US2005013814A1PendingUtilityA1

Methods for treating rheumatoid arthritis using IL-17 antagonists

Assignee: IMMUNEX CORPPriority: Oct 18, 2000Filed: Aug 13, 2004Published: Jan 20, 2005
Est. expiryOct 18, 2020(expired)· nominal 20-yr term from priority
A61P 29/00A61P 19/02C07K 2319/30A61K 38/1793A61K 31/519A61K 2039/505C07K 2319/00A61K 38/20
58
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Claims

Abstract

A method of treating a mammal afflicted with rheumatoid arthritis comprising administering a soluble form of IL-17 receptor is disclosed.

Claims

exact text as granted — not AI-modified
1 . A method of treating an individual afflicted with rheumatoid arthritis comprising administering to the individual IL-17 receptor.  
     
     
         2 . A method of treating an individual afflicted with rheumatoid arthritis comprising administering to the individual a therapeutic comprising a polypeptide selected from the group consisting of the extracellular domain of human IL-17 receptor and a fragment of the extracellular domain of human IL-17 receptor, wherein the fragment inhibits the binding of IL-17 receptor and IL-17.  
     
     
         3 . A method of treating an individual afflicted with rheumatoid arthritis, the method comprising administering to the individual a therapeutic comprising a polypeptide selected from the group consisting of: 
 (a) a polypeptide having amino acids 33 through 322 of SEQ ID NO:1;    (b) a polypeptide that is at least about 70% identical to the polypeptide of (a) and that binds IL-17; and    (c) fragments of the proteins of (a) or (b), that bind IL-17.    
     
     
         4 . The method of  claim 2 , wherein the therapeutic is a chimeric fusion protein that further comprises an immunoglobulin Fc.  
     
     
         5 . The method according to  claim 2 , further comprising administering, one or more therapeutics selected from the group consisting of a TNF antagonist and an IL-1 antagonist.  
     
     
         6 . The method of  claim 5 , wherein the IL-1 antagonist is selected from the group consisting of soluble IL-1 receptor type II, IL-IR type I antibody, IL-1 receptor antagonist, and fusion protein comprising soluble IL-1 receptor type I, and soluble IL-1 receptor accessory protein.  
     
     
         7 . The method of  claim 5  wherein the TNF antagonist is selected from the group consisting of TNF antibodies, soluble TNF receptor p75, and soluble TNF receptor p55.

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