IP Library Granted Patent US 9,433,675
Granted Patent B2
US 9,433,675 · App. 14/401,557 · Granted Sep 6, 2016

Combination therapy involving antibodies against claudin 18.2 for treatment of cancer

Inventors: Ugur Sahin (Mainz, DE); Özlem Türeci (Mainz, DE); Rita Mitnacht-Kraus (Friedberg, DE); Stefan Denis Jacobs (Mainz-Kastel, DE); Magdalena Jadwiga Utsch (Heidesheim am Rhein, DE); Cornelia Adriana Maria Heinz (Dalheim, DE); Christiane Regina Stadler (Bensheim, DE)
Assignees: Ganymed Pharmaceuticals AG; TRON—Translationale Onkologie an der Universitatsmedizin der Johannes Gutenberg-Universitat Mainz Gemeinnutzige GmbH
A61K39/39558A61K31/282A61K31/337A61K31/4375A61K31/513A61K31/519A61K31/675A61K31/704A61K33/24A61K38/2013A61K45/06C07K16/3046C07K2317/73C07K2317/732C07K2317/734
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,433,675
App. No.
14/401,557
Granted
Sep 6, 2016
Kind
B2
Abstract

The present invention provides a combination therapy for effectively treating and/or preventing diseases associated with cells expressing CLDN18.2, including cancer diseases such as gastric cancer, esophageal cancer, pancreatic cancer, lung cancer, ovarian cancer, colon cancer, hepatic cancer, head-neck cancer, and cancer of the gallbladder and metastases thereof.

Claims (24)

1. A method of treating a cancer characterized by cells expressing claudin 18 splice variant 2, comprising:

administering to a patient an antibody having the ability of binding to claudin 18 splice variant 2 (CLDN18.2) in combination with an agent stimulating γδ T cells and an agent stabilizing or increasing expression of CLDN18.2, wherein the agent stimulating γδ T cells is a bisphosphonate and the agent stabilizing or increasing expression of CLDN18.2 comprises at least one anthracycline, at least one platinum compound and at least one of 5-fluorouracil and prodrugs thereof.

2. The method of claim 1 , wherein the agent stabilizing or increasing expression of CLDN18.2 comprises (i) epirubicin, oxaliplatin and 5-fluorouracil, (ii) epirubicin, oxaliplatin and capecitabine, (iii) epirubicin, cisplatin and 5-fluorouracil, (iv) epirubicin, cisplatin and capecitabine, or (v) folinic acid, oxaliplatin and 5-fluorouracil.

3. The method of claim 1 , wherein the antibody having the ability of binding to CLDN18.2 binds to the first extracellular loop of CLDN18.2.

4. The method of claim 1 , wherein the antibody having the ability of binding to CLDN18.2 mediates cell killing by one or more of complement dependent cytotoxicity (CDC) mediated lysis, antibody dependent cellular cytotoxicity (ADCC) mediated lysis, induction of apoptosis and inhibition of proliferation.

5. The method of claim 1 , wherein the antibody having the ability of binding to CLDN18.2 is an antibody selected from the group consisting of (i) an antibody produced by and/or obtainable from a clone deposited under the accession no. DSM ACC2737, DSM ACC2738, DSM ACC2739, DSM ACC2740, DSM ACC2741, DSM ACC2742, DSM ACC2743, DSM ACC2745, DSM ACC2746, DSM ACC2747, DSM ACC2748, DSM ACC2808, DSM ACC2809, or DSM ACC2810, (ii) an antibody which is a chimerized or humanized form of the antibody under (i), (iii) an antibody having the specificity of the antibody under (i) and (iv) an antibody comprising the antigen binding portion or antigen binding site, in particular the variable region, of the antibody under (i) and preferably having the specificity of the antibody under (i).

6. The method of claim 1 , wherein the cancer is selected from the group consisting of cancer of the stomach, cancer of the esophagus, in particular the lower esophagus, cancer of the eso-gastric junction and gastroesophageal cancer.

7. The method of claim 1 , wherein the bisphosphonate is administered to the patient in combination with interleukin-2.

8. The method of claim 1 , wherein the γδ T cells are Vγ9Vδ2 T cells.

9. The method of claim 1 , wherein the bisphosphonate is a nitrogen-containing bisphosphonate (aminobisphosphonate).

10. The method of claim 1 , wherein the bisphosphonate is selected from the group consisting of zoledronic acid, clodronic acid, ibandronic acid, pamidronic acid, risedronic acid, minodronic acid, olpadronic acid, alendronic acid, incadronic acid, and salts thereof.

11. The method of claim 1 , wherein the bisphosphonate is zoledronic acid.

12. The method of claim 1 , wherein the at least one anthracycline is selected from the group consisting of epirubicin, doxorubicin, daunorubicin, idarubicin and valrubicin.

13. The method of claim 1 , wherein the at least one anthracycline is epirubicin.

14. The method of claim 1 , wherein the at least one platinum compound is selected from the group consisting of oxaliplatin and cisplatin.

15. The method of claim 1 , wherein the cancer is gastric cancer.

16. The method of claim 1 , wherein the cancer is metastatic gastric cancer.

17. The method of claim 1 , wherein the cancer is an esophageal adenocarcinoma, a pancreatic adenocarcinoma, or a lung adenocarcinoma.

18. The method of claim 1 , wherein the antibody has a heavy chain variable region comprising an amino acid sequence represented by SEQ ID NO: 32.

19. The method of claim 1 , wherein the antibody has a light chain variable region comprising an amino acid sequence represented by SEQ ID NO: 39.

20. The method of claim 1 , wherein the antibody has a heavy chain variable region comprising an amino acid sequence represented by SEQ ID NO: 32 and a light chain variable region comprising an amino acid sequence represented by SEQ ID NO: 39.

21. The method of claim 20 , further comprising administering interleukin-2.

22. The method of claim 20 , wherein the bisphosphonate is zoledronic acid.

23. The method of claim 20 , wherein the at least one anthracycline is epirubicin, the at least one platinum compound is oxaliplatin, and the at least one of 5-fluorouracil and prodrugs thereof is 5-fluorouracil or capecitabine.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 5, 2020
From: GANYMED PHARMACEUTICALS GMBH
To: ASTELLAS PHARMA INC
Reel/Frame 052032/0041 →
CHANGE OF NAME Recorded Mar 5, 2020
From: GANYMED PHARMACEUTICALS AG
To: GANYMED PHARMACEUTICALS GMBH
Reel/Frame 052114/0186 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 7, 2015
From: STADLER, CHRISTIANE REGINA
To: TRON- TRANSLATIONALE ONKOLOGIE AN DER UNIVERSITÄTSMEDIZIN DER JOHANNES GUTENBERG-UNIVERSITÄT MAINZ GEMEINNÜTZIGE GMBH
Reel/Frame 036748/0269 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 7, 2015
From: SAHIN, UGUR; TÜRECI, ÖZLEM; MITNACHT-KRAUS, RITA; JACOBS, STEFAN DENIS; UTSCH, MAGDALENA JADWIGA; HEINZ, CORNELIA ADRIANA MARIA
To: GANYMED PHARMACEUTICALS AG
Reel/Frame 036808/0165 →
Priority Claims (1)
EP PCT/EP2012/002211 · May 23, 2012 · regional
Continuity (1)
Related Publication 20150157711A1 · Jun 11, 2015