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FLUCON®

Military Hospital of Tunis · FDA-approved active Small molecule

FLUCON® is an azole antifungal that inhibits fungal cytochrome P450-dependent lanosterol 14α-demethylase, disrupting ergosterol synthesis in the fungal cell membrane.

FLUCON® is an azole antifungal that inhibits fungal cytochrome P450-dependent lanosterol 14α-demethylase, disrupting ergosterol synthesis in the fungal cell membrane. Used for Candidiasis (oropharyngeal, esophageal, and systemic), Cryptococcal meningitis, Other fungal infections (Aspergillus, Coccidioides, and other susceptible fungi).

At a glance

Generic nameFLUCON®
Also known asFluorometholone
SponsorMilitary Hospital of Tunis
Drug classAzole antifungal
TargetFungal cytochrome P450 (lanosterol 14α-demethylase)
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved

Mechanism of action

By blocking the conversion of lanosterol to ergosterol, FLUCON® compromises the structural integrity and permeability of the fungal cell membrane, leading to cell death or growth inhibition. This mechanism is selective for fungal cells because they rely on ergosterol for membrane function, whereas mammalian cells use cholesterol instead.

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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