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.
Mayo Clinic, Rochester, Minnesota, United States
UPMC Hillman Cancer Center, Pittsburgh, Pennsylvania, United States
University of Chicago, Chicago, Illinois, United States
The James Cancer Hospital and Solove Research Institute, Columbus, Ohio, United States
Shawn Aaron, The Ottawa Hospital-General Campus, Ottawa, Ontario, Canada
Felix Ratjen, The Hospital for Sick Children, Toronto, Ontario, Canada
Samsung Medical Center, Seoul, Korea, Republic of
Pfizer Investigational Site, Manchester, United Kingdom
Fred Hutchinson Cancer Research Center, Seattle, Washington, United States
University of Washington Medical Center, Seattle, Washington, United States
Jonsson Comprehensive Cancer Center, UCLA, Los Angeles, California, United States
National Institute of Allergy and Infectious Diseases (NIAID), Bethesda, Maryland, United States
UCLA Medical Center, Los Angeles, California, United States
Memorial Sloan Kettering Cancer Center, New York, New York, United States
Dana-Farber Cancer Institute, Boston, Massachusetts, United States
Ucsf Aids Crs, San Francisco, California, United States
USC CRS, Los Angeles, California, United States
Northwestern University CRS, Chicago, Illinois, United States
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