drugset / Trial / NCT01797445

Study to Evaluate the Safety and Efficacy of E/C/F/TAF Versus E/C/F/TDF in HIV-1 Positive, Antiretroviral Treatment-Naive Adults

NCT01797445 ↗

Phase 3 Completed 872 enrolled Gilead Sciences
RandomizedParallel-groupDouble-blindTreatment

Summary

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

Timeline

Start
2013-03-12
Primary completion
2014-09-19
Completion
2018-10-03

Outcome

Met primary endpoint

paper E/C/F/tenofovir alafenamide was non-inferior to E/C/F/tenofovir disoproxil fumarate, with 800 (92%) of 866 patients in the tenofovir alafenamide group and 784 (90%) PMID 25890673 ↗

release “The primary endpoint was met, as E/C/F/TAF was non-inferior to Stribild” gilead.com ↗

release “in which the F/TAF-based regimen (administered as Genvoya ® ; elvitegravir 150 mg/cobicistat 150 mg/emtricitabine 200 mg/tenofovir alafenamide 10 mg, E/C/F/TAF) met its primary objective” gilead.com ↗

Publications

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