US2014329758A1PendingUtilityA1

Peptide inhibitors for mediating stress responses

Assignee: YEDA RES & DEVPriority: Aug 23, 2004Filed: Jul 27, 2014Published: Nov 6, 2014
Est. expiryAug 23, 2024(expired)· nominal 20-yr term from priority
A61P 43/00A61P 37/00A61P 7/04A61P 5/16A61P 37/06A61P 39/00A61P 9/10A61P 3/10A61P 7/06A61P 27/06A61P 27/02A61P 25/00A61P 31/04A61P 25/08A61P 25/16A61P 25/28A61P 35/00A61P 29/00A61P 17/06A61P 17/00A61P 15/08A61P 19/04A61P 11/16A61P 1/16A61P 11/00A61P 21/04A61P 19/10A61P 19/02A61P 1/00A61P 19/00A61P 1/04A61P 13/12A61P 17/16C07K 7/08A61K 39/0008A61K 39/0005A61K 38/00C07K 7/06C07K 14/435
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Claims

Abstract

The present invention relates to peptides capable of inhibiting cellular and immune stress responses in a eukaryotic cell. The invention provides compositions and methods for the treatment of human degenerative diseases and inflammation, utilizing these peptides.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method for treating a condition selected from the group consisting of Parkinson's disease, multiple sclerosis, stroke and myocardial infarction in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a peptide comprising an epitope immunoreactive with an anti-idiotypic antibody directed against an anti-p53 antibody, wherein the anti-p53 antibody is immunoreactive with at least a part of the regulatory domain of the C-terminus of p53, and wherein the peptide exhibits at least one activity selected from anti-apoptotic activity and anti-inflammatory activity wherein the length of the peptide is 7 to 25 amino acids and has the amino acid sequence as set forth in SEQ ID NO: 1. 
     
     
         2 . The method of  claim 1 , wherein the anti-p53 antibody is PAb-421. 
     
     
         3 . The method of  claim 1 , wherein the amino acid sequence of said peptide is as set forth in SEQ ID NO: 1. 
     
     
         4 . The method of  claim 1 , wherein the peptide is administered to the subject by a route selected from oral, topical, transdermal and parenteral. 
     
     
         5 . The method of  claim 1 , wherein said condition is Parkinson's disease. 
     
     
         6 . The method of  claim 1 , wherein said condition is multiple sclerosis. 
     
     
         7 . The method of  claim 1 , wherein said condition is myocardial infarction. 
     
     
         8 . The method of  claim 1 , wherein said condition is stroke.

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