Anti-c-Met/anti-Ang2 bispecific antibody

US9808507B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9808507-B2
Application numberUS-201514835376-A
CountryUS
Kind codeB2
Filing dateAug 25, 2015
Priority dateAug 25, 2014
Publication dateNov 7, 2017
Grant dateNov 7, 2017

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

An anti-c-Met/anti-Ang2 bispecific antibody including (a) an anti-c-Met antibody or antigen-binding fragment thereof and (b) an anti-Ang2 antibody or antigen-binding fragment thereof, a pharmaceutical composition including the anti-c-Met/anti-Ang2 bispecific antibody, and a method using the anti-c-Met/anti-Ang2 bispecific antibody.

First claim

Opening claim text (preview).

What is claimed is: 1. An anti-c-Met/anti-Ang2 bispecific antibody comprising (a) an anti-c-Met antibody or antigen-binding fragment thereof and (b) an anti-Ang2 antibody or antigen-binding fragment thereof, wherein the anti-c-Met antibody or antigen-binding fragment thereof comprises (i) a heavy chain variable region comprising (a) a CDR-H1 comprising SEQ ID NO: 1, 22, 23, or 24, (b) a CDR-H2 comprising SEQ ID NO: 2, 25, or 26, and (c) a CDR-H3 comprising SEQ ID NO: 3, 27, 28, or 85, and (ii) a light chain variable region comprising (a) a CDR-L1 comprising an SEQ ID NO: 10, 29, 30, 31, 32, 33 or 106, (b) a CDR-L2 comprising SEQ ID NO: 11, 34, 35, or 36, and (c) a CDR-L3 comprising SEQ ID NO: 12, 13, 14, 15, 16, 37, 86, or 89; and the anti-Ang-2 antibody or antigen-binding fragment thereof comprises: (i) a heavy chain variable region comprising (a) a CDR-H1 comprising SEQ ID NO: 109, (b) a CDR-H2 comprising SEQ ID NO: 128, and (c) a CDR-H3 comprising SEQ ID NO: 111, and (ii) a light chain variable region comprising a CDR-L1 comprising SEQ ID NO: 129, a CDR-L2 comprising SEQ ID NO: 130, and a CDR-L3 comprising SEQ ID NO: 131. 2. The anti-c-Met/anti-Ang2 bispecific antibody of claim 1 , wherein the anti-Ang2 antibody or antigen-binding fragment thereof comprises: a heavy chain variable region comprising a CDR-H1 comprising SEQ ID NO: 109, a CDR-H2 comprising SEQ ID NO: 110, and a CDR-H3 comprising SEQ ID NO: 111; and a light chain variable region comprising a CDR-L1 comprising SEQ ID NO: 112, a CDR-L2 comprising SEQ ID NO: 113, and a CDR-L3 comprising SEQ ID NO: 114. 3. The anti-c-Met/anti-Ang2 bispecific antibody of claim 2 , wherein the anti-Ang2 antibody or antigen-binding fragment thereof comprises a heavy chain variable region comprising SEQ ID NO: 115 and a light chain variable region comprising SEQ ID NO: 117. 4. The anti-c-Met/anti-Ang2 bispecific antibody of claim 1 , wherein the anti-Ang2 antibody or antigen-binding fragment thereof comprises: a heavy chain variable region comprising a CDR-H1 comprising SEQ ID NO: 109, a CDR-H2 comprising SEQ ID NO: 128, and a CDR-H3 comprising SEQ ID NO: 111; and a light chain variable region comprising a CDR-L1 comprising SEQ ID NO: 129, a CDR-L2 comprising SEQ ID NO: 130, and a CDR-L3 comprising SEQ ID NO: 131, with the proviso that an anti-Ang2 antibody or an antigen-binding fragment thereof does not comprise a heavy chain variable region comprising a CDR-H1 of SEQ ID NO: 109, a CDR-H2 of SEQ ID NO: 110, and a CDR-H3 of SEQ ID NO: 111, and a light chain variable region comprising a CDR-L1 of SEQ ID NO: 112, a CDR-L2 of SEQ ID NO: 113, and a CDR-L3 of SEQ ID NO: 114. 