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anidulafungin and voriconazole

Pfizer · FDA-approved active Small molecule

Anidulafungin inhibits fungal cell wall synthesis by targeting β-1,3-glucan synthase, while voriconazole inhibits fungal cytochrome P450-dependent sterol synthesis, together providing broad-spectrum antifungal coverage.

Anidulafungin inhibits fungal cell wall synthesis by targeting β-1,3-glucan synthase, while voriconazole inhibits fungal cytochrome P450-dependent sterol synthesis, together providing broad-spectrum antifungal coverage. Used for Invasive candidiasis, Invasive aspergillosis, Other serious fungal infections in immunocompromised patients.

At a glance

Generic nameanidulafungin and voriconazole
SponsorPfizer
Drug classEchinocandin and triazole antifungal combination
Targetβ-1,3-glucan synthase (anidulafungin); fungal CYP51/lanosterol 14α-demethylase (voriconazole)
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved

Mechanism of action

Anidulafungin is an echinocandin that disrupts the structural integrity of the fungal cell wall by inhibiting β-1,3-glucan synthase, leading to cell lysis and death. Voriconazole is a triazole that blocks ergosterol synthesis by inhibiting fungal CYP51, disrupting cell membrane function. This combination targets two distinct mechanisms of fungal cell integrity, providing synergistic activity against a wide range of fungal pathogens.

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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