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This is an approved / prescription medicine. Do not use without a prescription and medical supervision.

EMA-approvedaka Mycamine

MicafunginComplete 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 trialKuse 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 candidiasisPappas 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 transplantationvan Burik JA et al., Clinical Infectious Diseases 2004. (Randomized double-blind trial)
  • [4] Micafungin: a new echinocandinChandrasekar PH et al., Clinical Infectious Diseases 2006. (Review)
  • [5] Echinocandin antifungal drugsDenning DW et al., Lancet 2003. (Review)

Dosing context

This is not medical advice or a usage recommendation. Dosing figures are reported research context only, cited from the published literature.

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.

Finding Micafungin vendors

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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. [1] Micafungin versus liposomal amphotericin B for candidaemia and invasive candidosis: a phase III randomised double-blind trialKuse 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. [2] Micafungin versus caspofungin for treatment of candidemia and other forms of invasive candidiasisPappas 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. [3] Micafungin versus fluconazole for prophylaxis against invasive fungal infections during neutropenia in patients undergoing hematopoietic stem cell transplantationvan 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. [4] Micafungin: a new echinocandinChandrasekar PH et al., Clinical Infectious Diseases 2006. PMID: 16575738. View sourceStudy: ReviewReviews micafungin's mechanism, spectrum, pharmacology and favourable safety profile.
  5. [5] Echinocandin antifungal drugsDenning DW et al., Lancet 2003. PMID: 14550704. View sourceStudy: ReviewReviews the echinocandin class, including the beta-1,3-glucan-synthase inhibition shared by micafungin.
This article is for educational and research purposes only. Peptides discussed here are not approved for human consumption by the FDA, EMA, or equivalent regulators outside of specific clinical contexts. Always consult a licensed medical professional before any therapeutic use.