drugset / Trial / NCT00440947

Induction/Simplification With Atazanavir + Ritonavir + Abacavir/Lamivudine Fixed-Dose Combination In HIV-1 Infection

NCT00440947

Phase 3 Completed 515 enrolled ViiV Healthcare GlaxoSmithKline · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

This study was designed to test the efficacy, safety, tolerability and durability of the antiviral response between atazanavir (ATV) + ritonavir (/r) + abacavir/lamivudine(ABC/3TC) Fixed dose combination (FDC) each administered once daily (QD) for 36 weeks followed by randomization to either a simplification regimen of ATV or continuation of ATV +/r for an additional 48 weeks, each in combination with ABC/3TC in antiretroviral (ART)-naive, HIV-1 infected, HLA-B\*5701 negative subjects. All subjects who complete the 84-week study will be eligible to enter the treatment extension phase and continue for an additional 60 weeks. The purpose of this extension is to obtain longer term treatment data in subjects who have completed the 84-week study.

Timeline

Start
2007-03
Primary completion
2010-07
Completion
2010-07

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Atazanavir Other / unclassified 300 mg
Subject Atazanavir Other / unclassified 400 mg
Subject Ritonavir Other / unclassified 100 mg
Background Abacavir Other / unclassified 600 mg
Background Lamivudine Other / unclassified 300 mg