US2023190813A1PendingUtilityA1

Peptides and combination of peptides for use in immunotherapy against epithelial ovarian cancer and other cancers

Assignee: IMMATICS BIOTECHNOLOGIES GMBHPriority: Jul 15, 2015Filed: Oct 17, 2022Published: Jun 22, 2023
Est. expiryJul 15, 2035(~9 yrs left)· nominal 20-yr term from priority
G01N 33/5758C07K 14/4748A61K 2039/5158C07K 14/7051C07K 7/06A61K 39/0011C12Q 1/6886C07K 14/4727C12Q 2600/156G01N 2333/70539C07K 16/30C07K 7/08C12N 2310/16C12Q 1/6881C12Q 2600/136G01N 2500/04C12Q 2600/158G01N 33/57484C12N 15/115C12P 21/02A61K 35/17A61K 2121/00A61K 2300/00A61K 40/11A61K 40/42A61K 40/4257A61K 40/4255A61K 2239/59A61P 35/00C12N 5/0636C07K 2319/00A61P 37/04A61P 35/02C07K 16/2833C07K 16/00C07K 14/00A61K 38/00A61K 2039/505C07K 14/70539A61K 31/7088C12N 2510/00
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Claims

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

exact text as granted — not AI-modified
1 . A peptide consisting of the amino acid sequence VYFVAPAKF (SEQ ID NO: 130) in the form of a pharmaceutically acceptable salt. 
     
     
         2 . The peptide of  claim 1 , wherein said peptide has the ability to bind to an MHC class-I molecule, and wherein said peptide, when bound to said MHC, is capable of being recognized by CD8 T cells. 
     
     
         3 . The peptide of  claim 1 , wherein the pharmaceutically acceptable salt is chloride salt. 
     
     
         4 . The peptide of  claim 1 , wherein the pharmaceutically acceptable salt is acetate salt. 
     
     
         5 . A composition comprising the peptide of  claim 1 , wherein the composition comprises an adjuvant and a pharmaceutically acceptable carrier. 
     
     
         6 . The composition of  claim 5 , wherein the peptide is in the form of a chloride salt. 
     
     
         7 . The composition of  claim 5 , wherein the peptide is in the form of an acetate salt. 
     
     
         8 . 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. 
     
     
         9 . The composition of  claim 8 , wherein the adjuvant is IL-2. 
     
     
         10 . The composition of  claim 8 , wherein the adjuvant is IL-7. 
     
     
         11 . The composition of  claim 8 , wherein the adjuvant is IL-12. 
     
     
         12 . The composition of  claim 8 , wherein the adjuvant is IL-15. 
     
     
         13 . The composition of  claim 8 , wherein the adjuvant is IL-21. 
     
     
         14 . A pegylated peptide consisting of the amino acid sequence of VYFVAPAKF (SEQ ID NO: 130) or a pharmaceutically acceptable salt thereof. 
     
     
         15 . The peptide of  claim 14 , wherein the pharmaceutically acceptable salt is chloride salt. 
     
     
         16 . The peptide of  claim 14 , wherein the pharmaceutically acceptable salt is acetate salt. 
     
     
         17 . A composition comprising the pegylated peptide of  claim 14  or pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier. 
     
     
         18 . The composition of  claim 5 , wherein the pharmaceutically acceptable carrier is selected from the group consisting of saline, Ringer's solution, dextrose solution, and sustained release preparation. 
     
     
         19 . 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. 
     
     
         20 . A composition comprising the peptide of  claim 1 , wherein the composition is a pharmaceutical composition and comprises water and a buffer.

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