US2022362204A1PendingUtilityA1
Method for long-term treatment of rosacea
Est. expiryFeb 19, 2039(~12.6 yrs left)· nominal 20-yr term from priority
A61K 9/06A61K 31/327A61K 9/50A61K 8/38A61K 9/107A61P 17/10A61K 9/10A61P 17/00A61K 9/0014A61Q 19/00
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Claims
Abstract
A regimen for the long-term therapeutic treatment of rosacea. The regimen includes topically applying to the skin of a subject in need of said treatment a pharmaceutical composition. The pharmaceutical composition includes about 1% w/w to about 10% w/w benzoyl peroxide as an active ingredient, and a pharmaceutically acceptable carrier or excipient. The benzoyl peroxide is the only active ingredient in said pharmaceutical composition, and the pharmaceutical composition is applied once daily for a period of up to about 40 weeks to about 52 weeks, to achieve, in a group of such subjects, a success rate of about 75% to about 85%.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A regimen for the long-term therapeutic treatment of rosacea, the regimen comprising topically applying to the skin of a subject in need of said treatment a pharmaceutical composition, the pharmaceutical composition comprising about 1% w/w to about 10% w/w benzoyl peroxide as an active ingredient, and a pharmaceutically acceptable carrier or excipient, wherein the benzoyl peroxide is the only active ingredient in said pharmaceutical composition, wherein said pharmaceutical composition is applied once daily for a period of up to about 52 weeks, to achieve, in a group of such subjects, a success rate of about 75%, wherein the success rate is defined as a percentage of the number of subjects achieving clear or almost clear skin on the investor global assessment (IGA) scale after treatment with the pharmaceutical composition.
2 . The regimen of claim 1 , wherein the benzoyl peroxide is the sole active ingredient administered to the subject during the duration of the regimen.
3 . The regimen of claim 1 , wherein the pharmaceutical composition comprises about 2.5% w/w to about 10% w/w of benzoyl peroxide.
4 . The regimen of claim 3 , wherein the pharmaceutical composition comprises about 5% w/w of benzoyl peroxide.
5 . The regimen of claim 1 , wherein the benzoyl peroxide is selected from a solid, solution or suspension form.
6 . The regimen of claim 1 , wherein the regimen is a first line therapy for the treatment of rosacea.
7 . The regimen of claim 1 , wherein the rosacea is any of erythematotelengietatic rosacea, papulopustular rosacea, phymatous rosacea or ocular rosacea.
8 . The regimen of claim 1 , wherein said pharmaceutical composition is a cream or an emulsion.
9 . The regimen of claim 1 , wherein said pharmaceutical composition is an extended release formulation.
10 . The regimen of claim 9 , wherein the extended-release effect is obtained by encapsulation, microencapsulation, microspheres or coating.
11 . The regimen of claim 10 , wherein the benzoyl peroxide is encapsulated or microencapsulated.
12 . The regimen of claim 10 , wherein the benzoyl peroxide is included in a microsphere or a coating.
13 . The regimen of claim 1 , wherein the rosacea is moderate to severe rosacea.
14 . The regimen of claim 1 , wherein a percentage of subjects having no adverse effects after treatment with the pharmaceutical composition after about 52 weeks is at least 75%.
15 . The regimen of claim 14 , where the percentage of subjects having no adverse effects after treatment with the pharmaceutical composition after about 52 weeks is from about 75% to about 85%.
16 . The regimen of claim 1 , wherein the adverse effect is selected from itching, burning, dryness, itching and a combination thereof.Cited by (0)
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