US2010316599A1PendingUtilityA1

Methods of treating cancer using il-21

Assignee: ZYMOGENETICS INCPriority: Jun 7, 2002Filed: Apr 28, 2010Published: Dec 16, 2010
Est. expiryJun 7, 2022(expired)· nominal 20-yr term from priority
A61P 35/04A61P 37/02A61P 37/04A61P 9/00A61P 31/14A61P 33/02A61P 35/02A61P 35/00A61P 31/18A61P 31/06A61P 31/22A61P 31/20A61P 25/00A61P 31/04A61P 31/10A61P 31/16A61P 31/00A61P 31/12A61P 19/02A61P 1/04A61P 1/16A61P 1/00A61P 11/00A61K 38/193C07K 2317/73C07K 14/54A61K 38/2086A61K 38/20C07K 16/2878A61K 38/2026A61K 45/06A61K 38/2013Y02A50/30
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Claims

Abstract

Methods for treating mammals with cancer using molecules that have an IL-21 functional activity are described. The molecules having IL-21 functional activities include polypeptides that have homology to the human IL-21 polypeptide sequence and proteins fused to a polypeptide with IL-21 functional activity. The molecules can be used as a monotherapy or in combination with other known cancer therapeutics.

Claims

exact text as granted — not AI-modified
1 . A method of treating Non-Hodgkins lymphoma comprising administering to a subject having Non-Hodgkins lymphoma in need thereof a therapeutically effective amount of an IL-21 polypeptide comprising residues 32 (Gln) to 162 (Ser) of SEQ ID NO:2. 
     
     
         2 . The method according to  claim 1 , wherein the polypeptide has been shown to not cause proliferation of isolated cancer cells prior to administration to the subject. 
     
     
         3 . The method of  claim 1 , wherein there is a tumor response. 
     
     
         4 . The method of  claim 3 , wherein a tumor response is measured as complete response or partial response. 
     
     
         5 . A method of treating Non-Hodgkins lymphoma comprising administering to a subject having Non-Hodgkins lymphoma in need thereof a therapeutically effective amount of a fusion protein comprising a first IL-21 polypeptide comprising residues 32 to 162 of SEQ ID NO:2 and a second polypeptide. 
     
     
         6 . The method according to  claim 5 , wherein the polypeptide has been shown not to cause proliferation of isolated cancer cells prior to administration to the subject. 
     
     
         7 . The method of  claim 5 , wherein there is a tumor response. 
     
     
         8 . The method of  claim 7 , wherein a tumor response is measured as complete response or partial response. 
     
     
         9 . A method of tumor vaccination comprising administering to a subject in need thereof an IL-21 polypeptide comprising residues 32 to 162 of SEQ ID NO:2 in combination with a tumor antigen protein or tumor antigen peptide, wherein said antigen is a tumor associated antigen (TAA) from Non-Hodgkins lymphoma.

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