Drug intelligence / Profile preview

ibrexafungerp + voriconazole

Development stage
Unknown
Lead developer
Scynexis
Modality
Small Molecules
Administration
Oral
01

Overview

**ibrexafungerp + voriconazole** is an investigational combination of two antifungal drugs: ibrexafungerp, a semisynthetic triterpenoid and first-in-class oral (1→3)-β-d-glucan synthase inhibitor that disrupts fungal cell wall synthesis, and voriconazole, a triazole antifungal that inhibits the fungal cell membrane ergosterol biosynthesis by targeting lanosterol 14-alpha-demethylase. This combination is being studied for improved efficacy in treating invasive pulmonary aspergillosis (IPA) and possibly other serious fungal infections, especially in immunocompromised patients. Preclinical data suggest the combination yields additive or synergistic effects against Aspergillus species by targeting complementary pathways in fungal cell integrity. Clinical trials (e.g., SCYNERGIA, NCT03672292) are investigating its safety and efficacy.

02

Targets

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

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