US2017145114A1PendingUtilityA1

Biological products

63
Assignee: UCB BIOPHARMA SPRLPriority: May 2, 2002Filed: Jan 27, 2017Published: May 25, 2017
Est. expiryMay 2, 2022(expired)· nominal 20-yr term from priority
C07K 2317/56C07K 16/3061C07K 2317/52A61K 2039/505C07K 2317/40C07K 2317/565C07K 2317/24C07K 16/2851C07K 2317/20C07K 2317/76C07K 16/28C07K 16/2803C07K 2317/92A61K 2039/507C07K 2317/41C07K 16/464A61P 43/00A61K 39/39533C12N 15/11C07K 2317/567C12Q 1/686A61P 35/00G01N 33/53G01N 33/567
63
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Claims

Abstract

There is disclosed antibody molecules containing at least one CDR derived from a mouse monoclonal antibody having specificity for human CD22. There is also disclosed a CDR grafted antibody wherein at least one of the CDRs is a modified CDR. Further disclosed are DNA sequences encoding the chains of the antibody molecules, vectors, transformed host cells and uses of the antibody molecules in the treatment of diseases mediated by cells expressing CD22.

Claims

exact text as granted — not AI-modified
1 - 18 . (canceled) 
     
     
         19 . An antibody molecule having specificity for human CD22 comprising a heavy chain and a light chain wherein the variable domains comprise the amino acid sequences of SEQ ID NO:1 for CDR-H1; SEQ ID NO:3 for CDR-H3; SEQ ID NO:4 for CDR-L1; SEQ ID NO:5 for CDR-L2; and SEQ ID NO:6 for CDR-L3. 
     
     
         20 . The antibody molecule of  claim 19 , which is a CDR-grafted antibody molecule. 
     
     
         21 . The antibody molecule of  claim 19 , wherein the variable domain comprises human acceptor framework regions and non-human donor CDRs. 
     
     
         22 . A composition comprising the antibody molecule of any one of  claims 19 - 21 . 
     
     
         23 . The composition according to  claim 22 , comprising a pharmaceutically acceptable excipient, diluent, or carrier. 
     
     
         24 . The composition according to  claim 22 , additionally comprising anti-T cell, anti-IFNγ, anti-LPS antibodies, or a non-antibody ingredient.

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