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 Health Network-Princess Margaret Cancer Centre, Toronto, Ontario, Canada
Massachusetts General Hospital Cancer Center, Boston, Massachusetts, United States
Universitaetsklinikum Wuerzburg, Wuerzburg, Germany
Research Site, London, United Kingdom
Pra International Group B.V, Groningen, Netherlands
St Vincent's Hospital, Darlinghurst, New South Wales, Australia
Hadassah Ein Karem Hospital; Oncology Dept, Jerusalem, Israel
Samsung Medical Center; Gastroenterology, Seoul, Korea, Republic of
FSBSI "N. N. Blokhin Russian Cancer Research Center", Moscow, Russian Federation
GSK Investigational Site, Overland Park, Kansas, United States
1320.20.1 Boehringer Ingelheim Investigational Site, Biberach, Germany
Pfizer New Haven Clinical Research Unit, New Haven, Connecticut, United States
CRU New Haven, New Haven, Connecticut, United States
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