US2018030148A1PendingUtilityA1

Compositions and methods for the detection diagnosis and therapy of hematological malignancies

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Assignee: CORIXA CORPPriority: Jan 22, 2002Filed: Sep 26, 2017Published: Feb 1, 2018
Est. expiryJan 22, 2022(expired)· nominal 20-yr term from priority
C12Q 2600/112C07K 14/70535C12N 5/06A61K 2039/505C12Q 2600/118C07K 2317/92C07K 16/18C12Q 1/6886A61K 47/6851C07K 14/47C07K 16/3061C12N 15/63C07K 16/28C07K 2317/24C07K 2317/56C12N 15/11A61K 38/00C12Q 2600/106C07K 2317/55C12Q 2600/158C07K 2317/569A61K 51/1018A61P 35/00G01N 33/57505G01N 33/57426A61K 39/0011A61K 39/00A61K 40/416A61K 40/42A61K 40/22A61K 40/11A61K 2239/48
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Claims

Abstract

Disclosed are methods and compositions for the detection, diagnosis, prognosis, and therapy of hematological malignancies, and in particular, B cell leukemias, lymphomas and multiple myelomas. Disclosed are compositions, methods and kits for eliciting immune and T cell responses to specific malignancy-related antigenic polypeptides and antigenic polypeptide fragments thereof in an animal. Also disclosed are compositions and methods for use in the identification of cells and biological samples containing one or more hematological malignancy-related compositions, and methods for the detection and diagnosis of such diseases and affected cell types. Also disclosed are diagnostic and therapeutic kits, as well as methods for the diagnosis, therapy and/or prevention of a variety of leukemias and lymphomas.

Claims

exact text as granted — not AI-modified
1 - 16 . (canceled) 
     
     
         17 . A method for treating non-Hodgkin's lymphoma (NHL) in a mammalian subject wherein a B-cell from said subject overexpresses SEQ ID NO:4, comprising administering to said subject an effective amount of an isolated monoclonal antibody that specifically binds to a polypeptide comprising the sequence set forth in SEQ ID NO: 4, wherein said monoclonal antibody has a binding constant for SEQ ID NO:4 that exceeds 10 3  L/mol. 
     
     
         18 . The method of  claim 17 , wherein said antibody is a humanized antibody. 
     
     
         19 . The method of claim  7 , wherein said antibody is a chimeric antibody. 
     
     
         20 . The method of  claim 17 , wherein said antibody is a Fab fragment. 
     
     
         21 . The method of  claim 17 , wherein said antibody is a Fv fragment. 
     
     
         22 . The method of  claim 17 , wherein said antibody is a scFv. 
     
     
         23 . The method of  claim 17 , wherein said antibody further comprises a therapeutic moiety. 
     
     
         24 . The method of  claim 23 , wherein the therapeutic moiety is a radionuclide. 
     
     
         25 . The method of  claim 24 , wherein the radionuclide is chosen from:  90 Y,  123 I,  125 I,  131 I,  186 Re,  211 At, and  212 Bi. 
     
     
         26 . The method of  claim 17 , wherein the mammalian subject is a human. 
     
     
         27 . The method of  claim 17 , wherein administration is intravenous.

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