IP Library › Granted Patent US 11,795,236
Granted Patent B2
US 11,795,236 · App. 16/130,615 · Granted Oct 24, 2023

Method for treating cancer comprising administration of anti-HER2 antibody-drug conjugate

Inventors: Hiroyuki Naito (Tokyo, JP); Yusuke Ogitani (Tokyo, JP); Takeshi Masuda (Tokyo, JP); Takashi Nakada (Tokyo, JP); Masao Yoshida (Tokyo, JP); Shinji Ashida (Tokyo, JP); Koji Morita (Tokyo, JP); Hideki Miyazaki (Tokyo, JP); Yuji Kasuya (Tokyo, JP); Ichiro Hayakawa (Tokyo, JP); Yuki Abe (Tokyo, JP)
Assignee: DAIICHI SANKYO COMPANY, LIMITED
C07K16/32A61K31/4745A61K39/395A61K47/6803A61K47/6849A61K47/6851A61K47/6855A61K47/6857A61K47/6859A61K47/6869C07D491/22C07K16/28C07K16/30C07K16/303C07K16/3015C07K16/3023C07K16/3046C07K16/3069A61K2039/505A61K2039/545C07D491/052C07K2317/24C07K2317/73
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Quick Facts
Patent No.
US 11,795,236
App. No.
16/130,615
Granted
Oct 24, 2023
Kind
B2
Abstract

As an antitumor drug which is excellent in terms of antitumor effect and safety and has an excellent therapeutic effect, there is provided an antibody-drug conjugate in which an antitumor compound represented by the following formula is conjugated to an anti-HER2 antibody via a linker having a structure represented by the following formula: -L 1 -L 2 -L P -NH—(CH 2 )n 1 -L a -(CH 2 )n 2 -C(═O)— wherein the anti-HER2 antibody is connected to the terminal L 1 , and the antitumor compound is connected to the carbonyl group of the —(CH 2 )n 2 -C(═O)— moiety with the nitrogen atom of the amino group at position 1 as the connecting position

Claims (32)

1. A method of treating HER2-low expressing cancer in an individual comprising administering to an individual with HER2-low expressing cancer a drug containing an antibody-drug conjugate or a salt thereof,

wherein the antibody-drug conjugate comprises a linker and an antitumor compound represented by the following formula and anti-HER2 antibody connected to the linker:

-(Succinimid-3-yl-N)—CH 2 CH 2 CH 2 CH 2 CH 2 —C(═O)-GGFG (SEQ ID NO: 3)-NH—CH 2 —O—CH 2 —C(═O)—(NH-DX)

wherein

-(Succinimid-3-yl-N)- has a structure represented by the following formula:

which is connected to the antibody at position 3 thereof and is connected to a methylene group in the linker structure containing this structure on the nitrogen atom at position 1, and

(NH-DX) represents a group represented by the following formula:

wherein the nitrogen atom of the amino group at position 1 is the connecting position, and

wherein the HER2-low expressing cancer is lung cancer, urothelial cancer, colorectal cancer, prostate cancer, ovarian cancer, pancreatic cancer, breast cancer, bladder cancer, gastric cancer, gastrointestinal stromal tumor, uterine cervix cancer, esophageal cancer, squamous cell carcinoma, peritoneal cancer, liver cancer, hepatocellular cancer, colon cancer, rectal cancer, colorectal cancer, endometrial cancer, uterine cancer, salivary gland cancer, kidney cancer, vulval cancer, thyroid cancer, penis cancer, leukemia, malignant lymphoma, plasmacytoma, myeloma, or sarcoma.

2. The method of treating HER2-low expressing cancer according to claim 1 , wherein the anti-HER2 antibody comprises a heavy chain and a light chain selected from the group:

a heavy chain consisting of an amino acid sequence consisting of amino acid residues 1 to 449 of SEQ ID NO: 1 and a light chain consisting of an amino acid sequence consisting of amino acid residues 1 to 214 of SEQ ID NO: 2, and

a heavy chain consisting of the amino acid sequence of SEQ ID NO: 1 and a light chain consisting of the amino acid sequence of SEQ ID NO: 2.

3. The method of treating HER2-low expressing cancer according to claim 1 , wherein the anti-HER2 antibody comprises a heavy chain consisting of the amino acid sequence consisting of amino acid residues 1 to 449 of SEQ ID NO: 1 and a light chain consisting of the amino acid sequence consisting of amino acid residues 1 to 214 of SEQ ID NO: 2.

