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.
CRS Clinical Research Services Berlin GmbH, Berlin, Germany
California Clinical Trials Medical Group, Glendale, California, United States
Seoul National University Hospital, Seoul, Korea, Republic of
Pfizer New Haven Clinical Research Unit, New Haven, Connecticut, United States
Local Institution - 201, Milano, Italy
Local Institution - 500, Kashiwa, Japan
Local Institution - 501, Chuo-ku, Tokyo, Japan
Pfizer Clinical Research Unit, Brussels, Belgium
Washington University School of Medicine, Saint Louis, Missouri, United States
Blacktown Cancer & Haematology Centre, Blacktown, New South Wales, Australia
Centre Georges Francois Leclerc Dijon, Dijon, France
PPD Development, LP, Austin, Texas, United States
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