US2015291688A1PendingUtilityA1

Methods For Treating Tweak-Related Conditions

Assignee: BIOGEN IDEC INCPriority: Apr 9, 2002Filed: Mar 18, 2015Published: Oct 15, 2015
Est. expiryApr 9, 2022(expired)· nominal 20-yr term from priority
A61P 43/00A61P 9/00A61P 9/04A61P 3/04A61P 25/00A61P 29/00C07K 2319/00A61P 13/00A61K 45/06C07K 14/70575A61P 17/00C07K 16/241A61P 1/16A61P 1/04A61K 39/39533A61P 21/00A61K 39/3955A61P 19/00A61P 11/00C07K 2319/30A61K 39/39566C07K 16/22A61P 19/04A01K 2217/05A61K 2039/505A61P 13/04A61K 38/191A61K 38/00C07K 14/525A61P 1/18A61P 13/02C07K 16/2875A61P 15/00A61P 13/12A61P 15/08A61P 1/00
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Claims

Abstract

The present invention provides methods and agents for the treatment of TWEAK-related conditions, including cardiac, liver, kidney, lung, adipose, skeletal, muscle, neuronal, bone and cartilage conditions. The invention also provides methods for identifying TWEAK agonists or antagonists for the treatment of TWEAK-related conditions. Additionally, the invention provides transgenic animals that express an exogenous DNA encoding a TWEAK polypeptide, or fragments, analogs, or muteins thereof, and methods for using such animals to identify TWEAK agonists or antagonists. The invention further provides methods for diagnosing a disease based on TWEAK expression. The invention also provides methods for affecting cellular differentiation of progenitor cells using TWEAK polypeptides, agonists, or antagonists.

Claims

exact text as granted — not AI-modified
1 .- 12 . (canceled) 
     
     
         13 . A method for treating muscle atrophy in a human subject in need thereof, the method comprising administering to the human subject a therapeutically effective amount of a TWEAK antagonist, wherein the TWEAK antagonist is an antibody, or an antigen-binding fragment thereof, that binds human TWEAK. 
     
     
         14 . The method of  claim 13 , wherein the muscle atrophy is muscular dystrophy. 
     
     
         15 . The method of  claim 13 , wherein the muscle atrophy is a mitochondrial myopathy, a lipid myopathy, a central tubular myopathy, rhabdomyolysis, or an alcoholic myopathy. 
     
     
         16 . The method of  claim 13 , wherein the muscle atrophy is the result of a neuronal disease. 
     
     
         17 . The method of claim  41 , wherein the neuronal disease is amyotrophic lateral sclerosis (ALS). 
     
     
         18 . The method of  claim 13 , wherein the muscle atrophy is cachexia. 
     
     
         19 . The method of  claim 13 , wherein the muscle atrophy is the result of polymyositis, an inflammatory myopathy, or a glucocorticoid induced atrophy. 
     
     
         20 . The method of  claim 13 , wherein the human subject has cancer. 
     
     
         21 . The method of  claim 13 , wherein the anti-human TWEAK antibody or the antigen-binding fragment thereof is human, humanized, or chimeric. 
     
     
         22 . The method of  claim 13 , wherein the TWEAK antagonist is used in combination with progenitor cell therapy. 
     
     
         23 . The method of  claim 13 , wherein the TWEAK antagonist is used in combination with tissue transplantation therapy.

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