US2011150890A1PendingUtilityA1
Use of cgrp antagonist compounds for treatment of psoriasis
Est. expiryAug 12, 2022(expired)· nominal 20-yr term from priority
Inventors:Birkir Sveinsson
A61K 38/482A61K 31/727G01N 33/5044A61K 38/225A61K 31/166A61K 31/517A61P 17/06G01N 33/502G01N 33/566A61P 17/00G01N 33/5088G01N 33/74G01N 2333/5753A61K 31/00C07K 16/26G01N 33/5008A61K 31/506A61K 31/4184A61K 38/23A61K 9/107A61K 47/44A61P 17/02A61K 9/0014
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Claims
Abstract
The invention provides methods and compositions for treating, preventing and/or remedying psoriasis, based on compounds that have a calcitonin-related gene peptide (CGRP) antagonistic effect. Methods are also disclosed for identifying compounds with CGRP antagonist activity which thereby are suitable candidate compounds for treating psoriasis.
Claims
exact text as granted — not AI-modified1 . A method of treating or remedying psoriasis in a subject in need thereof, comprising administering to the subject a therapeutically effective dose of at least one calcitonin gene-related peptide CGRP antagonist compound in a pharmaceutical acceptable formulation.
2 . The method according to claim 1 , wherein the at least one CGRP antagonist compound is selected from the group consisting of 4-sulfinyl benzamide compounds, 3,4-dinitrobenzamide compounds, benzamidazolinyl piperadine compounds, anti-CGRP antibodies, a peptide comprising SEQ ID NO:1, tryptase active polypeptide, BIBN4096BS, and heparin.
3 . The method according to claim 1 , wherein the at least one CGRP antagonist compound is administered locally.
4 . (canceled)
5 . The method according to claim 1 , wherein the CGRP antagonist compound is administered topically.
6 - 14 . (canceled)
15 . The method according to claim 1 , wherein the at least one CGRP antagonist is administered topically, dermally, intradermally, subcutaneously, via dermal infusion, or via subcutaneous infusion.
16 . The method according to claim 1 , wherein said at least one CGRP antagonist compound comprises a polypeptide of SEQ ID NO:1.
17 . The method according to claim 1 , wherein said at least one CGRP antagonist compound consists essentially of a polypeptide of SEQ ID NO:1.
18 . The method according to claim 1 , wherein the at least one CGRP antagonist compound is a CGRP peptide which lacks wild type CGRP activity and binds to CGRP receptor.
19 . The method according to claim 1 , wherein the at least one CGRP antagonist is administered dermally, intradermally, subcutaneously, via dermal infusion, via subcutaneous infusion, or via microdialysis.
20 . The method according to claim 1 , wherein the at least one CGRP antagonist compound is BIBN4096BS.
21 . The method according to claim 1 , wherein the pharmaceutically acceptable formulation consists essentially of a CGRP antagonist and an excipient.
22 . The method according to claim 1 , further comprising exposing the subject to UVB radiation and/or administering a cell division inhibitor to the subject.Join the waitlist — get patent alerts
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