drugset / Trial / NCT05911360

A Study to Evaluate Efficacy, Safety and Tolerability in Antiretroviral Therapy (ART)-Experienced Participants of at Least 50 Years of Age Living With Human Immunodeficiency Virus (HIV) With Virologic Suppression Who Switch to DTG/3TC FDC From BIC/FTC/TAF

NCT05911360

Phase 3 Completed 205 enrolled ViiV Healthcare
NaSingle-groupOpen-labelTreatment

Summary

The study aims at evaluating the maintenance of virologic suppression of dolutegravir/lamivudine (DTG/3TC) fixed dose combination (FDC) at Week 48 post-switch from bictegravir/emtricitabine/tenofovir alafenamide (BIC/FTC/TAF) in participants living with Human Immunodeficiency Virus Type 1 (HIV-1) who are of at least 50 years of age and above.

Timeline

Start
2023-07-07
Primary completion
2026-01-23
Completion
2026-02-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Dolutegravir Other / unclassified
Subject Lamivudine Other / unclassified