Micafungin: pharmacology, experimental therapeutics and clinical applications.

Article Details

Citation

Groll AH, Stergiopoulou T, Roilides E, Walsh TJ

Micafungin: pharmacology, experimental therapeutics and clinical applications.

Expert Opin Investig Drugs. 2005 Apr;14(4):489-509.

PubMed ID
15882123 [ View in PubMed
]
Abstract

Invasive fungal infections are important causes of morbidity and mortality in hospitalised patients. Current therapy with amphotericin B and antifungal triazoles has overlapping targets and is limited by toxicity and resistance. Echinocandins are a new class of antifungal drugs, which inhibit the synthesis of 1,3-beta-D-glucan. This homopolysaccharide is an important component of the cell wall of many pathogenic fungi, providing osmotic stability and functioning in cell growth and cell division. Micafungin, which is a member of the echinocandin class, exhibits in vitro fungicidal or fungistatic activity against a variety of fungal pathogens which include Candida and Aspergillus species but not Cryptococcus, Fusarium or Zygomycetes. Micafungin demonstrates linear pharmacokinetics, which are not altered by drugs metabolised through the P450 enzyme system. The preclinical and clinical data strongly support the development of micafungin for treatment of proven or suspected mucosal and invasive Candida infections in immunocompetent and immunocompromised patients. This paper reviews the preclinical and clinical pharmacology of micafungin and its potential role for treatment of fungal invasive infections in patients.

DrugBank Data that Cites this Article

Drugs
Drug Enzymes
DrugEnzymeKindOrganismPharmacological ActionActions
MicafunginArylsulfatase AProteinHumans
Unknown
Substrate
Details
MicafunginCatechol O-methyltransferaseProteinHumans
Unknown
Substrate
Details