Monoclonal antibodies against c-met

Abstract

Isolated monoclonal antibodies which bind to human c-Met, the hepatocyte growth factor receptor, and related antibody-based compositions and molecules, are disclosed. Pharmaceutical compositions comprising the antibodies and therapeutic and diagnostic methods for using the antibodies are also disclosed.

1 - 29 . (canceled) 
     
     
         30 . A method of treating cancer comprising administering an effective amount of an antibody which binds human c-Met and comprises a VH region comprising the CDR1, 2 and 3 sequences of SEQ ID NOs: 194, 195, and 196, and a VL region comprising the CDR1, 2 and 3 sequences of SEQ ID NOs: 209, 210, and 104. 
     
     
         31 . The method of  claim 30 , wherein the antibody comprises the CDR1, 2 and 3 sequences of SEQ ID NOs: 98, 99, and 100, and a VL region comprising the CDR1, 2 and 3 sequences of SEQ ID NOs: 102, 103, and 104. 
     
     
         32 . A method of treating cancer comprising administering an effective amount of an antibody which binds human c-Met and comprises heavy and light chain variable regions, wherein the VH region comprises the sequence of SEQ ID NO: 97 and the VL region comprises the sequence of SEQ ID NO: 101. 
     
     
         33 . The method of  claim 30 , wherein the antibody binds to the SEMA domain of c-Met, wherein the antibody inhibits binding of HGF to the SEMA domain with an IC50 of less than 10 μg/mL as determined by time resolved-fluorescent resonance energy transfer (TR-FRET). 
     
     
         34 . The method of  claim 30 , wherein the antibody binds to A431 cells with an EC50 of 10 nM or less, as determined by FACS. 
     
     
         35 . The method of  claim 30 , wherein the antibody is a bivalent antibody. 
     
     
         36 . The method of  claim 30 , wherein the antibody binds to c-Met with an affinity constant (K D ) of 20 nM or less, as determined by bio-layer interferometry. 
     
     
         37 . The method of  claim 30 , wherein the antibody binds to Rhesus monkey c-Met, wherein the signal of antibody binding to Rhesus monkey c-Met is at least 5 times that of a negative control antibody, as determined by FACS. 
     
     
         38 . The method of  claim 30 , wherein the antibody inhibits binding of HGF to the extracellular domain of c-Met, wherein the antibody inhibits binding more than 40%, as determined by ELISA. 
     
     
         39 . The method of  claim 30 , wherein the antibody is capable to inhibit the viability of KP4 cells, wherein the antibody inhibits the viability of KP4 cells by more than 10% after applying 66.7 nM of the antibody to 10,000 KP4 cells for 3 days. 
     
     
         40 . The method of  claim 30 , wherein the antibody is a full-length antibody. 
     
     
         41 . The method of  claim 30 , wherein the antibody is conjugated to another moiety. 
     
     
         42 . The method of  claim 30 , wherein the antibody is an effector-function-deficient antibody. 
     
     
         43 . The method of  claim 30 , wherein the antibody is a monovalent antibody. 
     
     
         44 . The method of  claim 43 , wherein the monovalent antibody further comprises a C H  region of an immunoglobulin or a fragment thereof comprising the C H 2 and C H 3 regions, wherein the C H  region or fragment thereof has been modified such that the region corresponding to the hinge region and, if the immunoglobulin is not an IgG4 subtype, other regions of the C H  region do not comprise any amino acid residues, which are capable of forming disulfide bonds with an identical C H  region or other covalent or stable non-covalent inter-heavy chain bonds with an identical C H  region in the presence of polyclonal human IgG. 
     
     
         45 . The method of  claim 44 , wherein the immunoglobulin is of the IgG4 subtype. 
     
     
         46 . The method of  claim 44 , wherein the heavy chain has been modified such that the entire hinge has been deleted. 
     
     
         47 . The method of  claim 30 , wherein the antibody has been modified to make it less flexible in the hinge region, wherein the hinge region has been modified by:
 (i) deleting the hinge region of the sequence EPKSCDKTHTCPPCP (SEQ ID NO: 214) and substituting it with the IgG2 hinge region of the sequence: ERKCCVECPPCP (SEQ ID NO: 215);   (ii) deleting position 220 so the modified hinge region has the sequence of EPKSDKTHTCPPCP (SEQ ID NO: 216);   (iii) substituting cysteine at position 220 with any other natural amino acid (X) so the modified hinge region has the sequence of EPKSXDKTHTCPPCP (SEQ ID NO: 217);   (iv) deleting the hinge region of sequence EPKSCDKTHTCPPCP (SEQ ID NO: 214);   (v) deleting the hinge region of the sequence EPKSCDKTHTCPPCP (SEQ ID NO: 214) and substituting it with the IgG3 hinge region of the sequence ELKTPLGDTTHTCPRCPEPKSCDTPPPCPRCPEPKSCDTPPPCPRCPEPKSCDTPPPCPRCP (SEQ ID NO: 218); or   (vi) substituting threonine at position 223 with cysteine, and deleting lysine at position 222 and threonine at position 225, so the modified hinge region has the sequence of EPKSCDCHCPPCP (SEQ ID NO: 219),   wherein the amino acid positions are based on the EU index as described in Kabat.   
     
     
         48 . The method of  claim 47 , wherein the hinge region has been modified by substituting cysteine at position 220 with serine so the modified hinge region has the sequence of EPKSSDKTHTCPPCP (SEQ ID NO: 220). 
     
     
         49 . The method of  claim 48 , wherein the antibody is of the IgG2 subtype. 
     
     
         50 . The method of  claim 30 , wherein the antibody has been modified to reduce core-fucosylation below 10%, as determined by high performance anion-exchange chromatography coupled with pulsed amperometric detection. 
     
     
         51 . The method of  claim 30 , wherein the antibody is a bispecific antibody, comprising a c-Met binding site and a second antigen-binding site having a different binding specificity. 
     
     
         52 . The method of  claim 30 , wherein the cancer is selected from the group consisting of: bladder cancer, breast cancer, cervical cancer, cholangiocarcinoma, colorectal cancer, endometrial cancer, esophogeal cancer, gastric cancer, head and neck cancer, kidney cancer, liver cancer, lung cancer, nasopharyngeal cancer, ovarian cancer, pancreatic cancer, gall bladder cancer, prostate cancer, thyroid cancer, osteosarcoma, rhabdomyosarcoma, synovial sarcoma, Kaposi's sarcoma, leiomyosarcoma, malignant fibrous histiocytoma, fibrosarcoma, acute myelogenous leukemia, adult T cell leukemia, chronic myeloid leukemia, lymphoma, multiple myeloma, glioblastoma, astrocytoma, melanoma, mesothelioma, Wilm's tumor, and MiT tumors. 
     
     
         53 . The method of  claim 30 , further comprising administration of one or more further therapeutic agent. 
     
     
         54 . The method of  claim 53 , wherein the therapeutic agent is a chemotherapeutic agent. 
     
     
         55 . A method for inhibiting growth and/or proliferation of a tumor cell expressing c-Met, comprising administration, to an individual in need thereof, of an antibody comprising the CDR1, 2 and 3 sequences of SEQ ID NOs: 194, 195, and 196, and a VL region comprising the CDR1, 2 and 3 sequences of SEQ ID NOs: 209, 210, and 104. 
     
     
         56 . The method of  claim 55 , wherein the antibody comprises the CDR1, 2 and 3 sequences of SEQ ID NOs: 98, 99, and 100, and a VL region comprising the CDR1, 2 and 3 sequences of SEQ ID NOs: 102, 103, and 104.