Drug intelligence / Profile preview

azvudine + itraconazole

Development stage
Unknown
Lead developer
Genuine Biotech
Modality
Small Molecules
Administration
Oral
01

Overview

Azvudine + itraconazole is an investigational combination of two pharmaceutical agents, each with distinct mechanisms of action and indications. Azvudine is an antiviral nucleoside analog primarily developed for the treatment of HIV-1 and COVID-19. It acts as a reverse transcriptase and RNA-dependent RNA polymerase (RdRp) inhibitor, and is also being explored for antitumor activity. Itraconazole is a triazole antifungal agent used to treat various serious fungal infections by inhibiting fungal cytochrome P450-dependent lanosterol 14α-demethylase, interfering with ergosterol synthesis and cell membrane formation. The combination is being studied due to potential drug-drug interactions, as itraconazole is a potent inhibitor of the drug transporter P-glycoprotein (P-gp), and azvudine is a substrate and weak inducer of P-gp. This pairing is under evaluation to determine possible effects on azvudine’s pharmacokinetics and safety profile, especially in healthy subjects[3][5][7].

Brand names
Sporanox + none for azvudineOnmel + none for azvudine
02

Targets

Human immunodeficiency virus type 1 reverse transcriptaseABCB1 (P-glycoprotein)RdRp (Coronavirus RNA-dependent RNA polymerase)CYP51A1 (Sterol 14α-demethylase)

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