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Last Updated: December 16, 2025

Claims for Patent: 10,292,954


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Summary for Patent: 10,292,954
Title:Composition and method for muscle repair and regeneration
Abstract:The invention provides methods for muscle repair or regeneration comprising administering therapeutically effective amounts of RAR agonists or stem cells that are pretreated with contact with a RAR agonist to a subject at a site of muscle damage. Additionally, the invention provides compositions comprising RAR agonist treated stem cells and methods of use of said cells for muscle repair or regeneration. In one embodiment, the stem cells are mesenchymal stem cells. In one embodiment, the RAR agonist is an RARγ agonist. In one embodiment, administration of the RAR agonist is begun during a period of increased endogenous retinoid signaling in the subject resulting from incurrence of the damaged muscle tissue.
Inventor(s):Masahiro Iwamoto, Maurizio Pacifici
Assignee: Thomas Jefferson University
Application Number:US15/674,357
Patent Claims: 1. A method of treating a subject suffering from a muscle damaging myopathy, comprising administering to the subject a therapeutically effective amount of a retinoic acid receptor gamma (RARγ) agonist, wherein the RARγ agonist is 4-[(E)-2-[5,6,7,8-Tetrahydro-5,5,8,8-tetramethyl-3-(1H-pyrazol-1-ylmethyl)-2-naphthalenyl]-ethenyl]benzoic acid or a pharmaceutically acceptable salt thereof.

2. The method of claim 1, wherein the muscle damaging myopathy is myositis ossificans.

3. The method of claim 1, wherein the muscle damaging myopathy is a congenital myopathy.

4. The method of claim 1, wherein the muscle damaging myopathy is an acquired myopathy.

5. The method of claim 1, wherein said RARγ agonist is administered locally.

6. The method of claim 1, wherein said RARγ agonist is administered systemically.

7. A method of inducing progenitor stem cells to undergo myogenic differentiation in a subject suffering from a muscle damaging myopathy, comprising administering to the subject a therapeutically effective amount of an RARγ agonist, wherein the RARγ agonist is 4-[(E)-2-[5,6,7,8-Tetrahydro-5,5,8,8-tetramethyl-3-(1H-pyrazol-1-ylmethyl)-2-naphthalenyl]-ethenyl]benzoic acid or a pharmaceutically acceptable salt thereof.

8. The method of claim 7, wherein the muscle damaging myopathy is myositis ossificans.

9. The method of claim 7, wherein the muscle damaging myopathy is a congenital myopathy.

10. The method of claim 7, wherein the muscle damaging myopathy is an acquired myopathy.

11. The method of claim 7, wherein said RARγ agonist is administered locally.

12. The method of claim 7, wherein said RARγ agonist is administered systemically.

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