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Study identifier: NCT06694805 Synced from ClinicalTrials.gov · August 07, 2026
● Study status: Active Not Recruiting

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

Condition: HIV Infections  ·  Sponsor: ViiV Healthcare

PhasePhase 3
Planned participants326
Who can joinAll sexes, 12 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 assess how effective, safe, and long-lasting a long-acting antiretroviral therapy (ART) using CAB LA + RPV LA is for people with HIV who still have detectable virus levels despite being on oral ART. The study will also consider feedback from patients on their experience with this treatment.

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 (85)

GSK Investigational SiteBirmingham, Alabama, United States
GSK Investigational SiteLos Angeles, California, United States
GSK Investigational SiteLos Angeles, California, United States
GSK Investigational SiteLos Angeles, California, United States
GSK Investigational SiteAurora, Colorado, United States
GSK Investigational SiteDenver, Colorado, United States
GSK Investigational SiteNew Haven, Connecticut, United States
GSK Investigational SiteNewark, Delaware, United States
GSK Investigational SiteWashington D.C., District of Columbia, United States
GSK Investigational SiteJacksonville, Florida, United States
GSK Investigational SiteMiami, Florida, United States
GSK Investigational SiteSarasota, Florida, United States

+ 73 more locations — full list on the registry record.

Follow this study

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