US2018037665A1PendingUtilityA1

Plasma kallikrein binding proteins

Assignee: DYAX CORPPriority: Jan 6, 2010Filed: Sep 15, 2017Published: Feb 8, 2018
Est. expiryJan 6, 2030(~3.4 yrs left)· nominal 20-yr term from priority
A61P 9/10A61P 7/10A61P 7/00A61P 7/02A61P 9/00A61P 43/00A61P 29/00A61P 25/04A61P 31/04A61P 17/02A61P 1/00A61P 1/02A61P 11/00A61P 13/12A61P 19/06A61P 19/02C07K 2317/92C07K 16/40C07K 2317/76A61K 2039/505A61K 49/0004
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Claims

Abstract

Plasma kallikrein binding proteins and methods of using such proteins are described.

Claims

exact text as granted — not AI-modified
1 . (canceled) 
     
     
         2 . An isolated monoclonal antibody, which binds human plasma kallikrein (pKal), wherein the monoclonal antibody binds human plasma prekallikrein less effectively relative to the human pKal by a factor of at least 10 fold. 
     
     
         3 . The isolated monoclonal antibody of  claim 2 , which binds human plasma prekallikrein less effectively relative to the human pKal by a factor of at least 100 fold. 
     
     
         4 . The isolated monoclonal antibody of  claim 2 , which binds human plasma prekallikrein less effectively relative to the human pKal by a factor of at least 1000 fold. 
     
     
         5 . The isolated monoclonal antibody of  claim 2 , which competes with epi-Kal2 for binding to the human pKal. 
     
     
         6 . The isolated monoclonal antibody of  claim 2 , which competes with AEBSF for binding to the human pKal. 
     
     
         7 . The isolated monoclonal antibody of  claim 2 , which decreases the catalytic activity of the human pKal as compared to the catalytic activity of the human pKal in the absence of the monoclonal antibody and under the same conditions. 
     
     
         8 . The isolated monoclonal antibody of  claim 7 , wherein the monoclonal antibody decreases the production of Factor XIIa or bradykinin by at least 50% as compared to the production of Factor XIIa or bradykinin in the absence of the monoclonal antibody and under the same conditions. 
     
     
         9 . The isolated monoclonal antibody of  claim 8 , wherein the monoclonal antibody decreases the production of Factor XIIa or bradykinin by at least 75% as compared to the production of Factor XIIa or bradykinin in the absence of the monoclonal antibody and under the same conditions. 
     
     
         10 . The isolated monoclonal antibody of  claim 8 , wherein the monoclonal antibody decreases the production of Factor XIIa or bradykinin by at least 90% as compared to the production of Factor XIIa or bradykinin in the absence of the monoclonal antibody and under the same conditions. 
     
     
         11 . The isolated monoclonal antibody of  claim 2 , which binds an epitope comprising one or more amino acids of His434, Asp483, and Ser578 of SEQ ID NO:2. 
     
     
         12 . The isolated monoclonal antibody of  claim 2 , which binds an epitope comprising one or more amino acids of Arg551, Gln553, Tyr555, Thr558, and Arg560 of SEQ ID NO:2. 
     
     
         13 . The isolated monoclonal antibody of  claim 2 , which binds an epitope comprising one or more amino acids of 5478, N481, 5525, and K526 of SEQ ID NO:2. 
     
     
         14 . The isolated monoclonal antibody of  claim 2 , which is a human antibody. 
     
     
         15 . The isolated monoclonal antibody of  claim 2 , which is an IgG molecule. 
     
     
         16 . The isolated monoclonal antibody of  claim 15 , which is an IgG1 molecule. 
     
     
         17 . The isolated monoclonal antibody of  claim 14 , which is a germlined antibody. 
     
     
         18 . The isolated monoclonal antibody of  claim 2 , which is substantially a full-length antibody. 
     
     
         19 . The isolated monoclonal antibody of  claim 2 , which comprises an antigen-binding fragment of a full-length antibody. 
     
     
         20 . The isolated monoclonal antibody of  claim 2 , which comprises a heavy chain variable region and a light chain variable region. 
     
     
         21 . A pharmaceutical composition, comprising the monoclonal antibody of  claim 2  and a pharmaceutically acceptable carrier. 
     
     
         22 . A method for treating hereditary angioedema, comprising administering to a subject in need thereof an effective amount of the monoclonal antibody of  claim 2 .

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