US2018111983A1PendingUtilityA1
Treatment of Fibrodysplasia Ossificans Progressiva
Est. expirySep 12, 2034(~8.1 yrs left)· nominal 20-yr term from priority
A61P 43/00A61P 19/00A61P 21/00A61P 19/04A61P 19/08A61K 38/179C07K 16/2863C07K 2319/30A61K 39/39533C07K 16/18C07K 2317/33A61K 2039/505C07K 14/705C07K 16/22C07K 2317/21C07K 2317/24C07K 16/28A61K 39/3955A61K 2300/00A61K 31/138
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Claims
Abstract
Methods for treating Fibrodysplasia Ossificans Progressiva (FOP) are provided. Such methods involve administering to a subject having FOP an effective regime of an activin receptor type 2A (ACVR2A) and/or an activin receptor type 2B (ACVR2B) antagonist or an activin receptor type 1 (ACVR1) antagonist. Antagonists include fusion proteins of one or more extracellular domains (ECDs) of ACVR2A, ACVR2B and/or ACVR1 and the Fc domain of an immunoglobulin heavy chain, and antibodies against ACVR2A, ACVR2B, ACVR1 or Activin A.
Claims
exact text as granted — not AI-modified1 . A method of treating Fibrodysplasia Ossificans Progressiva (FOP), comprising administering to a subject having FOP an effective regime of an activin receptor type 2A (ACVR2A) and/or an activin receptor type 2B (ACVR2B) antagonist.
2 - 13 . (canceled)
14 . A method of treating Fibrodysplasia Ossificans Progressiva (FOP), comprising administering to a subject having FOP an effective regime of an activin receptor type 1 (ACVR1) antagonist.
15 - 18 . (canceled)
19 . A method of treating Fibrodysplasia Ossificans Progressiva (FOP), comprising administering to a subject having FOP an effective regime of an activin receptor type 2A (ACVR2A) and/or an activin receptor type 2B (ACVR2B) antagonist in combination with an activin receptor type 1 (ACVR1) antagonist.
20 - 23 . (canceled)
24 . A method of treating Fibrodysplasia Ossificans Progressiva (FOP), comprising administering to a subject having FOP an effective regime of an antibody against Activin A.
25 . The method of claim 24 , wherein the antibody competes for binding with antibody comprising the heavy and light chain variable regions of the antibody designated H4H10446P, H4H10430P or A1.
26 . The method of claim 24 , wherein the antibody comprises the heavy and light chain variable regions of the antibody designated H4H10446P, H4H10430P or A1.
27 . The method of claim 24 , wherein the antibody is chimeric, veneered, humanized or human antibody.
28 . The method of claim 24 wherein the antibody is an intact antibody.
29 . The method of claim 24 , wherein the antibody is a human kappa IgG1 antibody.
30 . The method of claim 25 , wherein the antibody is a human kappa IgG1 antibody.
31 . The method of claim 26 , wherein the antibody is a human kappa IgG1 antibody.
32 . The method of claim 27 , wherein the antibody is a human kappa IgG1 antibody.
33 . The method of claim 28 , wherein the antibody is a human kappa IgG1 antibody.Join the waitlist — get patent alerts
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