IP Library Granted Patent US 9,475,875
Granted Patent B2
US 9,475,875 · App. 14/643,886 · Granted Oct 25, 2016

Anti-EGFRvIII antibodies and uses thereof

Inventors: Jessica R. Kirshner (New York, NY); Douglas MacDonald (New York, NY); Gavin Thurston (Briarcliff Manor, NY); Joel H. Martin (Putnam Valley, NY); Frank Delfino (Poughquag, NY); Thomas Nittoli (Pearl River, NY); Marcus Kelly (New York, NY)
Assignee: REGENERON PHARMACEUTICALS, INC.
C07K16/2863A61K39/39558A61K45/06A61K47/48384A61K47/48569A61K2039/505A61K2039/507C07K2317/33C07K2317/34C07K2317/565C07K2317/77C07K2317/92
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Quick Facts
Patent No.
US 9,475,875
App. No.
14/643,886
Granted
Oct 25, 2016
Kind
B2
Abstract

The present invention provides antibodies that bind to the class III variant of EGFR (EGFRvIII) and methods of using the same. According to certain embodiments, the antibodies of the invention bind human EGFRvIII with high affinity. The antibodies of the invention may be fully human antibodies. The invention includes anti-EGFRvIII antibodies conjugated to a cytotoxic agent, radionuclide, or other moiety detrimental to cell growth or proliferation. The antibodies of the invention are useful for the treatment of various cancers.

Claims (9)

1. An isolated antibody or antigen-binding fragment thereof that specifically binds human EGFRvIII, wherein the antibody or fragment thereof comprises a heavy chain variable region (HCVR) and a light chain variable region (LCVR), and wherein the HCVR comprises three complementarity determining regions (CDRs), HCDR1, HCDR2 and HCDR3, contained in the amino acid sequence of SEQ ID NO:34 and the LCVR comprises three CDRs, LCDR1, LCDR2 and LCDR3, contained in the amino acid sequence of SEQ ID NO:42.

2. The antibody or antigen-binding fragment of claim 1 , wherein the antibody or antigen-binding fragment is conjugated to a cytotoxin.

3. The antibody or antigen-binding fragment of claim 2 , wherein the cytotoxin is selected from the group consisting of biotoxins, chemotherapeutic agents and radioisotopes.

4. The antibody or antigen-binding fragment of claim 2 , wherein the cytotoxin is selected from the group consisting of maytansinoids, auristatins, tomaymycins, duocarmycins, 225Ac, 227Th, and any derivatives thereof.

5. A pharmaceutical composition comprising the antibody or antigen-binding fragment of claim 1 , and a pharmaceutically acceptable carrier.

6. The pharmaceutical composition of claim 5 , further comprising one or more additional therapeutic agents selected from the group consisting of a chemotherapeutic agent, anti-inflammatory agents, and analgesics.

7. The antibody or antigen-binding fragment of claim 1 , wherein the HCVR comprises an amino acid sequence of SEQ ID NO: 34.

8. The antibody or antigen-binding fragment of claim 1 , wherein the LCVR comprises an amino acid sequence of SEQ ID NO: 42.

9. The antibody or antigen-binding fragment of claim 1 , wherein the antibody or antigen-binding fragment comprises a HCVR/LCVR sequence pair of SEQ ID NO:34/42.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 28, 2016
From: KIRSHNER, JESSICA R.; MACDONALD, DOUGLAS; THURSTON, GAVIN; MARTIN, JOEL H.; DELFINO, FRANK; NITTOLI, THOMAS; KELLY, MARCUS
To: REGENERON PHARMACEUTICALS, INC.
Reel/Frame 037629/0523 →
Continuity (2)
Provisional Application 61950963 · Mar 11, 2014
Related Publication 20150259423A1 · Sep 17, 2015