Drug intelligence / Profile preview

azole + anidulafungin

Development stage
Unknown
Lead developer
Erasmus MC
Modality
Peptides, Small Molecules
Administration
Intravenous, Oral
01

Overview

azole + anidulafungin is a combination antifungal regimen being investigated by Erasmus Medical Center for the treatment of invasive aspergillosis (IA). This combination therapy pairs a triazole antifungal—typically voriconazole, isavuconazole, or posaconazole—with anidulafungin, an echinocandin. The mechanism of action involves a dual-target approach to fungal cell integrity: the azole component inhibits the enzyme lanosterol 14-alpha-demethylase (CYP51), which is essential for the synthesis of ergosterol in the fungal cell membrane, while anidulafungin inhibits 1,3-beta-D-glucan synthase, preventing the synthesis of 1,3-beta-D-glucan, a critical structural component of the fungal cell wall. This combination is being evaluated in a Phase 3 pragmatic superiority trial to determine if initial combination therapy can decrease overall mortality compared to triazole monotherapy in immunocompromised and ICU patients with invasive aspergillosis.

Other names
Azole-echinocandin combination therapyAzole-anidulafungin combination
02

Targets

FKS (1,3-beta-D-glucan synthase component FKS1)CYP51A1 (Sterol 14α-demethylase)

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