drugset / Trial / NCT00159822

Voriconazole For Chronic Bronchopulmonary Aspergillosis

NCT00159822

Phase 2/3 Completed 48 enrolled Pfizer
Non-randomizedSingle-groupOpen-labelTreatment

Summary

To evaluate the efficacy of voriconazole (VFend(R)) as first line treatment for proven chronic bronchopulmonary aspergillosis, in minimally immunocompromised or non-immunocompromised patients after 6 months of treatment i.e. chronic necrotizing pulmonary

Timeline

Start
2005-07
Primary completion
2008-12
Completion
2008-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Voriconazole Small molecule 4 mg/kg Oral
Subject Voriconazole Small molecule 200 mg Oral

Indications