US2010204293A1PendingUtilityA1
Pharmaceutical composition
Est. expirySep 5, 2027(~1.1 yrs left)· nominal 20-yr term from priority
A61P 31/10A61P 17/08A61K 31/4178A61K 9/0014A61P 17/00
54
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Claims
Abstract
Disclosed is an antifungal agent for external use, which is characterized by containing a compound represented by the general formula (1) below, 50-95% by mass of an alcohol, and 0.1-35% by mass of water and/or an anionic surfactant.
Claims
exact text as granted — not AI-modified1 . An antifungal agent for external use, comprising: 1) a compound represented by the general formula (1); 2) 50 to 95 mass % of an alcohol; and 3) 0.1 to 35 mass % of water and/or an anionic surfactant.
2 . The antifungal agent for external use according to claim 1 , wherein the compound represented by the general formula (1) is luliconazole.
3 . The antifungal agent for external use according to claim 1 , wherein the antifungal agent is in a form of a single-phase solution.
4 . The antifungal agent for external use according to claim 1 , comprising substantially no flammable solvent excluding an alcohol.
5 - 6 . (canceled)
7 . A method for treating mycosis comprising administering transdermally to a subject in need thereof a composition comprising: 1) a compound represented by the general formula (1); 2) 50 to 95 mass % of an alcohol; and 3) 0.1 to 35 mass % of water and/or an anionic surfactant.
8 . The method according to claim 7 , wherein the compound represented by the general formula (1) is luliconazole.
9 . The method according to claim 7 , wherein the composition is in a form of a single-phase solution.
10 . The method according to claim 7 , wherein the composition comprises substantially no flammable solvent excluding an alcohol.
11 . The method according to claim 7 , wherein the mycosis is selected from the group consisting of tinea, candidiasis, chromophytosis, and seborrheic dermatitis.
12 . The method according to claim 11 , wherein the micosis is seborrheic dermatitis.
13 . A method for stabilizing a compound represented by the general formula (1) in medicine comprising adding 1) 50 to 95 mass % of an alcohol; and 2) 0.1 to 35 mass % of water and/or an anionic surfactant to a pharmaceutical composition.
14 . The method according to claim 13 , wherein the compound represented by the general formula (1) is luliconazole.
15 . The method according to claim 13 , wherein the stabilizing effects are depletion of production of their isomers.
16 . The method according to claim 15 , wherein the isomer(s) are E form and/or Z form of luliconazole.Cited by (0)
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