US2012064066A1PendingUtilityA1
Monoclonal Antibodies to Hepatocyte Growth Factor
Est. expiryApr 18, 2023(expired)· nominal 20-yr term from priority
A61P 43/00A61P 35/00A61P 35/04A61P 1/16C07K 2317/76A61K 2039/505G01N 2333/4753C07K 2317/92C07K 16/22C07K 2317/73A61K 39/395C07K 16/00
55
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
The present invention is directed toward a neutralizing monoclonal antibody to hepatocyte growth factor, a pharmaceutical composition comprising same, and methods of treatment comprising administering such a pharmaceutical composition to a patient.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A monoclonal antibody (mAb) that binds and neutralizes human Hepatocyte Growth Factor (HGF).
2 . The mAb of claim 1 which is chimeric.
3 . The mAb of claim 1 which is humanized.
4 . The mAb of claim 1 which is human.
5 . The mAb of claim 1 which inhibits binding of HGF to cMet by at least 50%.
6 . The mAb of claim 1 which inhibits HGF-induced scattering of Madin-Darby canine kidney cells.
7 . The mAb of claim 1 which inhibits HGF-induced angiogenesis.
8 . The mAb of claim 1 which neutralizes all biological activities of HGF.
9 . The mAb of claim 1 which inhibits growth of a human tumor xenograft in a mouse.
10 . The mAb of claim 9 which completely inhibits growth of a human tumor xenograft in a mouse.
11 . The mAb of claim 1 which is a Fab or F(ab′) 2 fragment or single-chain antibody.
12 . The mAb of claim 1 which specifically binds HGF with a binding affinity of at least 10 8 M −1 .
13 . A chimeric or humanized L2G7 mAb.
14 . An antibody that competes for binding to human HGF with an antibody of claim 13 .
15 . A cell line producing a mAb of claim 1 .
16 . A pharmaceutical composition comprising a mAb of claim 13 .
17 . A method of treating cancer in a patient comprising administering to the patient a pharmaceutical composition comprising a neutralizing anti-HGF mAb.
18 . A method of claim 17 wherein said cancer is glioblastoma.
19 . The method of claim 17 wherein said mAb is a chimeric or humanized L2G7 mAb.Cited by (0)
No later patents cite this yet.
References (0)
No backward citations on record.