Compositions for the treatment of sarcopenia or disuse atrophy

US2021275639A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2021275639-A1
Application numberUS-201917261314-A
CountryUS
Kind codeA1
Filing dateJul 19, 2019
Priority dateJul 20, 2018
Publication dateSep 9, 2021
Grant date

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

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The present invention relates to a substance that activates the GDF5 pathway, for use in a method for the treatment of age-related sarcopenia or disuse atrophy.

First claim

Opening claim text (preview).

1 . A GDF5 pathway-activating substance for use in a method for the treatment or prevention of sarcopenia or disuse atrophy. 2 . A GDF5 pathway-activating substance for use in treating or preventing muscle weakness in a myopathy or neuromuscular disease, alone or in combination with a treatment of said myopathy or neuromuscular disease. 3 . The substance for use according to claim 1 , wherein the substance is selected from compounds that increase the activity of GDF5 or compounds that increase the expression of GDF5. 4 . The substance for use according to claim 1 , wherein the substance is recombinant human GDF5. 5 . The substance for use according to claim 1 , wherein the substance is recombinant human CaVβ1-E or a vector encoding human CaVβ1-E. 6 . The substance for use according to claim 1 , wherein the substance is administered to a subject aged 50 years or older, in particular 55 years or older, in particular 60 years or older, more particularly 65 years or older, even more particularly 70 years or older, such as 75 years or older or even 80 years or older. 7 . The substance for use according to claim 1 , wherein the substance is administered via the oral, nasal, intravascular, intramuscular, intraperitoneal route, transdermal or subcutaneous route. 8 . The substance for use according to claim 1 , wherein the substance is administered on a regular basis, such as on a monthly basis, in particular on a weekly basis, or more particularly on a daily basis. 9 . The substance for use according to claim 1 , wherein the treatment of sarcopenia results in an increase of muscle mass and/or function, an increase in physical performance or mobility, and/or an increase in muscle strength. 10 . A pharmaceutical composition comprising a GDF5 pathway-activating substance and a pharmaceutically acceptable carrier. 11 . The pharmaceutical composition according to claim 10 , wherein the substance is recombinant human GDF5. 12 . A GDF5 pathway-activating substance, for use as a medicament. 13 . The substance for use according to claim 12 , wherein said substance is recombinant human GDF5. 14 . A method for the diagnosis of sarcopenia in a subject, comprising determining the level of GDF5 in a biological sample of said subject.

Assignees

Inventors

Classifications

  • Anabolic agents (androgens A61P5/26) · CPC title

  • Drugs for disorders of the muscular or neuromuscular system · CPC title

  • Muscular dystrophy · CPC title

  • Assays involving growth factors · CPC title

  • involving hormones {or other non-cytokine intercellular protein regulatory factors such as growth factors, including receptors to hormones and growth factors} · CPC title

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Frequently asked questions

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What does patent US2021275639A1 cover?
The present invention relates to a substance that activates the GDF5 pathway, for use in a method for the treatment of age-related sarcopenia or disuse atrophy.
Who is the assignee on this patent?
Association Inst De Myologie, Inst Nat Sante Rech Med, Univ Sorbonne
What technology area does this patent fall under?
Primary CPC classification A61K38/1841. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Thu Sep 09 2021 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).