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Completed Phase 3 Interventional Results available

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

ClinicalTrials.gov ID: NCT05911360

Public ClinicalTrials.gov record NCT05911360. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 20, 2026, 8:15 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3b, Multicenter, Single-arm, Open-label Study Evaluating the Efficacy, Safety, and Tolerability of Switching to DTG/3TC Single Tablet Regimen Administered Once Daily From a Bictegravir/Emtricitabine/Tenofovir Alafenamide Single Tablet Regimen in People Living With HIV of at Least 50 Years of Age Who Are Virologically Suppressed

Study identification

NCT ID
NCT05911360
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
ViiV Healthcare
Industry
Enrollment
203 participants

Conditions and interventions

Interventions

  • DTG/3TC Drug

Drug

Eligibility (public fields only)

Age range
50 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 26, 2023
Primary completion
Jan 22, 2026
Completion
Feb 8, 2026
Last update posted
May 13, 2026

2023 – 2026

United States locations

U.S. sites
24
U.S. states
16
U.S. cities
24
Facility City State ZIP Site status
GSK Investigational Site Phoenix Arizona 85015
GSK Investigational Site Bakersfield California 93301
GSK Investigational Site Palm Springs California 92262
GSK Investigational Site Washington D.C. District of Columbia 20005
GSK Investigational Site Ft. Pierce Florida 34982
GSK Investigational Site Miami Florida 33133
GSK Investigational Site West Palm Beach Florida 33407
GSK Investigational Site Augusta Georgia 30912
GSK Investigational Site Decatur Georgia 30033
GSK Investigational Site Macon Georgia 31201
GSK Investigational Site Boston Massachusetts 02043
GSK Investigational Site Berkley Michigan 48072
GSK Investigational Site Detroit Michigan 48202
GSK Investigational Site Kansas City Missouri 64111
GSK Investigational Site Omaha Nebraska 68198
GSK Investigational Site Las Vegas Nevada 89106
GSK Investigational Site The Bronx New York 10467
GSK Investigational Site Charlotte North Carolina 28204
GSK Investigational Site Greensboro North Carolina 27401
GSK Investigational Site Wilmington North Carolina 28401-7684
GSK Investigational Site Akron Ohio 44304
GSK Investigational Site Portland Oregon 97239
GSK Investigational Site Philadelphia Pennsylvania 19104
GSK Investigational Site Austin Texas 78705

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 32 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05911360, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 13, 2026 · Synced May 20, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05911360 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →