US2017204193A1PendingUtilityA1

Antibody Fc Mutants with Ablated Effector Functions

Assignee: JANSSEN BIOTECH INCPriority: Nov 30, 2009Filed: Mar 20, 2017Published: Jul 20, 2017
Est. expiryNov 30, 2029(~3.4 yrs left)· nominal 20-yr term from priority
C07K 16/00A61K 39/395C07K 16/28C07K 2/00C07K 16/32C12P 21/00C12N 15/63A61P 9/10A61P 43/00A61P 37/06A61P 37/08A61P 7/04A61P 7/06A61P 9/00A61P 25/28A61P 29/00A61P 19/02A61P 1/04A61P 17/00A61P 11/06A61P 19/00C07K 2317/734C07K 2317/732C07K 2317/71C07K 16/2887A61K 2039/505A61K 38/00C07K 2317/524C07K 2317/73C07K 2317/54C07K 2317/92C07K 2317/52
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Claims

Abstract

Antibody and other Fc-containing molecules with variations in the Fc region reduce binding to Fc gamma receptors and resulting activity and can be used in the treatment of various diseases and disorders.

Claims

exact text as granted — not AI-modified
What is claimed: 
     
         1 . A method for treating a condition in a subject or patient characterized by the migration and concentration of macrophages, comprising administering to the subject or patient an Fc-containing molecule having decreased affinity for at least FcγRI and FcγRIIa as compared to an Fc-containing molecule with a wildtype Fc domain, comprising an antibody Fc domain with a mutated IgG2 constant region comprising the mutations V234A, G237A, P238S, H268A, V309L, A330S and P331S, wherein residue numbering is according to the EU numbering system 
     
     
         2 . The method of  claim 1 , wherein the patient is an unborn infant and the Fc-containing molecule is administered to the mother of the patient. 
     
     
         3 . The method of  claim 1 , wherein the Fc-containing molecule is an antibody or a Fc fusion protein. 
     
     
         4 . The method of  claim 1 , wherein the Fc domain of the Fc-containing molecule with the mutated IgG2 constant region is capable of specifically binding FcRn.

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