US2021000796A1PendingUtilityA1
Formulation for use in the treatment of uremic pruritus
Assignee: DRUG DELIVERY SOLUTIONS APSPriority: Jun 17, 2016Filed: Sep 18, 2020Published: Jan 7, 2021
Est. expiryJun 17, 2036(~9.9 yrs left)· nominal 20-yr term from priority
A61P 17/04A61P 17/00A61K 31/4172A61K 31/4015A61K 9/0014A61K 47/44A61K 47/14A61K 47/26A61K 47/06A61K 9/06A61K 47/24A61K 47/32A61K 47/20A61K 45/06A61K 9/107A61K 47/186A61K 47/10A61K 47/08
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Claims
Abstract
There is provided a topical formulation comprising a nucleophile, such as amino acids and most polypetides and/or a derivative thereof, for use in the treatment or prevention of itchy dry skin caused by urea, such as in uremic pruritus, of a subject. The amino acid may be histidine and the derivative may be a histidine degradation product, a peptide of histidine, a peptide of histidine and one or more additional amino acids, and a pharmaceutically-acceptable salt of histidine.
Claims
exact text as granted — not AI-modified1 .- 15 . (canceled)
16 . A topical formulation comprising:
(a) a polyaphron composition; and (b) at least 0.2 w/w % of a nucleophilic compound.
17 . The topical formulation according to claim 16 , wherein the nucleophilic compound is a nucleophilic amino acid, a peptide and/or a derivative thereof.
18 . The topical formulation according to claim 16 , wherein the nucleophilic compound comprises a nucleophilic amino acid, and the nucleophilic amino acid comprises histidine or a derivative of histadine.
19 . The topical formulation according to claim 16 , wherein the formulation comprises:
(a) 0.5 w/w % to 5 w/w % of the nucleophilic compound.
20 . The topical formulation according to claim 16 , wherein the formulation comprises:
(a) 2 w/w % to 5 w/w % of the nucleophilic compound.
21 . The topical formulation according to claim 16 , wherein the formulation comprises:
(a) 2 w/w % to 15 w/w % of the nucleophilic compound.
22 . The topical formulation according to claim 17 , wherein the derivative is selected from one or more of a histidine degradation product, a peptide of histidine, a peptide of histidine and one or more additional amino acids, and a pharmaceutically acceptable salt of histidine.
23 . The topical formulation according to claim 18 , wherein the histidine comprises L-histidine.
24 . The topical formulation according to claim 18 , wherein the histidine and/or the derivative of histidine is the only active ingredient in the pharmaceutical composition.
25 . The topical formulation according to claim 16 , wherein the formulation further comprises pyrrolidone carboxylic acid, or one or more of the amino acids glycylglycine, cysteine, arginine, and lysine.
26 . The topical formulation according to claim 16 , wherein the pyrrolidone carboxylic acid comprises a sodium salt of the pyrrolidone carboxylic acid.
27 . The topical formulation according to claim 16 , wherein:
(a) the formulation comprises 0.5 mg/cm 2 to 2.5 mg/cm 2 skin surface, when applied to the skin, of histidine and/or a derivative of histidine.Join the waitlist — get patent alerts
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