drugset / Trial / NCT01495702

Study to Evaluate Switching From Regimens Consisting of a Nonnucleoside Reverse Transcriptase Inhibitor Plus Emtricitabine and Tenofovir DF to the Elvitegravir/Cobicistat/Emtricitabine/Tenofovir DF Single-Tablet Regimen in Virologically Suppressed, HIV-1 Infected Patients

NCT01495702 ↗

Phase 3 Completed 439 enrolled Gilead Sciences
RandomizedParallel-groupOpen-labelTreatment

Summary

This study will evaluate the noninferiority of Stribild® (elvitegravir/cobicistat/emtricitabine/tenofovir disoproxil fumarate (E/C/F/TDF)) single-tablet regimen (STR) relative to regimens consisting of a nonnucleoside reverse transcriptase inhibitor (NNRTI) plus Truvada® (FTC/TDF) in maintaining HIV-1 RNA \< 50 copies/mL at Week 48 in virologically suppressed, HIV-1 infected adults. This study will also evaluate the safety, tolerability, and efficacy of the two regimens through 96 weeks of treatment.

Timeline

Start
2011-12
Primary completion
2013-11
Completion
2014-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Cobicistat Small molecule 150 mg Oral
Subject Tenofovir disoproxil fumarate Small molecule 300 mg —
Subject Tenofovir disoproxil fumarate Small molecule 300 mg Oral
Subject elvitegravir Small molecule 150 mg Oral
Subject emtricitabine Other / unclassified 200 mg —
Subject emtricitabine Other / unclassified 200 mg Oral
Comparator Efavirenz Other / unclassified — —
Comparator Nevirapine Small molecule — —
Comparator Rilpivirine Small molecule — —

Indications