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Voriconazole clinical practice

Instituto de Investigación Hospital Universitario La Paz · 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 nameVoriconazole clinical practice
SponsorInstituto de Investigación Hospital Universitario La Paz
Drug classTriazole antifungal
TargetFungal cytochrome P450 lanosterol 14α-demethylase (CYP51)
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved

Mechanism of action

Voriconazole is a triazole antifungal that selectively targets fungal sterol synthesis by inhibiting the enzyme lanosterol 14α-demethylase (CYP51). This leads to depletion of ergosterol, a critical component of the fungal cell membrane, causing membrane instability and fungal cell death. It has broad-spectrum activity against many clinically important fungi including Aspergillus, Candida, and Cryptococcus species.

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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