Isavuconazole: Mechanism of Action, Clinical Efficacy, and Resistance
- PMID: 33260353
- PMCID: PMC7712939
- DOI: 10.3390/jof6040324
Isavuconazole: Mechanism of Action, Clinical Efficacy, and Resistance
Erratum in
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Correction: Ellsworth, M.; Ostrosky-Zeichner, L. Isavuconazole: Mechanism of Action, Clinical Efficacy, and Resistance. J. Fungi 2020, 6, 324.J Fungi (Basel). 2025 Mar 17;11(3):226. doi: 10.3390/jof11030226. J Fungi (Basel). 2025. PMID: 40105014 Free PMC article.
Abstract
Increasing incidence of invasive fungal infections combined with a growing population of immunocompromised hosts has created a rising need for antifungal agents. Isavuconazole, a second-generation broad-spectrum triazole with activity against yeasts, dimorphic fungi, and molds, has a favorable safety profile and predictable pharmacokinetics. Patients typically tolerate isavuconazole well with fewer drug-drug interactions. Clinical trials have found it to be noninferior to voriconazole for invasive aspergillosis, an alternative therapy for salvage treatment of mucormycosis, and suitable for stepdown therapy with invasive candidiasis. Cross-resistance with other triazoles is common. More studies are needed to determine the role of isavuconazole in anti-mold prophylaxis in high-risk patients.
Keywords: Aspergillus; Candida; Mucorales; invasive fungal disease; isavuconazole; triazole.
Conflict of interest statement
L.O. received speaking, consulting, and/or research funds from Astellas, Pfizer, Cidara, Amplyx, Scynexis, Mayne, F2G, Viracor, and Gilead. M.E. has no reported conflicts.
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