Active Ingredient History
Miconazole is a synthetic imidazole derivative, a topical antifungal agent for use in the local treatment of vaginal, and skin and nail infections due to yeasts and dermatophytes. It is particularly active against Candida spp., Trichophyton spp., Epidermophyton spp., Microsporum spp. and Pityrosporon orbiculare (Malassezia furfur), but also possesses some activity against Gram-positive bacteria. It binds to the heme moiety of the fungal cytochrome P-450 dependent enzyme lanosterol 14-alpha-demethlyase. Inhibits 14-alpha-demethlyase, blocks formation of ergosterol and leads to the buildup of toxic methylated 14-a-sterols. Miconazole also affects the synthesis of triglycerides and fatty acids and inhibits oxidative and peroxidative enzymes, increasing the amount of active oxygen species within the cell. NCATS
Drug Pricing (per unit)
Note: This drug pricing data is preliminary, incomplete, and may contain errors.
Combination drugs
Organization | Org Type | FDA approvals | Clinical Trials involvement | Org ID | Force Sort |
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Organization | Org Type | FDA approvals | Clinical Trials involvement | Org ID | Force Sort |
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Candidiasis, Oral (approved 1973)
Candidiasis, Vulvovaginal (approved 2001)
Candidiasis (Phase 4)
Candidiasis, Oral (Phase 3)
Candidiasis, Vulvovaginal (Phase 4)
Diaper Rash (Phase 4)
Endometriosis (Phase 1)
Health (Phase 4)
Healthy Volunteers (Phase 1)
HIV (Phase 1)
HIV Infections (Phase 3)
Intertrigo (Early Phase 1)
Melanosis (Phase 4)
Mucositis (Phase 2)
Onychomycosis (Phase 2)
Otomycosis (Phase 3)
Stomatitis, Denture (Phase 3)
Tinea cruris (Phase 2)
Trichomonas Infections (Phase 2)
Trichomonas Vaginitis (Phase 2)
Vaginitis (Phase 3)
Vaginosis, Bacterial (Phase 2)
Trial | Phase | Start Date | Organizations | Indications |
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