5. The anti-c-Met/anti-Ang2 bispecific antibody of claim 4 , wherein the anti-Ang2 antibody or antigen-binding fragment thereof comprises: a heavy chain variable region comprising a CDR-H1 comprising SEQ ID NO: 109, a CDR-H2 comprising SEQ ID NO: 122 or 123, and a CDR-H3 comprising SEQ ID NO: 111; and a light chain variable region comprising a CDR-L1 comprising SEQ ID NO: 112, 124, or 125, a CDR-L2 comprising SEQ ID NO: 113 or 126, and a CDR-L3 comprising SEQ ID NO: 114 or 127, with the proviso that an anti-Ang2 antibody or an antigen-binding fragment thereof does not comprise a heavy chain variable region comprising a CDR-H1 of SEQ ID NO: 109, a CDR-H2 of SEQ ID NO: 110, and a CDR-H3 of SEQ ID NO: 111, and a light chain variable region comprising a CDR-L1 of SEQ ID NO: 112, a CDR-L2 of SEQ ID NO: 113, and a CDR-L3 of SEQ ID NO: 114. 6. The anti-c-Met/anti-Ang2 bispecific antibody of claim 5 , wherein the anti-Ang2 antibody or antigen-binding fragment thereof comprises: a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 160, 161, 162, 163, or 164, and a light chain variable region comprising the amino acid sequence of SEQ ID NO: 165, 166, 167, 168, 169, 170, or 171. 7. The anti-c-Met/anti-Ang2 bispecific antibody of claim 1 , wherein the anti-c-Met antibody or antigen-binding fragment thereof comprises: a heavy chain variable region comprising SEQ ID NO: 17, 74, 87, 90, 91, 92, 93, or 94; and a light chain variable region comprising SEQ ID NO: 196, 18, 19, 20, 21, 75, 88, 95, 96, 97, 98, 99, or 107. 8. A recombinant nucleic acid encoding the anti-c-Met/anti-Ang2 bispecific antibody of claim 1 . 9. The recombinant nucleic acid of claim 8 , wherein the recombinant nucleic acid is in an isolated vector. 10. The recombinant nucleic acid of claim 8 , wherein the recombinant nucleic acid is in an isolated cell. 11. A method of preparing an anti-c-Met/anti-Ang2 bispecific antibody of claim 1 by expressing a nucleic acid encoding the anti-c-Met/anti-Ang2 bispecific antibody in a cell and isolating the bispecific antibody from the cell. 12. A method of treating a disease associated with overexpression of c-Met or Ang2 in a subject, comprising administering the anti-c-Met/anti-Ang2 bispecific antibody of claim 1 to the subject, wherein the disease associated with overexpression of c-Met or Ang2 is lung cancer, gastric cancer, or ovarian cancer. 13. The method of claim 12 , further comprising administering Ang2 to the subject.

Assignees

Inventors

Classifications

  • C07K16/22Primary

    against growth factors {; against growth regulators} · CPC title

  • multispecific · CPC title

  • Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation · CPC title

  • containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered · CPC title

  • A61K38/18Primary

    Growth factors; Growth regulators · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US9808507B2 cover?
An anti-c-Met/anti-Ang2 bispecific antibody including (a) an anti-c-Met antibody or antigen-binding fragment thereof and (b) an anti-Ang2 antibody or antigen-binding fragment thereof, a pharmaceutical composition including the anti-c-Met/anti-Ang2 bispecific antibody, and a method using the anti-c-Met/anti-Ang2 bispecific antibody.
Who is the assignee on this patent?
Samsung Electronics Co Ltd
What technology area does this patent fall under?
Primary CPC classification C07K16/22. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Nov 07 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).