IP Library Granted Patent US 10,993,962
Granted Patent B2
US 10,993,962 · App. 16/274,505 · Granted May 4, 2021

Peptides and combination of peptides of non-canonical origin for use in immunotherapy against different types of cancers

Inventors: Heiko Schuster (Tuebingen, DE); Franziska Hoffgaard (Tuebingen, DE); Jens Fritsche (Dusslingen, DE); Oliver Schoor (Tuebingen, DE); Toni Weinschenk (Aichwald, DE); Daniel Johannes Kowalewski (Tuebingen, DE); Chih-Chiang Tsou (Pearland, TX)
Assignee: Immatics Biotechnologies GmbH
A61K35/17A61K38/08A61K39/001102A61K39/001114A61K39/001118A61K39/12A61K39/39A61K39/39558A61K45/06A61P35/00A61P35/02C07K7/06C07K14/4748C07K14/5434C07K16/244C07K16/2818C07K16/2821C12N5/0636A61K45/05A61K2039/5154A61K2039/5156A61K2039/5158A61K2039/55516A61K2039/55533A61K2039/55538A61K2039/55561A61K2039/572A61K2039/585
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Quick Facts
Patent No.
US 10,993,962
App. No.
16/274,505
Granted
May 4, 2021
Kind
B2
Abstract

The present invention relates to peptides, proteins, nucleic acids and cells for use in immunotherapeutic methods. In particular, the present invention relates to the immunotherapy of cancer. The present invention furthermore relates to tumor-associated T-cell peptide epitopes, alone or in combination with other tumor-associated peptides that can for example serve as active pharmaceutical ingredients of vaccine compositions that stimulate anti-tumor immune responses, or to stimulate T cells ex vivo and transfer into patients. Peptides bound to molecules of the major histocompatibility complex (MHC), or peptides as such, can also be targets of antibodies, soluble T-cell receptors, and other binding molecules.

Claims (12)

1. A peptide consisting of the amino acid sequence FASERPPSV (SEQ ID NO: 33) in the form of a pharmaceutically acceptable salt.

2. The peptide of claim 1 , wherein said peptide has the ability to bind to an WIC class-I molecule, and wherein said peptide, when bound to said WIC, is capable of being recognized by CD8 T cells.

3. The peptide of claim 1 , wherein the pharmaceutically acceptable is chloride salt or acetate salt.

4. A composition comprising the peptide of claim 1 , wherein the composition comprises an adjuvant and a pharmaceutically acceptable carrier.

5. The composition of claim 4 , wherein the peptide is in the form of a chloride or acetate salt.

6. The composition of claim 5 wherein the adjuvant is selected from the group consisting of anti-CD40 antibody, imiquimod, resiquimod, GM-CSF, cyclophosphamide, sunitinib, bevacizumab, interferon-alpha, interferon-beta, CpG oligonucleotides and derivatives, poly-(I:C) and derivatives, RNA, sildenafil, particulate formulations with poly(lactide co-glycolide) (PLG), virosomes, interleukin (IL)- 1 , IL-2, IL-4, IL-7, IL-12, IL-13, IL-15, IL-21, and IL-23.

7. The composition of claim 6 , wherein the adjuvant is IL-2.

8. A pegylated peptide consisting of the amino acid sequence of FASERPPSV (SEQ ID NO: 33) or a pharmaceutically acceptable salt thereof.

9. A composition comprising the pegylated peptide of claim 8 or pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

10. A peptide consisting of the amino acid sequence of FASERPPSV (SEQ ID NO: 33), wherein at least one amino acid of the peptide is a D-amino acid.

11. The peptide in the form of a pharmaceutically acceptable salt of claim 1 , wherein said peptide is produced by solid phase peptide synthesis or produced by a yeast cell or bacterial cell expression system.

12. A composition comprising the peptide of claim 1 , wherein the composition is a pharmaceutical composition and comprises water and a buffer.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 15, 2019
From: SCHUSTER, HEIKO; HOFFGAARD, FRANZISKA; FRITSCHE, JENS; SCHOOR, OLIVER; WEINSCHENK, TONI; KOWALEWSKI, DANIEL JOHANNES; TSOU, CHIH-CHIANG
To: IMMATICS BIOTECHNOLOGIES GMBH
Reel/Frame 048341/0140 →
Priority Claims (2)
DE 10 2018 103 944 · Feb 21, 2018 · national
DE 10 2018 107 224 · Mar 27, 2018 · national
Continuity (2)
Provisional Application 62633325 · Feb 21, 2018
Related Publication 20190255110A1 · Aug 22, 2019