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.
Research Site, Nottingham, United Kingdom
Taisho Pharmaceutical Co., Ltd selected site, Tokyo, Japan
WCCT, Cypress, California, United States
Onkologikoa, Donostia, Gipuzkoa, Spain
California Cancer Associates for Research and Excellence, Inc. (cCARE), Encinitas, California, United States
Northwestern University-Robert H. Lurie Comprehensive Cancer Center, Chicago, Illinois, United States
National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital & Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen, Guangdong, China
Local Institution, Salt Lake City, Utah, United States
QPS Bio-kinetic, Springfield, Missouri, United States
Celerion, Tempe, Arizona, United States
US1517, Miami, Florida, United States
Covance Clinical Research Unit, Dallas, Texas, United States
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