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.
Stanford University School of Medicine, Stanford, California, United States
Seoul National University Hospital, Seoul, Chongno-gu, Korea, Republic of
Ajou University Medical Center, Suwon, Korea, Republic of
Ewha Womans University Mokdong Hospital, Seoul, Korea, Republic of
Samsung Medical Center, Seoul, Korea, Republic of
Postgraduate Institute of Medical Education and Research, Chandigarh, UT, India
Soonchunhyang University Bucheon Hospital, Bucheon, Kyounggi-do, Korea, Republic of
Inha University Hospital, Incheon, Korea, Republic of
Chonnam National University Hwasun Hospital, Hwasun, Jeollanam-do, Korea, Republic of
PGIMER, Chandigarh, Punjab, India
The First Hospital of Zhejiang Medical Colleage Zhejiang University, Hangzhou, Zhejiang, China
Guangzhou General Hospital of Guangzhou Military Command, Guangzhou, Guangdong, China
Stanford University School of Medicine, Stanford, California, United States
Stay informed with timely notifications on clinical trials, regulatory changes, and research advancements related to this medication.