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Study identifier: NCT05979311 Synced from ClinicalTrials.gov · August 07, 2026
● Study status: Active Not Recruiting

A Study to Evaluate the Efficacy, Safety, and Tolerability of Using an Oral Once-daily 2 Drug Regimen Compared to an Oral Once-daily 3 Drug Regimen for the Treatment of Human Immunodeficiency Virus (HIV)-1 in Adults Who Have Not Previously Taken Antiretroviral Therapy

Condition: HIV · HIV Infections  ·  Sponsor: ViiV Healthcare

PhasePhase 3
Planned participants307
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

This study will compare safety, efficacy, participant reported outcomes and implementation outcomes of a fixed dose combination (FDC) of a two-drug regimen dolutegravir (DTG) plus lamivudine (3TC) and a three-drug regimen FDC of bictegravir (BIC), emtricitabine (FTC) and tenofovir alafenamide (TAF) in HIV-1 infected adult participants who have not previously received antiretroviral therapy.

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Locations (64)

GSK Investigational SiteCiudad Autonoma de Buenos Aire, Argentina
GSK Investigational SiteCórdoba, Argentina
GSK Investigational SiteAntwerp, Belgium
GSK Investigational SiteBrussels, Belgium
GSK Investigational SiteGhent, Belgium
GSK Investigational SiteHvidovre, Denmark
GSK Investigational SiteBordeaux, France
GSK Investigational SiteBordeaux, France
GSK Investigational SiteLyon, France
GSK Investigational SiteMontpellier, France
GSK Investigational SiteNice, France
GSK Investigational SiteNîmes, France

+ 52 more locations — full list on the registry record.

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