Last reviewed · How we verify

Vfend (voriconazole) tablet

Seoul National University Hospital · FDA-approved active Small molecule

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

Voriconazole inhibits fungal cytochrome P450-dependent lanosterol 14α-demethylase, disrupting ergosterol synthesis in the fungal cell membrane. Used for Invasive aspergillosis, Esophageal candidiasis, Candidemia in non-neutropenic patients.

At a glance

Generic nameVfend (voriconazole) tablet
Also known asOral
SponsorSeoul National University Hospital
Drug classTriazole antifungal
TargetCytochrome P450 14α-demethylase (CYP51)
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved

Mechanism of action

By blocking a key enzyme in the ergosterol biosynthesis pathway, voriconazole causes depletion of ergosterol and accumulation of toxic sterol precursors, leading to fungal cell membrane instability and cell death. This mechanism is selective for fungi because the target enzyme and ergosterol-dependent membrane structure are unique to fungal cells, making it effective against a broad spectrum of fungal pathogens.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

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

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: