IP Library › Granted Patent US 9,150,655
Granted Patent B2
US 9,150,655 · App. 13/818,283 · Granted Oct 6, 2015

Anti-C-met antibody and methods of use thereof

Inventors: Han-Chung Wu (Taipei, TW); Ruei-Min Lu (Sanchong, TW)
Assignees: ACADEMIA SINICA; Chi-Ming Liang
C07K16/2869A61K9/0019A61K9/1271A61K47/24A61K47/48823A61K49/0058A61K49/0067C07K16/2863A61K2039/505C07K2317/622C07K2317/77C07K2317/92C07K2319/30
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,150,655
App. No.
13/818,283
Granted
Oct 6, 2015
Kind
B2
Abstract

Antibodies that bind to c-Met are provided herein, as well as related compositions and methods of use. Methods of use encompass cancer therapies and diagnostics. In certain embodiments, antibodies bind mammalian cell surface antigen (e.g., cancer cell surface antigen). The antibodies can also be endocytosed upon binding to cells. Cells that can be targeted by the antibodies include carcinomas, such as those in lung, kidney, liver, stomach, breast, and brain, etc.

Claims (24)

1. An isolated monoclonal antibody that binds to human c-Met, comprising:

a heavy chain variable region wherein the variable region comprises as a CDR1 the sequence of SEQ ID NO:10; as a CDR2 the sequence of SEQ ID NO:12, and as a CDR3 the sequence of SEQ ID NO:22; and

a light chain variable region wherein the variable region comprises as a CDR1 the sequence of SEQ ID NO:31, as a CDR2 the sequence of SEQ ID NO:33, and as a CDR3 the sequence of SEQ ID NO:43.

2. The isolated monoclonal antibody of claim 1 , wherein said antibody comprises a) a full length VH of clone 1, comprising SEQ ID NO:9 joined to SEQ ID NO:10 joined to SEQ ID NO:11 joined to SEQ ID NO:12 joined to SEQ ID NO:21 joined to SEQ ID NO:22 joined to SEQ ID NO:23; and b) a full length VL of clone 1 comprising SEQ ID NO:30 joined to SEQ ID NO:31 joined to SEQ ID NO:32 joined to SEQ ID NO:33 joined to SEQ ID NO:42 joined to SEQ ID NO:43 joined to SEQ ID NO:44.

3. An isolated monoclonal antibody that binds to human c-Met comprising:

a heavy chain variable region wherein the variable region comprises as a CDR1 the sequence of SEQ ID NO:14; as a CDR2 the sequence of SEQ ID NO:16, and as a CDR3 the sequence of SEQ ID NO:25; and

a light chain variable region wherein the variable region comprises as a CDR1 the sequence of SEQ ID NO:35; as a CDR2 the sequence of SEQ ID NO:37, and as a CDR3 the sequence of SEQ ID NO:46.

4. The isolated monoclonal antibody of claim 3 , wherein said antibody comprises a) a full length VH of clone 20 comprising SEQ ID NO:13 joined to SEQ ID NO:14 joined to SEQ ID NO:15 joined to SEQ ID NO:16 joined to SEQ ID NO:24 joined to SEQ ID NO:25 joined to SEQ ID NO:26; and b) a full length VL of clone 20 comprising SEQ ID NO:34 joined to SEQ ID NO:35 joined to SEQ ID NO:36 joined to SEQ ID NO:37 joined to SEQ ID NO:45 joined to SEQ ID NO:46 joined to SEQ ID NO:47.

5. The isolated monoclonal antibody of claim 3 that, when bound to c-Met on the surface of a living mammalian cell, is endocytosed by the cell.

6. The isolated monoclonal antibody of claim 3 , wherein said anybody is a single chain Fv (scFv), IgG, Fab, (Fab′)2, or (scFv′)2.

7. The isolated monoclonal antibody of claim 3 , wherein said antibody is labeled.

8. The isolated monoclonal antibody of claim 3 , wherein said antibody is conjugated to an anti-cancer agent.

9. A lipidic nanoparticle comprising a surface and an interior space, said interior space comprising an anti-cancer agent, wherein an isolated monoclonal antibody of claim 3 is attached to the surface of said lipidic nanoparticle.

10. The lipidic nanoparticle of claim 9 , wherein when the lipidic nanoparticle is contacted with a cell expressing cell surface c-Met, said antibody binds to the cell surface c-Met and the lipidic nanoparticle is endocytosed.

11. A composition comprising:

a pharmaceutically acceptable carrier; and

an isolated monoclonal antibody of claim 3 .

12. The composition of claim 11 , wherein said composition is formulated for parenteral administration.

13. The composition of claim 11 , wherein said composition is formulated for intravenous, intrathecal, or intraventricular administration.

14. A kit comprising a composition of claim 11 .

15. An isolated monoclonal antibody that binds to human c-Met comprising:

a heavy chain variable region wherein the variable region comprises as a CDR1 the sequence of SEQ ID NO:18; as a CDR2 the sequence of SEQ ID NO:20, and as a CDR3 the sequence of SEQ ID NO:28;

and a light chain variable region wherein the variable region comprises as a CDR1 the sequence of SEQ ID NO:39; as a CDR2 the sequence of SEQ ID NO:41, and as a CDR3 the sequence of SEQ ID NO:49.

16. The isolated monoclonal antibody of claim 15 , wherein said antibody comprises: a) a full length VH of clone 21 comprising SEQ ID NO:17 joined to SEQ ID NO:18 joined to SEQ ID NO:19 joined to SEQ ID NO:20 joined to SEQ ID NO:27 joined to SEQ ID NO:28 joined to SEQ ID NO:29; and b) a full length VL of clone 21 comprising SEQ ID NO:38 joined to SEQ ID NO:39 joined to SEQ ID NO:40 joined to SEQ ID NO:41 joined to SEQ ID NO:48 joined to SEQ ID NO:49 joined to SEQ ID NO:50.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 29, 2013
From: WU, HAN-CHUNG; LU, RUEI-MIN
To: ACADEMIA SINICA; LIANG, CHI-MING
Reel/Frame 030310/0811 →
Continuity (2)
Provisional Application 61402788 · Sep 3, 2010
Related Publication 20130209365A1 · Aug 15, 2013