drugset / Trial / NCT03672292

Evaluate Safety and Efficacy of the Coadministration of Ibrexafungerp With Voriconazole in Patients With Invasive Pulmonary Aspergillosis

NCT03672292

Phase 2 Terminated 22 enrolled Scynexis, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Study to evaluate the safety and efficacy of coadminstration of SCY-078 with a mold-active azole (voriconazole) compared to voriconazole in patients with invasive pulmonary aspergillosis.

Timeline

Start
2019-01-22
Primary completion
2023-03-27
Completion
2023-03-27

Drugs

EvaluationDrugModalityDoseRoute
Subject Ibrexafungerp Small molecule 500 mg Oral
Subject Voriconazole Small molecule 4 mg/kg Intravenous
Subject Voriconazole Small molecule 200 mg Intravenous