drugset / Trial / NCT00135343

A Pilot Study of Atazanavir/Ritonavir/Efavirenz as a Nucleoside Sparing Regimen

NCT00135343

Phase 3 Completed 60 enrolled Bristol-Myers Squibb
RandomizedParallel-groupOpen-label

Summary

The purpose of this study is to evaluate the safety and efficacy of a novel nucleoside sparing regimen containing atazanavir, ritonavir and efavirenz, using two different doses of atazanavir.

Timeline

Start
2004-04
Primary completion
2005-10
Completion
2005-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Atazanvir Unknown 300 mg Oral
Subject Atazanvir Unknown 400 mg Oral
Background Efavirenz Other / unclassified 600 mg Oral
Background Ritonavir Other / unclassified 100 mg Oral