drugset / Trial / NCT00830804

Safety and Effectiveness of Raltegravir Plus Darunavir/Ritonavir in Treatment-Naive HIV-Infected Adults

NCT00830804

NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the effectiveness and safety of an antiretroviral therapy (ART) regimen consisting of raltegravir (RAL) and darunavir (DRV)/ritonavir (RTV) as first-line therapy in treatment-naïve participants.

Timeline

Start
2009-04
Primary completion
2010-02
Completion
2010-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Darunavir Small molecule 800 mg Oral
Subject Raltegravir Other / unclassified 400 mg Oral
Subject Ritonavir Other / unclassified 100 mg Oral