IP Library Granted Patent US 8,895,514
Granted Patent B2
US 8,895,514 · App. 13/841,013 · Granted Nov 25, 2014

Composition of tumor-associated peptides and related anti-cancer vaccine for the treatment of glioblastoma (GBM) and other cancers

Inventors: Toni Weinschenk (Aichwald, DE); Oliver Schoor (Tuebingen, DE); Claudia Trautwein (Wuelfrath, DE); Norbert Hilf (Kirchentellinsfurt, DE); Steffan Walter (Reutlingen, DE); Harpreet Singh (Tuebingen, DE)
Assignee: Immatics Biotechnologies GmbH
A61K39/0011C07K7/06C07K7/08A61K2039/5154A61K2039/53
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Quick Facts
Patent No.
US 8,895,514
App. No.
13/841,013
Granted
Nov 25, 2014
Kind
B2
Abstract

The present invention relates to immunotherapeutic peptides and their use in immunotherapy, in particular the immunotherapy of cancer. The present invention discloses tumor-associated T-helper cell peptide epitopes, alone or in combination with other tumor-associated peptides that serve as active pharmaceutical ingredients of vaccine compositions which stimulate anti-tumor immune responses. In particular, the composition of the peptides of the present invention can be used in vaccine compositions for eliciting anti-tumor immune responses against gliomas.

Claims (22)

1. A pharmaceutical composition, comprising: (i) at least two immunogenic peptides from 8 to 100 amino acids in length, one of said peptides comprising an amino acid sequence that is at least 80% identical to SEQ ID NO: 7 and (ii) a pharmaceutically acceptable carrier.

2. The pharmaceutical composition according to claim 1 , wherein another of said peptides comprises an amino acid sequence that is at least 80% identical to a sequence selected from the group consisting of SEQ ID NO: 9 to SEQ ID NO: 20.

3. The pharmaceutical composition according to claim 2 , wherein the second peptide is selected from the group consisting of SEQ ID NO: 1 to SEQ ID NO: 20.

4. The pharmaceutical composition according to claim 1 , wherein at least one of the at least two peptides includes non-peptide bonds.

5. The pharmaceutical composition of claim 1 , where the first peptide comprises SEQ ID NO: 7.

6. The pharmaceutical composition of claim 1 , wherein the first peptide consists of a core sequence consisting of SEQ ID NO: 7 with extensions of 1 to 10 amino acids on the C-terminal and/or the N-terminal of the core sequence.

7. The pharmaceutical composition of claim 1 , wherein the first peptide consists of SEQ ID NO: 7.

8. The pharmaceutical composition according to claim 1 , further comprising at least one suitable adjuvant.

9. The pharmaceutical composition according to claim 8 , wherein the adjuvant is selected from the group consisting of colony-stimulating factors, GM-CSF, imiquimod, and resiquimod.

10. The pharmaceutical composition according to claim 8 , comprising two to four adjuvants.

11. The pharmaceutical composition according to claim 10 , wherein least two of the adjuvants are selected from the group consisting of CP-870,893, CpG7909, GM-CSF, imiquimod, and resiquimod.

12. The pharmaceutical composition according to claim 1 , additionally comprising at least one antigen presenting cell.

13. The pharmaceutical composition according to claim 12 , wherein the antigen presenting cell is a dendritic cell.

14. The pharmaceutical composition according to claim 12 , wherein the at least one antigen presenting cell:

a) is pulsed or loaded with the peptide; or

b) comprises an expression construct encoding the peptide.

15. The pharmaceutical composition of claim 1 , wherein the composition is administered intravenously, intra-arterially, intra-peritoneally, intramuscularly, intradermally, intratumorally, orally, dermally, nasally, buccally, rectally, vaginally, by inhalation, or by topical administration.

16. A method for treating and/or preventing a cancer in a patient, the method comprising administering to the patient a therapeutically effective amount of the pharmaceutical composition of claim 1 .

17. The method according to claim 16 , wherein the pharmaceutical composition is an anti-cancer vaccine.

18. The method of claim 17 , wherein the cancer is one or more of cancer of the buccal cavity or pharynx, cancer of the digestive tract, cancer of the colon, rectum, or anus, cancer of the respiratory tract, breast cancer, cancer of the cervix uteri, vagina, or vulva, cancer of the uterine corpus or ovary, cancer of the male genital tract, cancer of the urinary tract, bone or soft tissue cancer, Kaposi sarcoma, melanoma of the skin, ocular melanoma, non-melanoma eye cancer, cancer of the brain and central nervous system, cancer of the thyroid and other endocrine glands, Hodgkin Lymphoma, Non-Hodgkin Lymphoma, myeloma, renal cancer, colorectal cancer, lung cancer, breast cancer, pancreatic cancer, prostate cancer, gastric cancer, GIST or glioblastoma.

19. The method according to claim 18 , wherein the cancer is colorectal cancer.

20. The method according to claim 18 , wherein the cancer is glioblastoma.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 27, 2013
From: WEINSCHENK, TONI; SCHOOR, OLIVER; TRAUTWEIN, CLAUDIA; HILF, NORBERT; WALTER, STEFFAN; SINGH, HARPREET
To: IMMATICS BIOTECHNOLOGIES GMBH
Reel/Frame 030093/0466 →
Priority Claims (1)
EP 08017305 · Oct 1, 2008 · regional
Continuity (5)
Division 13588206 · Aug 17, 2012
Division 12571602 · Oct 1, 2009
Continuation PCTEP2009006979 · Sep 28, 2009
Provisional Application 61105970 · Oct 16, 2008
Related Publication 20130309193A1 · Nov 21, 2013