IP Library Granted Patent US 9,889,206
Granted Patent B2
US 9,889,206 · App. 14/485,062 · Granted Feb 13, 2018

C-Met targeting compound-bioactive material conjugate and use thereof

Inventors: Su Young Chae (Suwon-si, KR); Sunghyun Kim (Hwaseong-si, KR); Eun Ko (Anyang-si, KR); Yun Ju Jeong (Hwaseong-si, KR); Jae Hyun Choi (Seongnam-si, KR)
Assignee: SAMSUNG ELECTRONICS CO., LTD.
A61K47/48569A61K47/486A61K47/48384
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Quick Facts
Patent No.
US 9,889,206
App. No.
14/485,062
Granted
Feb 13, 2018
Kind
B2
Abstract

Disclosed is a conjugate in which a c-Met targeting compound and a bioactive material are chemically conjugated with each other, and methods of use thereof.

Claims (26)

1. A method of treating a cancer, comprising administering an antibody-drug conjugate comprising an anti-c-Met antibody and a cytotoxic agent, in which the anti-c-Met antibody and the cytotoxic agent are conjugated with each other, to a subject in need of cancer treatment,

wherein the anti-c-Met antibody binds to an epitope comprising a sequence of 5 to 19 consecutive amino acids of SEQ ID NO: 71 including the amino acid sequence EEPSQ (SEQ ID NO: 73) and comprises:

a CDR-H1 comprising the amino acid sequence of SEQ ID NO: 1, 22, 23, or 24;

a CDR-H2 comprising the amino acid sequence of SEQ ID NO: 2, 25, or 26;

a CDR-H3 comprising the amino acid sequence of SEQ ID NO: 3, 27, 28, or 85;

a CDR-L1 comprising the amino acid sequence of SEQ ID NO: 10, 29, 30, 31, 32, 33, or 106;

a CDR-L2 comprising the amino acid sequence of SEQ ID NO: 11, 34, 35, or 36; and

a CDR-L3 comprising the amino acid sequence of SEQ ID NO: 13, 14, 15, 16, or 37.

2. The method of claim 1 , wherein the anti-c-Met antibody binds to an epitope of SEQ ID NO: 71, SEQ ID NO: 72, or SEQ ID NO: 73.

3. The method of claim 1 , wherein the anti-c-Met antibody comprises:

a CDR-H1 comprising the amino acid sequence of SEQ ID NO: 1; a CDR-H2 comprising the amino acid sequence of SEQ ID NO: 2; a CDR-H3 comprising the amino acid sequence of SEQ ID NO: 3;

a CDR-L1 comprising the amino acid sequence of SEQ ID NO: 10, a CDR-L2 comprising the amino acid sequence of SEQ ID NO: 11; and a CDR-L3 comprising the amino acid sequence of SEQ ID NO: 13, 14, 15, or 16.

4. The method of claim 1 , wherein the cytotoxic agent is at least one selected from the group consisting of maytansine, auristatin based drug, calicheamycin based drug, pyrrolobenzodiazepine based drug, duocarmycin, docetaxel, doxorubicin, carboplatin, cisplatin, cyclophosphamide, ifosfamide, nidran, nitrogen mustard, mechlorethamine HCl, bleomycin, mitomycin C, cytarabine, fluorouracil, gemcitabine, trimetrexate, methotrexate, etoposide, vinblastine, vinorelbine, alimta, altretamine, procarbazine, paclitaxel, taxotere, topotecan, irinotecan, and a radio-isotope.

5. A method for delivering a cytotoxic agent into a cell, comprising administering an antibody-drug conjugate comprising an anti-c-Met antibody and a cytotoxic agent, in which the anti-c-Met antibody and the cytotoxic agent are conjugated with each other, to a subject in need of intracellular delivery of the cytotoxic agent,

wherein the anti-c-Met antibody binds to an epitope comprising a sequence of 5 to 19 consecutive amino acids of SEQ ID NO: 71 including the amino acid sequence EEPSQ (SEQ ID NO: 73) and comprises:

a CDR-H1 comprising the amino acid sequence of SEQ ID NO: 1, 22, 23, or 24;

a CDR-H2 comprising the amino acid sequence of SEQ ID NO: 2, 25, or 26;

a CDR-H3 comprising the amino acid sequence of SEQ ID NO: 3, 27, 28, or 85;

a CDR-L1 comprising the amino acid sequence of SEQ ID NO: 10, 29, 30, 31, 32, 33, or 106;

a CDR-L2 comprising the amino acid sequence of SEQ ID NO: 11, 34, 35, or 36; and

a CDR-L3 comprising the amino acid sequence of SEQ ID NO: 13, 14, 15, 16, or 37.

6. The method of claim 5 , wherein the anti-c-Met antibody binds to an epitope of SEQ ID NO: 71, SEQ ID NO: 72, or SEQ ID NO: 73.

7. The method of claim 5 , wherein the anti-c-Met antibody comprises:

a CDR-H1 comprising the amino acid sequence of SEQ ID NO: 1; a CDR-H2 comprising the amino acid sequence of SEQ ID NO: 2; a CDR-H3 comprising the amino acid sequence of SEQ ID NO: 3;

a CDR-L1 comprising the amino acid sequence of SEQ ID NO: 10, a CDR-L2 comprising the amino acid sequence of SEQ ID NO: 11; and a CDR-L3 comprising the amino acid sequence of SEQ ID NO: 13, 14, 15, or 16.

8. The method of claim 5 , wherein the cytotoxic agent is at least one selected from the group consisting of maytansine, auristatin based drug, calicheamycin based drug, pyrrolobenzodiazepine based drug, duocarmycin, docetaxel, doxorubicin, carboplatin, cisplatin, cyclophosphamide, ifosfamide, nidran, nitrogen mustard, mechlorethamine HCl, bleomycin, mitomycin C, cytarabine, fluorouracil, gemcitabine, trimetrexate, methotrexate, etoposide, vinblastine, vinorelbine, alimta, altretamine, procarbazine, paclitaxel, taxotere, topotecan, irinotecan, and a radio-isotope.

Assignments (3)
NUNC PRO TUNC ASSIGNMENT Recorded Mar 11, 2026
From: SAMSUNG ELECTRONICS CO., LTD.
To: SAMSUNG BIOLOGICS CO., LTD.
Reel/Frame 074033/0938 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 21, 2019
From: VAN DER BLOM, NICOLAAS
To: NVB WINDMILL ENERGY INTERNATIONAL LTD
Reel/Frame 050769/0799 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 12, 2014
From: CHAE, SU YOUNG; KIM, SUNGHYUN; KO, EUN; JEONG, YUN JU; CHOI, JAE HYUN
To: SAMSUNG ELECTRONICS CO., LTD.
Reel/Frame 033732/0537 →
Priority Claims (1)
KR 10-2013-0109889 · Sep 12, 2013 · national
Continuity (1)
Related Publication 20150071950A1 · Mar 12, 2015