IP Library › Granted Patent US 10,370,423
Granted Patent B2
US 10,370,423 · App. 15/124,640 · Granted Aug 6, 2019

Claudin-6-specific immunoreceptors and T cell epitopes

Inventors: Ugur Sahin (Mainz, DE); Özlem Türeci (Mainz, DE); Petra Simon (Mainz, DE); Tana Omokoko (Mainz, DE); Holger Hoff (Mainz, DE); Ralf-Holger Voss (Ingelheim, DE); Andrea Breitkreuz (Worms, DE); Kathleen Hobohm (Kelkheim i. Ts, DE); Karolina Anna Mroz (Wiesbaden, DE)
Assignees: Biotech Cell & Gene thrapies GMBH; Tron—Translationale Onkologie Ander Universitata tsmedizin Der Johannes Gutenberg-Universitat Main; Ganymed Pharmceuticals AG
C07K14/4748A61K39/0011C07K14/7051C07K14/70521C07K14/70539C07K16/28G01N33/505G01N33/56972G01N33/574A61K35/17A61K38/00A61K39/00A61K2039/5156A61K2039/5158C07K2317/56C07K2317/622C07K2319/02C07K2319/03C07K2319/30
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Quick Facts
Patent No.
US 10,370,423
App. No.
15/124,640
Granted
Aug 6, 2019
Kind
B2
Abstract

The present invention provides Claudin-6-specific immunoreceptors (T cell receptors and artificial T cell receptors (chimeric antigen receptors; CARs)) and T cell epitopes which are useful for immunotherapy.

Claims (8)

1. A method of treating a cancer disease comprising administering a pharmaceutical composition to a patient having claudin-6 (CLDN6)-expressing cancer cells, the pharmaceutical composition comprising a nucleic acid having a nucleic acid sequence encoding an artificial T cell receptor which specifically binds CLDN6 and comprises an amino acid sequence at least 95% identical to SEQ ID NO: 46, wherein the binding domain for CLDN6 comprises the complementarity-determining regions CDR1, CDR2, and CDR3 of the heavy chain variable region according to SEQ ID NO: 32 and the complementarity-determining regions CDR1, CDR2, and CDR3 of the light chain variable region according to SEQ ID NO: 39.

2. A method for inducing an immune response in a subject having claudin-6 (CLDN6)-expressing cancer cells, the method comprising administering to the subject a pharmaceutical composition comprising a nucleic acid having a nucleic acid sequence encoding an artificial T cell receptor which specifically binds CLDN6 and comprises an amino acid sequence at least 95% identical to SEQ ID NO: 46, wherein the binding domain for CLDN6 comprises the complementarity-determining regions CDR1, CDR2, and CDR3 of the heavy chain variable region according to SEQ ID NO: 32 and the complementarity-determining regions CDR1, CDR2, and CDR3 of the light chain variable region according to SEQ ID NO: 39.

3. A method of killing cancer cells in a subject having CLDN6-expressing cancer cells, comprising the step of providing to the subject a therapeutically effective amount of a nucleic acid having a nucleic acid sequence encoding an artificial T cell receptor which specifically binds CLDN6 and comprises an amino acid sequence at least 95% identical to SEQ ID NO: 46, wherein the binding domain for CLDN6 comprises the complementarity-determining regions CDR1, CDR2, and CDR3 of the heavy chain variable region according to SEQ ID NO: 32 and the complementarity-determining regions CDR1, CDR2, and CDR3 of the light chain variable region according to SEQ ID NO: 39.

4. A method of killing cancer cells in a subject having CLDN6-expressing cancer cells, comprising the step of providing to the subject a therapeutically effective amount of a cell comprising a nucleic acid having a nucleic acid sequence encoding an artificial T cell receptor which specifically binds CLDN6 and comprises an amino acid sequence at least 95% identical to SEQ ID NO: 46, wherein the binding domain for CLDN6 comprises the complementarity-determining regions CDR1, CDR2, and CDR3 of the heavy chain variable region according to SEQ ID NO: 32 and the complementarity-determining regions CDR1, CDR2, and CDR3 of the light chain variable region according to SEQ ID NO: 39.

5. A method of killing cancer cells in a subject having CLDN6-expressing cancer cells, comprising the step of providing to the subject a therapeutically effective amount of an immunoreactive cell obtainable from a method comprising the step of transducing a T cell with a nucleic acid having a nucleic acid sequence encoding an artificial T cell receptor which specifically binds CLDN6 and comprises an amino acid sequence at least 95% identical to SEQ ID NO: 46, wherein the binding domain for CLDN6 comprises the complementarity-determining regions CDR1, CDR2, and CDR3 of the heavy chain variable region according to SEQ ID NO: 32 and the complementarity-determining regions CDR1, CDR2, and CDR3 of the light chain variable region according to SEQ ID NO: 39.

6. A method of killing cancer cells in a subject having CLDN6-expressing cancer cells, comprising the step of providing to the subject a therapeutically effective amount of an artificial T cell receptor which specifically binds CLDN6 and comprises an amino acid sequence at least 95% identical to SEQ ID NO: 46, wherein the binding domain for CLDN6 comprises the complementarity-determining regions CDR1, CDR2, and CDR3 of the heavy chain variable region according to SEQ ID NO: 32 and the complementarity-determining regions CDR1, CDR2, and CDR3 of the light chain variable region according to SEQ ID NO: 39.

7. The method of claim 1 , 2 , 3 , 4 , 5 or 6 , wherein the artificial T cell receptor comprises a binding domain, said binding domain comprises a heavy chain variable region (VH) and a light chain variable region (VL), and wherein the VH comprises an amino acid sequence of SEQ ID NO: 32 and the VL comprises an amino acid sequence of SEQ ID NO: 39.

8. The method of claim 1 , 2 , 3 , 4 , 5 or 6 , wherein the artificial T cell receptor comprises an amino acid sequence of SEQ ID NO: 46.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 3, 2024
From: GANYMED PHARMACEUTICALS GMBH
To: ASTELLAS PHARMA INC.
Reel/Frame 066010/0062 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 17, 2017
From: SAHIN, UGUR; TÜRECI, ÖZLEM; SIMON, PETRA; OMOKOKO, TANA; HOFF, HOLGER; VOSS, RALF-HOLGER; BREITKREUZ, ANDREA; HOBOHM, KATHLEEN; MROZ, KAROLINA ANNA
To: BIONTECH CELL & GENE THERAPIES GMBH; TRON - TRANSLATIONALE ONKOLOGIE AN DER UNIVERSITÄTSMEDIZIN DER JOHANNES GUTENBERG-UNIVERSITÄT MAINZ GEMEINNÜTZIGE GMBH; UNIVERSITÄTSMEDIZIN DER JOHANNES GUTENBERG-UNIVERSITÄT MAINZ; GANYMED PHARMACEUTICALS AG
Reel/Frame 041624/0810 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 17, 2017
From: UNIVERSITÄTSMEDIZIN DER JOHANNES GUTENBERG-UNIVERSITÄT MAINZ
To: TRON - TRANSLATIONALE ONKOLOGIE AN DER UNIVERSITÄTSMEDIZIN DER JOHANNES GUTENBERG-UNIVERSITÄT MAINZ GEMEINNÜTZIGE GMBH
Reel/Frame 041624/0845 →
Priority Claims (2)
WO PCT/EP2014/000868 · Apr 1, 2014 · international
WO PCT/EP2014/072864 · Oct 24, 2014 · international
Continuity (1)
Related Publication 20170015720A1 · Jan 19, 2017