Micafungin — Complete Research Guide (2026)
Last updated 2026-06-30
TL;DR
Micafungin (also known as Mycamine) is a peptide catalogued under Cyclic & Antimicrobial (Echinocandin). It is described as: β-1,3-glucan synthase. Documented context: Candidemia; candidose. Neutral reference entry; EU status: EU-approved prescription medicine.
What is Micafungin?
Micafungin is an echinocandin antifungal - a semisynthetic cyclic lipopeptide - administered intravenously in hospital (FDA-approved 2005 as Mycamine; also EMA-approved).
It is approved for candidaemia and invasive candidiasis, oesophageal candidiasis, and prophylaxis of Candida infections in patients undergoing haematopoietic stem-cell transplantation. Unlike caspofungin, micafungin is NOT approved for invasive aspergillosis. Its approval rests on pivotal human non-inferiority randomized controlled trials.
As a regulator-approved medicine, its efficacy and safety claims are grounded in clinical trial data rather than preclinical work.
How does Micafungin work?
Micafungin inhibits beta-(1,3)-D-glucan synthase, preventing formation of beta-1,3-glucan, an essential fungal cell-wall polysaccharide that has no human counterpart.
The resulting loss of cell-wall integrity is fungicidal against most Candida species; the fungal-specific target explains the class's generally favourable tolerability.
What does the research say about Micafungin?
- In a phase-3 double-blind trial, micafungin was non-inferior to liposomal amphotericin B for candidaemia and invasive candidiasis, with fewer treatment-related adverse events. [1]
- In a large randomized trial, micafungin was as effective as caspofungin for candidaemia and other forms of invasive candidiasis. [2]
- For antifungal prophylaxis during neutropenia after haematopoietic stem-cell transplantation, micafungin was superior to fluconazole. [3]
Clinical research & studies
The references below are the primary sources cited throughout this guide. Each links directly to PubMed or the regulator. Where evidence is preclinical (animal or in-vitro), that is stated rather than implied.
- [1] Micafungin versus liposomal amphotericin B for candidaemia and invasive candidosis: a phase III randomised double-blind trial — Kuse ER et al., Lancet 2007. (Phase-3 double-blind randomized non-inferiority trial)
- [2] Micafungin versus caspofungin for treatment of candidemia and other forms of invasive candidiasis — Pappas PG et al., Clinical Infectious Diseases 2007. (Double-blind randomized trial)
- [3] Micafungin versus fluconazole for prophylaxis against invasive fungal infections during neutropenia in patients undergoing hematopoietic stem cell transplantation — van Burik JA et al., Clinical Infectious Diseases 2004. (Randomized double-blind trial)
- [4] Micafungin: a new echinocandin — Chandrasekar PH et al., Clinical Infectious Diseases 2006. (Review)
- [5] Echinocandin antifungal drugs — Denning DW et al., Lancet 2003. (Review)
Dosing context
Micafungin is a hospital intravenous antifungal given once daily as a fixed infusion, with the dose selected by indication (treatment versus prophylaxis) and generally not requiring renal dose adjustment.
This is descriptive context only and not a dosing recommendation - antifungal selection, dose and duration are clinician decisions based on the infection, cultures and patient factors.
Side effects & safety profile
Micafungin is generally well tolerated. Key considerations are hepatic - transaminase elevations and, rarely, more serious liver injury - and infusion-related reactions, so it is given as a slow IV infusion.
It has relatively few drug interactions compared with azoles and, importantly, does not usually require dose adjustment in renal impairment. Nephrotoxicity is not a characteristic effect.
It is not approved for aspergillosis, so it should not be substituted for agents with proven mould efficacy when invasive mould infection is suspected.
Stacking & combinations
Echinocandin-based combination antifungal therapy is a specialist, clinician-directed approach for selected severe infections, not a consumer stacking practice.
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Frequently asked questions
Candidaemia and invasive candidiasis, oesophageal candidiasis, and prophylaxis of Candida infections in haematopoietic stem-cell transplant patients.
References
- [1] Micafungin versus liposomal amphotericin B for candidaemia and invasive candidosis: a phase III randomised double-blind trial — Kuse ER et al., Lancet 2007. PMID: 17482982. View sourceStudy: Phase-3 double-blind randomized non-inferiority trialMicafungin was non-inferior to liposomal amphotericin B and better tolerated for invasive candidiasis.
- [2] Micafungin versus caspofungin for treatment of candidemia and other forms of invasive candidiasis — Pappas PG et al., Clinical Infectious Diseases 2007. PMID: 17806055. View sourceStudy: Double-blind randomized trialMicafungin was as effective as caspofungin for candidaemia and invasive candidiasis.
- [3] Micafungin versus fluconazole for prophylaxis against invasive fungal infections during neutropenia in patients undergoing hematopoietic stem cell transplantation — van Burik JA et al., Clinical Infectious Diseases 2004. PMID: 15546073. View sourceStudy: Randomized double-blind trialMicafungin was superior to fluconazole for antifungal prophylaxis during post-transplant neutropenia.
- [4] Micafungin: a new echinocandin — Chandrasekar PH et al., Clinical Infectious Diseases 2006. PMID: 16575738. View sourceStudy: ReviewReviews micafungin's mechanism, spectrum, pharmacology and favourable safety profile.
- [5] Echinocandin antifungal drugs — Denning DW et al., Lancet 2003. PMID: 14550704. View sourceStudy: ReviewReviews the echinocandin class, including the beta-1,3-glucan-synthase inhibition shared by micafungin.