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slow itraconazole tablet

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

Slow itraconazole tablet is a modified-release formulation of itraconazole that inhibits fungal cytochrome P450-dependent lanosterol 14α-demethylase, disrupting ergosterol synthesis in fungal cell membranes.

Slow itraconazole tablet is a modified-release formulation of itraconazole that inhibits fungal cytochrome P450-dependent lanosterol 14α-demethylase, disrupting ergosterol synthesis in fungal cell membranes. Used for Fungal infections (broad-spectrum including aspergillosis, candidiasis, and other systemic mycoses).

At a glance

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

Mechanism of action

Itraconazole is a triazole antifungal that selectively targets fungal sterol synthesis by inhibiting the demethylation of lanosterol to ergosterol. The slow/modified-release formulation extends drug exposure and improves bioavailability compared to standard itraconazole formulations, allowing for more consistent antifungal activity. This mechanism is effective against a broad spectrum of fungi including Aspergillus, Candida, and other clinically important 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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