drugset / Trial / NCT00034671

PK/PD Study of Posaconazole for Empiric Treatment of Invasive Fungal Infections in Neutropenic Patients or Treatment of Refractory Invasive Fungal Infections (Study P01893)

NCT00034671

Phase 2 Completed 98 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupOpen-labelTreatment

Summary

This phase II study will be conducted to: 1. evaluate the pharmacokinetics, safety, tolerance, and efficacy of different dosing schedules of Posaconazole in immunocompromised hosts with a variety of refractory invasive fungal infections or in subjects who require empiric antifungal therapy and 2. identify the dosing schedule that provides the most consistent therapeutic drug exposure in this patient population.

Timeline

Start
2001-01
Primary completion
2001-11
Completion
2002-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Posaconazole Small molecule 400 mg Oral
Subject Posaconazole Small molecule 600 mg Oral
Subject Posaconazole Small molecule 800 mg Oral