drugset / Trial / NCT04483674

Bictegravir/FTC/TAF for the Treatment of Primary HIV Infection

NCT04483674

Phase 2 Unknown 66 enrolled Anna Cruceta
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the efficacy of Bictegravir/FTC/TAF in patients with less of 100 days post HIV infection

Timeline

Start
2020-12-04
Primary completion
2022-11
Completion
2023-06

Drugs

EvaluationDrugModalityDoseRoute
Subject bictegravir Small molecule 50 mg Oral
Subject emtricitabine Other / unclassified 200 mg Oral
Subject tenofovir alafenamide Small molecule 25 mg Oral