z-logo
open-access-imgOpen Access
Review of the pharmacology and clinical studies of micafungin
Author(s) -
Alison M. Bormann
Publication year - 2009
Publication title -
drug design development and therapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.964
H-Index - 64
ISSN - 1177-8881
DOI - 10.2147/dddt.s3242
Subject(s) - micafungin , echinocandin , tolerability , esophageal candidiasis , medicine , echinocandins , azole , pharmacology , anidulafungin , caspofungin , antifungal , aspergillosis , hematopoietic stem cell transplantation , intensive care medicine , transplantation , adverse effect , voriconazole , fluconazole , immunology , dermatology , human immunodeficiency virus (hiv) , viral disease
Micafungin, like other members of the echinocandin class, has a unique mechanism of action that inhibits the synthesis of 1,3-beta-D glucans in the fungal cell wall. It has been approved for treatment of esophageal candidiasis, invasive candidiasis including candidemia, and for prophylaxis of Candida infections in patients undergoing hematopoietic stem cell transplantation. Although efficacy and safety have also been demonstrated in pediatric populations, micafungin is approved for this indication in Europe and Japan, but not in the United States. It has demonstrated activity against Candida spp. including those that are azole-resistant as well as Aspergillus and a few other clinically important molds. It is administered intravenously as a once daily infusion and does not require dose adjustments for renal or moderate hepatic dysfunction. Its safety record, favorable tolerability profile, and few drug interactions make it an important agent for the treatment of invasive fungal infections.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom