One of the triazole antifungal agents that inhibits cytochrome P-450-dependent enzymes resulting in impairment of ergosterol synthesis. It has been used against histoplasmosis, blastomycosis, cryptococcal meningitis & aspergillosis.
For the treatment of the following fungal infections in immunocompromised and non-immunocompromised patients: pulmonary and extrapulmonary blastomycosis, histoplasmosis, aspergillosis, and onychomycosis.
SGS, Paris, France
Research site, Herlev, Denmark
Research Site, Sutton, United Kingdom
1220.61.1 Boehringer Ingelheim Investigational Site, Ingelheim, Germany
University of California, San Francisco, San Francisco, California, United States
National Institute of Oncology, Budapest, Hungary
PRA Hungary Ltd., Phase I. Clinical Pharmacology Unit, Budapest, Hungary
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