drugset / Trial / NCT01095796

Study to Evaluate the Safety and Efficacy of Stribild Versus Atripla in Human Immunodeficiency Virus, Type 1 (HIV-1) Infected, Antiretroviral Treatment-Naive Adults

NCT01095796 ↗

Phase 3 Completed 707 enrolled Gilead Sciences
RandomizedParallel-groupQuadruple-blindTreatment

Summary

To evaluate the safety and efficacy of Stribild®, a single tablet regimen (STR) containing fixed doses of elvitegravir (EVG)/cobicistat (COBI \[GS-9350\])/emtricitabine (FTC)/tenofovir disoproxil fumarate (TDF) versus efavirenz (EFV)/FTC/TDF (Atripla®) in HIV-1 infected, antiretroviral treatment-naive adults. Stribild offers an alternative STR for patients who are not candidates for non-nucleoside reverse transcriptor-based STRs.

Timeline

Start
2010-03
Primary completion
2011-08
Completion
2014-09

Outcome

Met primary endpoint

paper EVG/COBI/FTC/TDF was non-inferior to EFV/FTC/TDF; 305/348 (87·6%) versus 296/352 (84·1%) PMID 22748591 ↗

release “Stribild met its primary objective of non-inferiority compared to Atripla ® (efavirenz 600 mg/emtricitabine 200 mg/tenofovir disoproxil (as fumarate) 300 mg) (Study 102)” gilead.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Atripla Unknown — Oral
Subject Stribild Other / unclassified — Oral