drugset / Trial / NCT01108510

Safety and Efficacy of COBI-boosted Atazanavir Versus Ritonavir-boosted Atazanavir Each Administered With Emtricitabine/Tenofovir Disoproxil Fumarate in HIV-1 Infected, Antiretroviral Treatment-Naive Adults

NCT01108510

Phase 3 Completed 698 enrolled Gilead Sciences
RandomizedParallel-groupTriple-blindTreatment

Summary

The objective of this study is to evaluate the safety and efficacy of a regimen containing cobicistat-boosted atazanavir (ATV+COBI) plus emtricitabine/tenofovir disoproxil fumarate (Truvada®; FTC/TDF) fixed-dose combination (FDC) versus ritonavir-boosted atazanavir (ATV+RTV) plus FTC/TDF FDC in HIV-1 infected, antiretroviral treatment-naive adults. Participants will be randomized in a 1:1 ratio. Randomization will be stratified by HIV-1 RNA level (≤ 100,000 copies/mL or \> 100,000 copies/mL) at screening.

Timeline

Start
2010-04
Primary completion
2011-11
Completion
2015-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Cobicistat Small molecule 150 mg Oral
Comparator Ritonavir Other / unclassified 100 mg Oral
Background Atazanavir Other / unclassified 300 mg Oral
Background Tenofovir disoproxil fumarate Small molecule 300 mg Oral
Background emtricitabine Other / unclassified 200 mg Oral