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fast itraconazole tablet

University of Maryland, Baltimore · FDA-approved active Small molecule

Itraconazole is a triazole antifungal that inhibits fungal cytochrome P450-dependent lanosterol 14α-demethylase, disrupting ergosterol synthesis in the fungal cell membrane.

Itraconazole is a triazole antifungal that inhibits fungal cytochrome P450-dependent lanosterol 14α-demethylase, disrupting ergosterol synthesis in the fungal cell membrane. Used for Fungal infections (aspergillosis, candidiasis, cryptococcosis, and other systemic mycoses).

At a glance

Generic namefast itraconazole tablet
Also known asfast dissolving itraconazole tablet
SponsorUniversity of Maryland, Baltimore
Drug classTriazole antifungal
TargetFungal cytochrome P450 lanosterol 14α-demethylase (CYP51)
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved

Mechanism of action

By blocking the conversion of lanosterol to ergosterol, itraconazole compromises the integrity and permeability of the fungal cell membrane, leading to cell death. This fast-dissolving tablet formulation is designed to improve bioavailability and onset of action compared to standard itraconazole formulations. The drug is effective against a broad spectrum of fungal pathogens 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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