drugset / Trial / NCT00421551

Study Comparing Efficacy and Safety of Darunavir Boosted With Ritonavir to HART With 2 NRTI and Darunavir Boosted With Ritonavir in HIV-1 Infected Patients ANRS136

NCT00421551 ↗

RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate whether a monotherapy of boosted darunavir is able to maintain the virological success until 48 weeks in comparison to a standard therapy 2 INTI + darunavir/r in HIV infected patients with full viral suppression.

Timeline

Start
2007-03
Primary completion
2010-06
Completion
2011-02

Outcome

Results reported · no primary-endpoint met/missed verdict (typical of a dose-finding / safety study)

paper but discordant conclusions with respect to the noninferiority margin. PMID 20802297 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Darunavir Small molecule 600 mg —
Background Ritonavir Other / unclassified 100 mg —