drugset / Trial / NCT01497899

Safety and Efficacy of E/C/F/TAF (Genvoya®) Versus E/C/F/TDF (Stribild®) in HIV-1 Infected, Antiretroviral Treatment-Naive Adults

NCT01497899 ↗

Phase 2 Completed 279 enrolled Gilead Sciences
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of this study is to evaluate the efficacy of elvitegravir/cobicistat/emtricitabine/tenofovir alafenamide (Genvoya®; E/C/F/TAF) fixed-dose combination (FDC) versus elvitegravir/cobicistat/emtricitabine/tenofovir disoproxil fumarate (Stribild®; E/C/F/TDF) FDC in HIV-1 infected, antiretroviral treatment-naive adults.

Timeline

Start
2011-12-28
Primary completion
2012-10-17
Completion
2016-08-22

Drugs

EvaluationDrugModalityDoseRoute
Subject E/C/F/TAF Unknown 10 mg Oral
Subject E/C/F/TAF Unknown 150 mg Oral
Subject E/C/F/TAF Unknown 200 mg Oral
Comparator E/C/F/TDF Unknown 150 mg Oral
Comparator E/C/F/TDF Unknown 200 mg Oral
Comparator E/C/F/TDF Unknown 300 mg Oral

Indications