drugset / Trial / NCT02607930

Study to Evaluate the Safety and Efficacy of Bictegravir/Emtricitabine/Tenofovir Alafenamide Versus Abacavir/Dolutegravir/Lamivudine in Human Immunodeficiency Virus-1 (HIV-1) Infected, Antiretroviral Treatment-Naive Adults

NCT02607930 ↗

Phase 3 Completed 631 enrolled Gilead Sciences
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of this study is to evaluate the efficacy of a fixed dose combination (FDC) containing bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF) versus a FDC containing abacavir/dolutegravir/lamivudine (ABC/DTG/3TC) in HIV-1 infected, antiretroviral treatment naive-adults.

Timeline

Start
2015-11-13
Primary completion
2017-05-09
Completion
2021-07-02

Outcome

Met primary endpoint

paper difference -0·6%, 95·002% CI -4·8 to 3·6; p=0·78), demonstrating non-inferiority of bictegravir, emtricitabine, and tenofovir alafenamide PMID 28867497 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator ABC/DTG/3TC Unknown — Oral
Subject B/F/TAF Unknown — Oral