Drug intelligence / Profile preview

liposomal amphotericin B + posaconazole + isavuconazole

Development stage
Unknown
Lead developer
Institute of Hematology and Blood Diseases Hospital
Modality
Lipid-based Nanoparticles → Nanoparticles → Drug Delivery Systems, Small Molecules
Administration
Intravenous, Oral
01

Overview

This combination therapy involves the co-administration of liposomal amphotericin B (L-AmB) with the triazole antifungals posaconazole and/or isavuconazole. Liposomal amphotericin B is a polyene antifungal that acts by binding to ergosterol in fungal cell membranes, creating pores that lead to cell death; the liposomal formulation is designed to reduce systemic toxicity, particularly nephrotoxicity. Posaconazole and isavuconazole are second-generation triazoles that inhibit the enzyme lanosterol 14α-demethylase (CYP51), thereby blocking the biosynthesis of ergosterol, an essential component of the fungal cell membrane. This multi-drug regimen is being evaluated by the Institute of Hematology & Blood Diseases Hospital in China for the treatment of mucormycosis in adult patients with hematologic malignancies. The strategy aims to improve clinical outcomes in this high-risk population by leveraging potential synergistic antifungal activity and providing a transition path from intravenous to oral therapy.

Other names
L-AmB + posaconazole + isavuconazole
02

Targets

CYP51A1 (Sterol 14α-demethylase)Ergosterol

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