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.
Dr. Vince Clinical Research, Overland Park, Kansas, United States
Research Site, Berlin, Germany
Khyber Teaching Hospital, Peshawar, KPK, Pakistan
Celerion, Tempe, Arizona, United States
Fortrea Clinical Research Unit Inc, Madison, Wisconsin, United States
ICON, Groningen, Netherlands
ICON, plc, San Antonio, Texas, United States
Research Site, Brooklyn, Maryland, United States
Scientia Clinical Research, Sydney, Randwick NSW, Australia
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
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