Condition: HIV · HIV Infections · Sponsor: ViiV Healthcare
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.
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.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
| GSK Investigational Site | Ciudad Autonoma de Buenos Aire, Argentina | — |
| GSK Investigational Site | Córdoba, Argentina | — |
| GSK Investigational Site | Antwerp, Belgium | — |
| GSK Investigational Site | Brussels, Belgium | — |
| GSK Investigational Site | Ghent, Belgium | — |
| GSK Investigational Site | Hvidovre, Denmark | — |
| GSK Investigational Site | Bordeaux, France | — |
| GSK Investigational Site | Bordeaux, France | — |
| GSK Investigational Site | Lyon, France | — |
| GSK Investigational Site | Montpellier, France | — |
| GSK Investigational Site | Nice, France | — |
| GSK Investigational Site | Nîmes, France | — |
+ 52 more locations — full list on the registry record.
Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.
We email about this public record only. Unsubscribe anytime with one click. Never medical advice. By subscribing you agree to our Terms of Use and Privacy Policy.