IP Library › Granted Patent US 10,844,133
Granted Patent B2
US 10,844,133 · App. 15/866,139 · Granted Nov 24, 2020

Cancer therapy using CLDN6 target-directed antibodies in vivo

Inventors: Ugur Sahin (Mainz, DE); Ozlem Tureci (Mainz, DE); Michael Koslowski (Oberschleissheim, DE); Korden Walter (Wiesbaden, DE); Maria Kreuzberg (Mainz, DE); Sylvia Luxen (Mannheim, DE)
Assignees: Ganymed Pharmaceuticals GmbH; Johannes Gutenberg-Universitat Mainz
C07K16/30C07K16/28C07K16/3015C07K16/3023C07K16/3038C07K16/3046C07K16/3053C07K16/3069A61K2039/505C07K2317/24C07K2317/732C07K2317/734C07K2317/92
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Quick Facts
Patent No.
US 10,844,133
App. No.
15/866,139
Granted
Nov 24, 2020
Kind
B2
Abstract

The invention relates to the treatment and/or prevention of tumor diseases associated with cells expressing CLDN6, in particular cancer and cancer metastasis using antibodies which bind to CLDN6. The present application demonstrates that the binding of antibodies to CLDN6 on the surface of tumor cells is sufficient to inhibit growth of the tumor and to prolong survival and extend the lifespan of tumor patients. Furthermore, binding of antibodies to CLDN6 is efficient in inhibiting growth of CLDN6 positive germ cell tumors such as teratocarcinomas or embryonal carcinomas, in particular germ cell tumors of the testis.

Claims (24)

1. A bispecific antibody comprising a first antigen binding site having a binding specificity for CLDN6 and a second antigen binding site having a binding specificity for a second antigen,

wherein the first antigen binding site comprises a heavy chain CDR1 (HCDR1), a HCDR2, a HCDR3, a light chain CDR1 (LCDR1), a LCDR2, and a LCDR3 of an antibody produced by or obtainable from a hybridoma selected from the group consisting of:

a. a hybridoma deposited under accession no. DSM ACC3059 (GT512muMAB 36A),

b. a hybridoma deposited under accession no. DSM ACC3058 (GT512muMAB 27A), and

c. a hybridoma deposited under accession no. DSM ACC3057 (GT512muMAB 5F2D2).

2. The bispecific antibody of claim 1 , wherein the bispecific antibody is a single chain antibody.

3. The bispecific antibody of claim 1 , wherein the first antigen binding site is not capable of detectably binding to at least one of (i) CLDN3 associated with the surface of a cell that expresses CLDN3, (ii) CLDN4 associated with the surface of a cell that expresses CLDN4, or (iii) CLDN9 associated with the surface of a cell that expresses CLDN9.

4. The bispecific antibody of claim 1 , wherein CLDN6 has the amino acid sequence of SEQ ID NO: 2 or the amino acid sequence of SEQ ID NO: 6.

5. The bispecific antibody of claim 1 , wherein the hybridoma is the hybridoma deposited under accession no. DSM ACC3059 (GT512muMAB 36A).

6. The bispecific antibody of claim 5 , wherein the bispecific antibody is a single chain antibody.

7. The bispecific antibody of claim 5 , wherein the first antigen binding site is not capable of detectably binding to at least one of (i) CLDN3 associated with the surface of a cell that expresses CLDN3, (ii) CLDN4 associated with the surface of a cell that expresses CLDN4, or (iii) CLDN9 associated with the surface of a cell that expresses CLDN9.

8. The bispecific antibody of claim 5 , wherein CLDN6 has the amino acid sequence of SEQ ID NO: 2 or the amino acid sequence of SEQ ID NO: 6.

9. The bispecific antibody of claim 1 , wherein the hybridoma is the hybridoma deposited under accession no. DSM ACC3058 (GT512muMAB 27A).

10. The bispecific antibody of claim 9 , wherein the bispecific antibody is a single chain antibody.

11. The bispecific antibody of claim 9 , wherein the first antigen binding site is not capable of detectably binding to at least one of (i) CLDN3 associated with the surface of a cell that expresses CLDN3, (ii) CLDN4 associated with the surface of a cell that expresses CLDN4, or (iii) CLDN9 associated with the surface of a cell that expresses CLDN9.

12. The bispecific antibody of claim 9 , wherein CLDN6 has the amino acid sequence of SEQ ID NO: 2 or the amino acid sequence of SEQ ID NO: 6.

13. The bispecific antibody of claim 1 , wherein the hybridoma is the hybridoma deposited under accession no. DSM ACC3057 (GT512muMAB 5F2D2).

14. The bispecific antibody of claim 13 , wherein the bispecific antibody is a single chain antibody.

15. The bispecific antibody of claim 13 , wherein the first antigen binding site is not capable of detectably binding to at least one of (i) CLDN3 associated with the surface of a cell that expresses CLDN3, (ii) CLDN4 associated with the surface of a cell that expresses CLDN4, or (iii) CLDN9 associated with the surface of a cell that expresses CLDN9.

16. The bispecific antibody of claim 13 , wherein CLDN6 has the amino acid sequence of SEQ ID NO: 2 or the amino acid sequence of SEQ ID NO: 6.

17. A pharmaceutical composition comprising the bispecific antibody of claim 1 .

18. A pharmaceutical composition comprising the bispecific antibody of claim 5 .

19. A pharmaceutical composition comprising the bispecific antibody of claim 9 .

20. A pharmaceutical composition comprising the bispecific antibody of claim 13 .

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 15, 2019
From: GANYMED PHARMACEUTICALS AG
To: GANYMED PHARMACEUTICALS GMBH
Reel/Frame 049749/0977 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 9, 2018
From: SAHIN, UGUR; TURECI, OZLEM; KOSLOWSKI, MICHAEL; WALTER, KORDEN; KREUZBERG, MARIA; LUXEN, SYLVIA
To: GANYMED PHARMACEUTICALS AG; JOHANNES GUTENBERG-UNIVERSITAT MAINZ
Reel/Frame 044577/0166 →
Priority Claims (1)
EP 10006957 · Jul 6, 2010 · regional
Continuity (4)
Continuation 15206039 · Jul 8, 2016
Division 13808423
Provisional Application 61361632 · Jul 6, 2010
Related Publication 20180142033A1 · May 24, 2018