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Active, not recruiting Phase 3 Interventional

A Study to Evaluate the Effectiveness of Long-acting (LA) Cabotegravir (CAB) + Rilpivirine (RPV) LA When Given to Participants With Detectable HIV-1

ClinicalTrials.gov ID: NCT06694805

Public ClinicalTrials.gov record NCT06694805. 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 Jul 24, 2026, 5:49 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, Open Label, Randomized, standard-of Care Control Arm, Multicenter, Superiority Study Evaluating the Efficacy, Safety, and Tolerability of Injectable CAB LA + RPV LA in Viremic Participants Living With HIV-1 (CROWN)

Study identification

NCT ID
NCT06694805
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
ViiV Healthcare
Industry
Enrollment
326 participants

Conditions and interventions

Conditions

Interventions

  • CAB LA + RPV LA Drug
  • Oral ART Drug

Drug

Eligibility (public fields only)

Age range
12 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
Dec 1, 2024
Primary completion
Aug 18, 2026
Completion
Aug 27, 2028
Last update posted
Jul 21, 2026

2024 – 2028

United States locations

U.S. sites
39
U.S. states
21
U.S. cities
32
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35222
GSK Investigational Site Los Angeles California 90035
GSK Investigational Site Los Angeles California 90036
GSK Investigational Site Los Angeles California 90069
GSK Investigational Site Aurora Colorado 80045
GSK Investigational Site Denver Colorado 80204
GSK Investigational Site New Haven Connecticut 06510
GSK Investigational Site Newark Delaware 19711
GSK Investigational Site Washington D.C. District of Columbia 20017
GSK Investigational Site Jacksonville Florida 32209
GSK Investigational Site Miami Florida 33136
GSK Investigational Site Sarasota Florida 34237
GSK Investigational Site West Palm Beach Florida 33409
GSK Investigational Site Atlanta Georgia 30308
GSK Investigational Site Decatur Georgia 30033
GSK Investigational Site Macon Georgia 31201
GSK Investigational Site Chicago Illinois 60611
GSK Investigational Site Chicago Illinois 60613
GSK Investigational Site Chicago Illinois 60637
GSK Investigational Site Baltimore Maryland 21201
GSK Investigational Site Baltimore Maryland 21287
GSK Investigational Site Boston Massachusetts 02115
GSK Investigational Site Berkley Michigan 48072
GSK Investigational Site Kansas City Missouri 64111
GSK Investigational Site St Louis Missouri 63110
GSK Investigational Site Newark New Jersey 07102
GSK Investigational Site Hawthorne New York 10532
GSK Investigational Site New York New York 10010
GSK Investigational Site New York New York 10032
GSK Investigational Site The Bronx New York 10467
GSK Investigational Site The Bronx New York 10468
GSK Investigational Site Greensboro North Carolina 27401-1209
GSK Investigational Site Cincinnati Ohio 45267
GSK Investigational Site Columbus Ohio 43210
GSK Investigational Site Philadelphia Pennsylvania 19104
GSK Investigational Site Dallas Texas 75246
GSK Investigational Site Houston Texas 77030
GSK Investigational Site Seattle Washington 98104
GSK Investigational Site Milwaukee Wisconsin 53212

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 46 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06694805, 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 Jul 21, 2026 · Synced Jul 24, 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 NCT06694805 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →