drugset / Trial / NCT03547908

Safety and Efficacy of Bictegravir/Emtricitabine/Tenofovir Alafenamide Versus Dolutegravir + Emtricitabine/Tenofovir Disoproxil Fumarate in Treatment Naive, HIV-1 and Hepatitis B Co-Infected Adults

NCT03547908

Phase 3 Completed 244 enrolled Gilead Sciences
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of this study is to evaluate the efficacy of fixed-dose combination (FDC) of bictegravir/emtricitabine/ tenofovir alafenamide (B/F/TAF) versus dolutegravir (DTG) + emtricitabine/tenofovir disoproxil fumarate (F/TDF) in treatment-naïve and HIV-1 and hepatitis B virus (HBV) adults.

Timeline

Start
2018-05-30
Primary completion
2022-02-25
Completion
2024-03-07

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject B/F/TAF Unknown 25 mg Oral
Subject B/F/TAF Unknown 50 mg Oral
Subject B/F/TAF Unknown 200 mg Oral
Comparator Dolutegravir Other / unclassified 50 mg Oral
Comparator emtricitabine/tenofovir disoproxil fumarate Unknown 200 mg Oral
Comparator emtricitabine/tenofovir disoproxil fumarate Unknown 300 mg Oral

Indications

No indication recorded.