Overview
- Class of antifungal drugs that inhibit fungal cell wall synthesis
- All are semisynthetic derivatives of a fungal fermentation product (Aspergillus nidulans for anidulafungin)
- Good side-effect profile
- Potent biofilm activity
- Can only be given IV which limits their utility
Antifungal drugs in this class
- Caspofungin
- Micafungin
- Anidulafungin
- New: Rezafungin - approved by MHRA in 2024 for treatment of invasive candidiasis
Mechanism of action
Inhibit the synthesis of β-D-glucan, a major fungal cell wall component, by inhibiting the enzyme 1,3 β-D glucan synthase
- Fungicidal against Candida spp. → cause cell lysis and cell death
- Fungistatic against Aspergillus
- Some activity against Pneumocystis jirovecii – however, β-D-glucan is only found in the cyst form (not the trophic form) so cannot achieve clearance of infection
- Has been used as adjunct in case reports
Spectrum of activity
- Candida - potent against Candida spp. including in biofilm