4. The method of treating HER2-low expressing cancer according to claim 1 , wherein the anti-HER2 antibody comprises a heavy chain consisting of the amino acid sequence of SEQ ID NO: 1 and a light chain consisting of the amino acid sequence of SEQ ID NO: 2.

5. The method of treating HER2-low expressing cancer according to claim 1 , wherein the antibody-drug conjugate has an average number of units of the drug-linker structure conjugated per antibody in a range of from 2 to 8.

6. The method of treating HER2-low expressing cancer according to claim 1 , wherein the antibody-drug conjugate has an average number of units of the drug-linker structure conjugated per antibody in a range of from 3 to 8.

7. A method of treating HER2-low expressing cancer in an individual comprising administering to an individual with HER2-low expressing cancer a pharmaceutical composition containing an antibody-drug conjugate or a salt thereof as an active component and a pharmaceutically acceptable formulation component,

wherein the antibody-drug conjugate comprises a linker and an antitumor compound represented by the following formula and anti-HER2 antibody connected to the linker:

-(Succinimid-3-yl-N)—CH 2 CH 2 CH 2 CH 2 CH 2 —C(═O)-GGFG (SEQ ID NO: 3)-NH—CH 2 —O—CH 2 —C(═O)—(NH-DX)

wherein

-(Succinimid-3-yl-N)- has a structure represented by the following formula:

which is connected to the antibody at position 3 thereof and is connected to a methylene group in the linker structure containing this structure on the nitrogen atom at position 1, and

(NH-DX) represents a group represented by the following formula:

wherein the nitrogen atom of the amino group at position 1 is the connecting position, and

wherein the HER2-low expressing cancer is lung cancer, urothelial cancer, colorectal cancer, prostate cancer, ovarian cancer, pancreatic cancer, breast cancer, bladder cancer, gastric cancer, gastrointestinal stromal tumor, uterine cervix cancer, esophageal cancer, squamous cell carcinoma, peritoneal cancer, liver cancer, hepatocellular cancer, colon cancer, rectal cancer, colorectal cancer, endometrial cancer, uterine cancer, salivary gland cancer, kidney cancer, vulval cancer, thyroid cancer, penis cancer, leukemia, malignant lymphoma, plasmacytoma, myeloma, or sarcoma.

8. The method of treating HER2-low expressing cancer according to claim 7 , wherein the anti-HER2 antibody comprises a heavy chain and a light chain selected from the group:

a heavy chain consisting of an amino acid sequence consisting of amino acid residues 1 to 449 of SEQ ID NO: 1 and a light chain consisting of an amino acid sequence consisting of amino acid residues 1 to 214 of SEQ ID NO: 2, and

a heavy chain consisting of the amino acid sequence of SEQ ID NO: 1 and a light chain consisting of the amino acid sequence of SEQ ID NO: 2.

9. The method of treating HER2-low expressing cancer according to claim 7 , wherein the anti-HER2 antibody comprises a heavy chain consisting of the amino acid sequence consisting of amino acid residues 1 to 449 of SEQ ID NO: 1 and a light chain consisting of the amino acid sequence consisting of amino acid residues 1 to 214 of SEQ ID NO: 2.

10. The method of treating HER2-low expressing cancer according to claim 7 , wherein the anti-HER2 antibody comprises a heavy chain consisting of the amino acid sequence of SEQ ID NO: 1 and a light chain consisting of the amino acid sequence of SEQ ID NO: 2.

11. The method of treating HER2-low expressing cancer according to claim 7 , wherein the antibody-drug conjugate has an average number of units of the drug-linker structure conjugated per antibody in a range of from 2 to 8.

12. The method of treating HER2-low expressing cancer according to claim 7 , wherein the antibody-drug conjugate has an average number of units of the drug-linker structure conjugated per antibody in a range of from 3 to 8.

Priority Claims (3)
JP 2014-017777 · Jan 31, 2014 · national
JP 2014-168944 · Aug 22, 2014 · national
JP 2014-227886 · Nov 10, 2014 · national
Continuity (3)
Division 15221851 · Jul 28, 2016
Continuation PCTJP2015000355 · Jan 28, 2015
Related Publication 20190077880A1 · Mar 14, 2019
Cited By (3)
US 12,186,310 US 12,319,736 US 12,698,342