ClinicalTrials.gov record
Active, not recruiting Phase 2 Interventional

A Study of Islatravir (ISL) and Ulonivirine (ULO) Once Weekly (QW) in Virologically Suppressed Adults With Human Immunodeficiency Virus Type 1 (HIV-1) (MK-8591B-060)

ClinicalTrials.gov ID: NCT06891066

Public ClinicalTrials.gov record NCT06891066. 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 4, 2026, 9:47 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 2b, Randomized, Active-Controlled, Open-Label Clinical Study to Evaluate a Switch to Islatravir (ISL) and Ulonivirine (ULO) Once Weekly in Adults With HIV-1 Virologically Suppressed on Bictegravir/Emtricitabine/Tenofovir Alafenamide (BIC/FTC/TAF) Once Daily

Study identification

NCT ID
NCT06891066
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Merck Sharp & Dohme LLC
Industry
Enrollment
150 participants

Conditions and interventions

Interventions

  • BIC/FTC/TAF Drug
  • ISL Drug
  • ULO Drug

Drug

Eligibility (public fields only)

Age range
18 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
Apr 13, 2025
Primary completion
Aug 9, 2027
Completion
Sep 29, 2031
Last update posted
Oct 15, 2025

2025 – 2031

United States locations

U.S. sites
11
U.S. states
7
U.S. cities
11
Facility City State ZIP Site status
Zuckerberg San Francisco General Hospital and Trauma Center ( Site 4107) San Francisco California 94110
Mills Clinical Research ( Site 4109) West Hollywood California 90046
Georgetown University Medical Center ( Site 4106) Washington D.C. District of Columbia 20007
Orlando Immunology Center ( Site 4103) Orlando Florida 32803
Triple O Research Institute ( Site 4111) West Palm Beach Florida 33407
Chatham County Health Department - Chatham CARE Center ( Site 4116) Savannah Georgia 31401
KC CARE Health Center ( Site 4101) Kansas City Missouri 64111
Regional Center for Infectious Diseases ( Site 4115) Greensboro North Carolina 27401
Central Texas Clinical Research ( Site 4100) Austin Texas 78705
Prism Health North Texas, Oak Cliff Health Center ( Site 4114) Dallas Texas 75208
DCOL Center for Clinical Research ( Site 4112) Longview Texas 75605

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 12 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06891066, 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 Oct 15, 2025 · Synced May 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06891066 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →