drugset / Trial / NCT00447902

Safety and Antiviral Activity of TPV in HCV and/or HBV HIV Coinfected Patients TDM Randomised Pilot Evaluation

NCT00447902

Phase 3 Terminated 11 enrolled Boehringer Ingelheim
Parallel-groupTreatment

Summary

The main purposes of this study are: demonstrate the safety and efficacy of TPV/r among HCV or hepatitis B virus (HBV) co-infected HIV+population, three-class (NRTI, NNRTI, and PI) experienced, with documented resistance to more than one PI. Determine pharmacokinetic data in this co-infected population and potential utility of using therapeutic drug monitoring (TDM) in improving efficacy outcomes.

Timeline

Start
2007-03
Primary completion
2008-10
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Tipranavir Small molecule
Background Ritonavir Other / unclassified