To evaluate the efficacy and safety of voriconazole in Chinese patients with proven or probable deep tissue fungal infections.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
77
Pfizer Investigational Site
Guangzhou, Guangdong, China
Pfizer Investigational Site
Wuhan, Hubei, China
Pfizer Investigational Site
Wuhan, Hubei, China
Pfizer Investigational Site
Beijing, China
Percent of subjects with a Global Efficacy assessment of either "cured" or "improved" by Week 6 visit.
Safety assessment during the study period (Adverse events observed between start of treatment and follow-up visit).
Percent of subjects with a Global Efficacy assessment of either "cured" or "improved" at the time when IV administration is completed
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Pfizer Investigational Site
Beijing, China
Pfizer Investigational Site
Hangzhou, China
Pfizer Investigational Site
Shanghai, China
Pfizer Investigational Site
Shanghai, China
Pfizer Investigational Site
Tianjin, China
Pfizer Investigational Site
Tianjin, China