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Fluconazole capsule

Jiangsu HengRui Medicine Co., Ltd. · Phase 3 active Small molecule

Fluconazole inhibits fungal cytochrome P450-dependent lanosterol 14α-demethylase, disrupting ergosterol synthesis in the fungal cell membrane.

Fluconazole inhibits fungal cytochrome P450-dependent lanosterol 14α-demethylase, disrupting ergosterol synthesis in the fungal cell membrane. Used for Candidiasis (oropharyngeal, esophageal, vaginal, and systemic), Cryptococcal meningitis, Fungal prophylaxis in immunocompromised patients.

At a glance

Generic nameFluconazole capsule
SponsorJiangsu HengRui Medicine Co., Ltd.
Drug classTriazole antifungal
TargetFungal cytochrome P450 (lanosterol 14α-demethylase)
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhasePhase 3

Mechanism of action

Fluconazole is a triazole antifungal that selectively binds to fungal cytochrome P450 enzymes, blocking the conversion of lanosterol to ergosterol, a critical component of the fungal cell membrane. This disruption leads to increased membrane permeability and cell death. The drug has broad-spectrum activity against many Candida species, Cryptococcus, and other fungi.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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