IP Library Granted Patent US 12,059,464
Granted Patent B2
US 12,059,464 · App. 17/008,316 · Granted Aug 13, 2024

Combination therapy involving antibodies against Claudin 18.2 for treatment of cancer

Inventors: Ugur Sahin (Mainz, DE); Ozlem Tureci (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: Astellas Pharma Inc.; TRON—Translationale Onkologie an der Universitatsmedizin der Johannes Gutenberg-Universitat Mainz
A61K39/39558A61K31/282A61K31/337A61K31/4375A61K31/513A61K31/519A61K31/675A61K31/704A61K33/243A61K38/2013A61K45/06C07K16/30C07K16/3046C07K2317/56C07K2317/73C07K2317/732C07K2317/734
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Quick Facts
Patent No.
US 12,059,464
App. No.
17/008,316
Granted
Aug 13, 2024
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 (27)

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 stabilizing or increasing expression of CLDN18.2;

wherein the agent stabilizing or increasing expression of CLDN18.2 comprises (i) oxaliplatin and 5-fluorouracil or a prodrug thereof, (ii) epirubicin, oxaliplatin, and 5-fluorouracil or a prodrug thereof; (iii) folinic acid, oxaliplatin, and 5-fluorouracil or a prodrug thereof; (iv) irinotecan; (v) docetaxel; (vi) oxaliplatin; or (vii) a salt or ester of the agents of (i) to (vi).

2. The method of claim 1 , wherein the antibody having the ability of binding to CLDN18.2 mediates killing of cells expressing CLDN18.2 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.

3. The method of claim 1 , wherein the antibody having the ability of binding to CLDN18.2 mediates killing of cells expressing CLDN18.2 by antibody dependent cellular cytotoxicity (ADCC) mediated lysis.

4. The method of claim 1 , wherein the antibody having the ability of binding to CLDN18.2 binds to an extracellular domain of CLDN18.2.

5. The method of claim 1 , wherein the agent stabilizing or increasing expression of CLDN18.2 comprises oxaliplatin.

6. The method of claim 1 , wherein the agent stabilizing or increasing expression of CLDN18.2 comprises oxaliplatin and 5-fluorouracil or a prodrug thereof, wherein the 5-fluorouracil prodrug is capecitabine.

7. The method of claim 1 , wherein the agent stabilizing or increasing expression of CLDN18.2 comprises oxaliplatin and 5-fluorouracil.

8. The method of claim 1 , wherein the agent stabilizing or increasing expression of CLDN18.2 comprises oxaliplatin and capecitabine.

9. The method of claim 1 , wherein the agent stabilizing or increasing expression of CLDN18.2 comprises epirubicin, oxaliplatin, and 5-fluorouracil.

10. The method of claim 1 , wherein the agent stabilizing or increasing expression of CLDN18.2 comprises folinic acid, oxaliplatin, and 5-fluorouracil.

11. The method of claim 1 , wherein the agent stabilizing or increasing expression of CLDN18.2 comprises irinotecan.

12. The method of claim 1 , wherein the agent stabilizing or increasing expression of CLDN18.2 comprises docetaxel.

13. The method of claim 1 , wherein the cancer is selected from the group consisting of cancer of the esophagus, gastric cancer, cancer of the eso-gastric junction, and gastroesophageal cancer.

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

15. A method of treating gastric cancer or gastroesophageal cancer characterized by cells expressing claudin 18 splice variant 2 comprising:

administering to a patient an antibody having the ability of binding to an extracellular domain of claudin 18 splice variant 2 (CLDN18.2) in combination with an agent stabilizing or increasing expression of CLDN18.2;

wherein the antibody having the ability of binding to the extracellular domain CLDN18.2 mediates killing of cells expressing CLDN18.2 at least by antibody dependent cellular cytotoxicity (ADCC) mediated lysis; and

wherein the agent stabilizing or increasing expression of CLDN18.2 comprises (i) oxaliplatin and 5-fluorouracil or a prodrug thereof, (ii) epirubicin, oxaliplatin, and 5-fluorouracil or a prodrug thereof; (iii) folinic acid, oxaliplatin, and 5-fluorouracil or a prodrug thereof; (iv) irinotecan; (v) docetaxel; (vi) oxaliplatin; or (vii) a salt or ester of the agents of (i) to (vi).

16. The method of claim 15 , wherein the agent stabilizing or increasing expression of CLDN18.2 comprises oxaliplatin and 5-fluorouracil.

17. The method of claim 15 , wherein the agent stabilizing or increasing expression of CLDN18.2 comprises oxaliplatin and capecitabine.

18. The method of claim 15 , wherein the agent stabilizing or increasing expression of CLDN18.2 comprises epirubicin, oxaliplatin, and 5-fluorouracil.

19. The method of claim 15 , wherein the agent stabilizing or increasing expression of CLDN18.2 comprises folinic acid, oxaliplatin, and 5-fluorouracil.

20. The method of claim 15 , wherein the agent stabilizing or increasing expression of CLDN18.2 comprises oxaliplatin.

21. The method of claim 15 , wherein the agent stabilizing or increasing expression of CLDN18.2 comprises irinotecan.

22. The method of claim 15 , wherein the agent stabilizing or increasing expression of CLDN18.2 comprises docetaxel.

Assignments (5)
CORRECTIVE ASSIGNMENT TO CORRECT THE THE RECEIVING PARTY DATA PREVIOUSLY RECORDED AT REEL: 68807 FRAME: 654. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Nov 15, 2024
From: SAHIN, UGUR; TURECI, OZLEM; MITNACHT-KRAUS, RITA; JACOBS, STEFAN DENIS; UTSCH, MAGDALENA JADWIGA; HEINZ, CORNELIA ADRIANA MARIA
To: GANYMED PHARMACEUTICALS AG
Reel/Frame 069381/0193 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 29, 2024
From: STADLER, CHRISTIANE REGINA
To: TRON – TRANSLATIONALE ONKOLOGIE AN DER UNIVERSITÄTSMEDIZIN DER JOHANNES GUTENBERG-UNIVERSITÄT MAINZ GEMEINNÜTZIGE GMBH
Reel/Frame 068440/0588 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 29, 2024
From: GANYMED PHARMACEUTICALS GMBH
To: ASTELLAS PHARMA INC.
Reel/Frame 068442/0803 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 29, 2024
From: SAHIN, UGUR; TURECI, OZLEM; MITNACHT-KRAUS, RITA; JACOBS, STEFAN DENIS; UTSCH, MAGDALENA JADWIGA; HEINZ, CORNELIA ADRIANA MARIA
To: TRON – TRANSLATIONALE ONKOLOGIE AN DER UNIVERSITÄTSMEDIZIN DER JOHANNES GUTENBERG-UNIVERSITÄT MAINZ GEMEINNÜTZIGE GMBH
Reel/Frame 068807/0654 →
CHANGE OF NAME Recorded Aug 29, 2024
From: GANYMED PHARMACEUTICALS AG
To: GANYMED PHARMACEUTICALS GMBH
Reel/Frame 068807/0726 →
Priority Claims (1)
WO PCT/EP2012/002211 · May 23, 2012 · international
Continuity (4)
Continuation 15973116 · May 7, 2018
Division 15231185 · Aug 8, 2016
Continuation 14401557
Related Publication 20200390887A1 · Dec 17, 2020