IP Library Granted Patent US 9,382,320
Granted Patent B2
US 9,382,320 · App. 14/656,431 · Granted Jul 5, 2016

Humanized and chimeric monoclonal antibodies to CD47

Inventors: Jie Liu (Palo Alto, CA); Irving L. Weissman (Stanford, CA); Ravindra Majeti (Stanford, CA)
Assignee: THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY
C07K16/2803C07K16/2896G01N33/6872C07K2317/24C07K2317/70C07K2317/76
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Quick Facts
Patent No.
US 9,382,320
App. No.
14/656,431
Granted
Jul 5, 2016
Kind
B2
Abstract

Humanized or chimeric anti-CD47 monoclonal antibodies are provided. The antibodies bind to and neutralize human CD47, and find use in various therapeutic methods. Preferred are non-activating antibodies. Embodiments of the invention include isolated antibodies and derivatives and fragments thereof, pharmaceutical formulations comprising one or more of the humanized or chimeric anti-CD47 monoclonal antibodies; and cell lines that produce these monoclonal antibodies. Also provided are amino acid sequences of the antibodies.

Claims (9)

1. A method of increasing phagocytosis of a cancer cell expressing CD47 in a human subject, the method comprising:

administering to the human subject a therapeutically effective dose of a chimeric or humanized antibody that specifically binds to human CD47 comprising a variable heavy (VH) region containing the VH complementarity regions, CDR1, CDR2 and CDR3, respectively set forth in SEQ ID NO:20, 21 and 22; and a variable light (VL) region containing the VL complementary regions, CDR1, CDR2 and CDR3, respectively set forth in SEQ ID NO:23, 24 and 25.

2. The method of claim 1 , wherein said variable light (VL) region comprises the amino acid sequence selected from the group consisting of the SEQ ID NO:41, SEQ ID NO: 42 and SEQ ID NO: 43.

3. The method of claim 1 , wherein said variable heavy (VH) region comprises the amino acid sequence selected from the group consisting of the SEQ ID NO:36, SEQ ID NO: 37 and SEQ ID NO: 38.

4. The method of claim 1 , wherein the antibody does not activate CD47 upon binding.

5. The method of claim 1 , wherein the antibody is a humanized monoclonal antibody.

6. The method of claim 1 , wherein the antibody is a chimeric antibody.

7. The method of claim 1 , wherein the antibody comprises a human IgG4 constant region.

8. The method of claim 1 , further comprising administering an additional FcR-engaging antibody specific for an additional surface antigen on a targeted cancer cell.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 16, 2015
From: LIU, JIE; WEISSMAN, IRVING L.; MAJETI, RAVINDRA
To: THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY
Reel/Frame 035174/0848 →
Continuity (4)
Division 13675274 · Nov 13, 2012
Continuation In Part PCTUS2011036535 · May 13, 2011
Provisional Application 61395652 · May 14, 2010
Related Publication 20150183874A1 · Jul 2, 2015