IP Library Granted Patent US 7,879,984
Granted Patent B2
US 7,879,984 · App. 12/183,274 · Granted Feb 1, 2011

Human antibodies to human CD20 and method of using thereof

Assignee: Regeneron Pharmaceuticals, Inc.
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Quick Facts
Patent No.
US 7,879,984
App. No.
12/183,274
Granted
Feb 1, 2011
Kind
B2
Abstract

A human antibody or antigen-binding fragment of an antibody that specifically binds human CD20 and is capable of inducing complement dependent cytotoxicity (CDC), and is capable of increasing symptom free survival time between about 2-fold to about 9-fold or more, relative to control-treated animals in a mouse model of human lymphoma. The antibody or antigen-binding fragment thereof is useful in a therapeutic method for treating a CD20-mediated disease or condition, such as for example, non-Hodgkin's lymphoma, rheumatoid arthritis, systemic lupus erythematosus, Crohn's disease, chronic lymphocytic leukemia, and inflammatory diseases.

Claims (10)

1. A human antibody or antigen-binding fragment of an antibody that specifically binds human CD20 and is capable of inducing complement dependent cytotoxicity (CDC), wherein the antibody or antibody fragment comprises:

(i) a heavy chain complementarity determining region 1 (HCDR1) having the amino acid sequence of SEQ ID NO:341;

(ii) a heavy chain complementarity determining region 2 (HCDR2) having the amino acid sequence of SEQ ID NO:343;

(iii) a heavy chain complementarity determining region 3 (HCDR3) having the amino acid sequence of SEQ ID NO:345;

(iv) a light chain complementarity determining region 1 (LCDR1) having the amino acid sequence of SEQ ID NO:349;

(v) a light chain complementarity determining region 2 (LCDR2) having the amino acid sequence of SEQ ID NO:351; and

(vi) a light chain complementarity determining region 3 (LCDR3) having the amino acid sequence of SEQ ID NO:353.

2. The antibody or fragment thereof of claim 1 , wherein the antibody or fragment thereof exhibits an EC 50 0.2 nM or less as measured in Daudi cells, or an EC 50 of 0.4 nM or less as measured by RL cells.

3. The antibody or fragment thereof of claim 1 , wherein the antibody or fragment thereof is capable of increasing symptom free survival time between about 2-fold to about 9-fold or more, relative to control-treated animals in a mouse model of human lymphoma.

4. The antibody or antigen-binding fragment thereof of claim 1 , wherein the antibody or fragment thereof comprises a HCVR having the amino acid sequence of SEQ ID NO:339, and a LCVR having the amino acid sequence of SEQ ID NO:347.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 4, 2008
From: MARTIN, JOEL H.; WANG, LI-HSIEN; STEVENS, SEAN; ALLISON, ERIN M.
To: REGENERON PHARMACEUTICALS, INC.
Reel/Frame 021347/0377 →
Continuity (3)
Provisional Application 6096281100 · Jul 31, 2007
Provisional Application 6106799400 · Mar 3, 2008
Related Publication 20090035322A1 · Feb 5, 2009