drugset / Trial / NCT02603107

Study to Evaluate the Safety and Efficacy of Switching From Regimens Consisting of Boosted Atazanavir or Darunavir Plus Either Emtricitabine/Tenofovir or Abacavir/Lamivudine to Bictegravir/Emtricitabine/Tenofovir Alafenamide in Virologically Suppressed HIV-1 Infected Adults

NCT02603107

Phase 3 Completed 578 enrolled Gilead Sciences
RandomizedParallel-groupOpen-labelTreatment

Summary

The primary objective of this study is to evaluate the efficacy of switching to a fixed-dose combination (FDC) of bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF) versus continuing on a regimen consisting of boosted atazanavir (ATV) or darunavir (DRV) plus either emtricitabine/tenofovir disoproxil fumarate (FTC/TDF) or abacavir/lamivudine (ABC/3TC) in HIV-1 infected adults who are virologically suppressed.

Timeline

Start
2015-11-20
Primary completion
2017-05-15
Completion
2019-12-23

Drugs

EvaluationDrugModalityDoseRoute
Subject bictegravir Small molecule 50 mg Oral
Subject tenofovir alafenamide Small molecule 25 mg Oral
Background Abacavir Other / unclassified 600 mg Oral
Background Atazanavir Other / unclassified 300 mg Oral
Background Cobicistat Small molecule 150 mg Oral
Background Darunavir Small molecule 800 mg Oral
Background Lamivudine Other / unclassified 300 mg Oral
Background Ritonavir Other / unclassified 100 mg Oral
Background Tenofovir disoproxil fumarate Small molecule 300 mg Oral
Background emtricitabine Other / unclassified 200 mg Oral