drugset / Trial / NCT00135395

A Phase IIIb Study Comparing Two Boosted Protease Inhibitor-based HAART Regimens in HIV-infected Patients Experiencing Their First Virologic Failure While Receiving an NNRTI-containing HAART Regimen

NCT00135395

Phase 3 Completed 200 enrolled Bristol-Myers Squibb
RandomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to compare the anti-HIV efficacy, safety and effect of serum lipids of two boosted protease inhibitor-based HAART regimens (ARV/RTV v. LPV/RTV) in HIV-1 infected subjects who have experienced their first virologic failure while receiving a NNRTI-containing HAART regimen.

Timeline

Start
2004-05
Primary completion
2006-02
Completion
2006-02

Drugs

EvaluationDrugModalityDoseRoute
Comparator Atazanavir Other / unclassified 300 mg Oral
Comparator Lopinavir Other / unclassified 800 mg Oral
Comparator Ritonavir Other / unclassified 100 mg Oral
Comparator Ritonavir Other / unclassified 200 mg Oral