IP Library › Granted Patent US 11,098,126
Granted Patent B2
US 11,098,126 · App. 16/313,710 · Granted Aug 24, 2021

Anti-MET antibodies and uses thereof

Inventor: Paolo Michieli (Rivalta di Torino, IT)
Assignee: AGOMAB THERAPEUTICS BVBA
C07K16/2863A61P1/04A61P1/16A61P3/10A61P13/12A61P29/00A61K2039/505C07K2317/21C07K2317/22C07K2317/24C07K2317/33C07K2317/34C07K2317/51C07K2317/515C07K2317/522C07K2317/524C07K2317/526C07K2317/528C07K2317/53C07K2317/55C07K2317/565C07K2317/567C07K2317/74C07K2317/75C07K2317/92C07K2317/94
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Quick Facts
Patent No.
US 11,098,126
App. No.
16/313,710
Granted
Aug 24, 2021
Kind
B2
Abstract

The invention relates to agonistic anti-MET antibodies and uses thereof in the therapeutic treatment of disease. The antibodies bind with high affinity to the human and mouse hepatocyte growth factor (HGF) receptor, also known as MET, and are agonists of MET in both humans and mice, producing molecular and cellular effects resembling the effects of HGF binding.

Claims (14)

1. An antibody or antigen binding fragment which comprises:

a heavy chain variable domain comprising H-CDR1, H-CDR2 and H-CDR3, and

a light chain variable domain comprising L-CDR1, L-CDR2 and L-CDR3,

wherein:

H-CDR1 comprises the amino acid sequence shown as SEQ ID NO:30,

H-CDR2 comprises the amino acid sequence shown as SEQ ID NO:32,

H-CDR3 comprises the amino acid sequence shown as SEQ ID NO:34,

L-CDR1 comprises the amino acid sequence shown as SEQ ID NO: 107,

L-CDR2 comprises the amino acid sequence shown as SEQ ID NO: 109, and

L-CDR3 comprises the amino acid sequence shown as SEQ ID NO: 111; and

wherein the antibody or antigen binding fragment binds human MET protein comprising the amino acid sequence of SEQ ID NO: 239.

2. The antibody or antigen binding fragment according to claim 1 ,

wherein the heavy chain variable domain comprises the amino acid sequence of SEQ ID NO: 163, or a sequence at least 90%, 95%, 97% or 99% identical thereto, and the light chain variable domain comprises the amino acid sequence of SEQ ID NO: 164, or a sequence at least 90%, 95%, 97% or 99% identical thereto.

3. A pharmaceutical composition comprising an antibody or antigen binding fragment according to claim 1 and at least one pharmaceutically acceptable carrier or excipient.

Assignments (3)
CHANGE OF ASSIGNEE ADDRESS Recorded Aug 19, 2024
From: AGOMAB THERAPEUTICS
To: AGOMAB THERAPEUTICS
Reel/Frame 069384/0892 →
CHANGE OF NAME Recorded Jul 25, 2022
From: AGOMAB THERAPEUTICS BVBA
To: AGOMAB THERAPEUTICS
Reel/Frame 060855/0961 →
COMBINED DECLARATION AND ASSIGNMENT Recorded Mar 1, 2019
From: MICHIELI, PAOLO
To: AGOMAB THERAPEUTICS BVBA
Reel/Frame 048478/0682 →
Priority Claims (1)
GB 1611123.9 · Jun 27, 2016 · national
Continuity (1)
Related Publication 20190315873A1 · Oct 17, 2019