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.
University of Kansas Cancer Center, Kansas City, Kansas, United States
University of Michigan Comprehensive Cancer Center, Ann Arbor, Michigan, United States
Washington University School of Medicine, Saint Louis, Missouri, United States
Celerion (Site 0001), Lincoln, Nebraska, United States
Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China
Acpru /Id# 270532, Grayslake, Illinois, United States
Dallas Clinical Research Unit, Dallas, Texas, United States
Labcorp Clinical Research Unit Inc. (Site 0001), Honolulu, Hawaii, United States
Research Site, Brooklyn, Maryland, United States
GSK Investigational Site, Cambridge, United Kingdom
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