US2011190214A1PendingUtilityA1
Advantageous Salts of Mu-Opiate Receptor Peptides
Individually held — no corporate assignee on recordPriority: Dec 13, 2007Filed: Dec 15, 2008Published: Aug 4, 2011
Est. expiryDec 13, 2027(~1.4 yrs left)· nominal 20-yr term from priority
Inventors:Theodore E. Maione
A61P 25/36A61P 29/00A61P 25/30A61P 25/04A61P 1/00A61P 1/04A61K 38/00C07K 5/1016C07K 5/10
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Claims
Abstract
The subject invention provides advantageous new salts of mu-opiate receptor peptides. These salts have been found to have excellent properties in terms of their crystal structure, stability, solubility, lack of impurities and/or the ability to be produced, with these advantageous properties, in amounts sufficient for the production of therapeutic compositions.
Claims
exact text as granted — not AI-modified1 . A peptide salt wherein the peptide has a sequence selected from SEQ ID NOs: 1-26 and the salt is selected from the group consisting of maleate, hydrochloride, lactate and aspartate.
2 . The peptide salt, according to claim 1 , wherein the peptide is SEQ ID NO:13.
3 . The peptide salt, according to claim 2 , wherein the salt is the hydrochloride salt.
4 . A pharmaceutical composition comprising a peptide salt wherein the peptide has a sequence selected from SEQ ID NOs: 1-16 and the salt is selected from the group consisting of maleate, hydrochloride, lactate and aspartate.
5 . The pharmaceutical composition, according to claim 4 , wherein the peptide is SEQ ID NO:13.
6 . The pharmaceutical composition, according to claim 5 , wherein the salt is the hydrochloride salt.
7 . A method for treating a condition that is modulated by μ-opiate receptor activity, wherein said method comprises administering, to a patient in need of such treatment a peptide salt wherein the peptide has a sequence selected from SEQ ID NOs: 1-26 and the salt is selected from the group consisting of maleate, hydrochloride, lactate and aspartate.
8 . The method, according to claim 7 , wherein the peptide is SEQ ID NO:13.
9 . The method, according to claim 8 , wherein the salt is the hydrochloride salt.
10 . The method, according to claim 7 , which is used to provide analgesia or to treat a condition selected from the group consisting of gastrointestinal disorders, inflammation, and drug dependence.Join the waitlist — get patent alerts
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