US2015313881A1PendingUtilityA1

Therapeutic Methods for Type I Diabetes

Assignee: UNIV MASSACHUSETTSPriority: Mar 29, 2005Filed: Apr 29, 2015Published: Nov 5, 2015
Est. expiryMar 29, 2025(expired)· nominal 20-yr term from priority
A61K 31/4725A61K 31/4535A61K 31/55A61K 31/18A61K 31/415A61P 3/10A61K 31/506A61K 31/40A61K 31/425A61K 31/416A61K 31/381A61K 31/4025A61K 31/5377A61K 31/437A61K 31/497A61K 31/54A61K 31/70A61K 31/50A61K 31/428A61K 31/42A61K 31/445
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Claims

Abstract

The invention relates to the treatment and prevention of type I diabetes. More specifically, the invention relates to compounds that treat or prevent the body's immune system from destroying β-cells (i.e., insulin-producing cells in the pancreatic islets of Langerhans) by inhibition of JNK2, selective inhibition of JNK2, or inhibition of the expression of the MAPK9 gene or gene product. In one embodiment, the present invention contemplates the diagnosis, identification, production, and use of compounds which modulate MAPK9 gene expression or the activity of the MAPK9 gene product including but not limited to, JNK2, the nucleic acid encoding MAPK9 and homologues, analogues, and deletions thereof, as well as antisense, ribozyme, triple helix, antibody, and polypeptide molecules as well as small inorganic molecules. The present invention contemplates a variety of pharmaceutical formulations and routes of administration for such compounds.

Claims

exact text as granted — not AI-modified
1 - 20 . (canceled) 
     
     
         21 . A method for treating type I diabetes in a subject, comprising administering a compound comprising 5-aminoanthra(9,1-cd)isothiazol-6-one. 
     
     
         22 . The method of  claim 21 , wherein said compound inhibits enzymatic activity of a JNK2 protein in said subject. 
     
     
         23 . The method of  claim 21 , wherein said compound has minimally inhibits enzymatic activity of a JNK1 protein in said subject. 
     
     
         24 . The method of  claim 23 , wherein said JNK1 enzymatic activity is not inhibited. 
     
     
         25 . The method of  claim 21 , wherein said compound does not result in an adverse drug reaction to said subject.

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