drugset / Trial / NCT00885482

Atazanavir and Lamivudine for Treatment Simplification

NCT00885482

Phase 4 Completed 40 enrolled Catholic University of the Sacred Heart
NaSingle-groupOpen-labelTreatment

Summary

Objectives of the study: 1. To verify the safety of the study treatment, defined as the persistent control of the virus' replication at 48 weeks after the simplification to lamivudine + atazanavir with ritonavir. 2. To collect relevant information about the safety and the metabolic impact of this strategy in order to eventually design a non-inferiority randomized controlled trial for the evaluation of the safety and the efficacy of this strategy in the future.

Timeline

Start
2009-05
Primary completion
2010-05
Completion
2011-05

Drugs

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