1A2 or CYP2C19 and that administration of metaxalone and a substance that is a substrate, inhibitor, or inducer of CYP1A2 or CYP2C19 can affect plasma concentration, safety, efficacy or any combination thereof of metaxalone, the substance, or both.

6. A method of using metaxalone to treat a patient's condition, comprising:

providing a patient with metaxalone; and

informing the patient or a medical care worker that metaxalone is an inhibitor, inducer, or substrate of a cytochrome p450 isozyme and administration of metaxalone with a substance that is an inhibitor, inducer, or substrate of the cytochrome p450 isozyme can affect the plasma concentration, safety or efficacy of the substance.

7. The method of claim 6 , wherein the cytochrome p450 isozyme is CYP1A2, CYP3A4, CYP2B6, CYP2C19, CYP2D6, CYP2E1, or CYP2C9.

8. The method of claim 6 , wherein the substance is an active agent with a narrow therapeutic index.

9. The method of claim 8 , wherein the substance is a substrate of CYP1A2, CYP3A4, CYP2B6, CYP2C19, CYP2D6, CYP2E1, or CYP2C9.

10. The method of claim 8 , wherein the active agent with the narrow therapeutic index is an inhibitor of the cytochrome p450 isozyme.

11. The method of claim 8 , wherein the active agent with the narrow therapeutic index is an inducer of the cytochrome p450 isozyme.

12. The method of claim 8 , wherein the active agent with the narrow therapeutic index is a substrate of the cytochrome p450 isozyme.

13. The method of claim 8 , wherein the substance is warfarin, phenytoin, fosphenytoin, thioridazine, or theophylline.

14. The method of claim 1 , wherein metaxalone is an inducer of the cytochrome p450 isozyme.

15. The method of claim 14 , wherein the cytochrome p450 isozyme is CYP1A2 or CYP3A4.

16. The method of claim 1 , wherein metaxalone is an inhibitor of the cytochrome p450 isozyme.

17. The method of claim 16 , wherein the cytochrome p450 isozyme is CYP1A2, CYP2B6, CYP2C19, CYP2D6, CYP2C9, CYP2E1, or CYP3A4.

18. The method of claim 1 , wherein metaxalone is a substrate of the cytochrome p450 isozyme.

19. The method of claim 18 , wherein the cytochrome p450 isozyme is CYP1A2 or CYP2C19.

20. The method of claim 1 , wherein the patient is a human patient.

21. The method of claim 1 , wherein the patient is a patient with a musculoskeletal condition.

22. The method of claim 1 , wherein the patient is a patient receiving metaxalone therapy.

Assignments (7)
MERGER Recorded Nov 30, 2012
From: PHARMACEUTICAL IP HOLDING, INC.
To: MPC OLDCO, INC.
Reel/Frame 029381/0117 →
MERGER Recorded Nov 30, 2012
From: MPC OLDCO, INC.
To: MPC MERGER SUB, INC.
Reel/Frame 029381/0439 →
MERGER Recorded Nov 30, 2012
From: MPC MERGER SUB, INC.
To: TAKEDA PHARMACEUTICALS U.S.A., INC.
Reel/Frame 029381/0477 →
RELEASE OF SECURITY INTEREST Recorded Aug 12, 2011
From: UBS AG, STAMFORD BRANCH, A SWISS BANKING INSTITUTION
To: MUTUAL PHARMACEUTICAL COMPANY, INC., A PENNSYLVANIA CORPORATION
Reel/Frame 026744/0541 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 26, 2009
From: MUTUAL PHARMACEUTICAL COMPANY, INC.
To: PHARMACEUTICAL IP HOLDING, INC.
Reel/Frame 022315/0313 →
PATENT SECURITY AGREEMENT Recorded Jan 30, 2007
From: MUTUAL PHARMACEUTICAL COMPANY, INC.
To: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
Reel/Frame 018826/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 28, 2006
From: DU, JIE; ROBERTS, RICHARD H.
To: MUTUAL PHARMACEUTICAL COMPANY, INC.
Reel/Frame 017638/0370 →