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Active, not recruiting Phase 2 Interventional Results available

A Study of Teropavimab and Zinlirvimab in Combination With Capsid Inhibitor Lenacapavir in Virologically Suppressed Adults With HIV-1 Infection

ClinicalTrials.gov ID: NCT05729568

Public ClinicalTrials.gov record NCT05729568. 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 Oct 22, 2026, 10:47 PM 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 2 Randomized, Open-label Study to Evaluate the Safety and Efficacy of Broadly Neutralizing Antibodies (bNAbs) GS-5423 and GS-2872 in Combination With the Capsid Inhibitor Lenacapavir as Long-Acting Treatment Dosed Every 6 Months in Virologically Suppressed Adults With HIV-1 Infection

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The goal of this study is to test the effectiveness, safety, and tolerability of the combination of broadly neutralizing antibodies (bNAbs) (teropavimab (TAB; GS-5423) and zinlirvimab (ZAB; GS-2872)) with lenacapavir (LEN) in virologically suppressed adults with HIV-1 infection. The purpose of this study is to evaluate the efficacy of switching to a regimen of LEN, TAB and ZAB, versus continuing on baseline oral antiretroviral therapy (ART) as determined by the proportion of participants with human immunodeficiency virus-1 (HIV-1) ribonucleic acid (RNA) ≥ 50 copies/mL at Week 26.

Study identification

NCT ID
NCT05729568
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Gilead Sciences
Industry
Enrollment
83 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 65 Years
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
May 15, 2023 (Actual)
Primary completion
Jul 2, 2024 (Actual)
Completion
Dec 2030 (Estimated)
Last update posted
Apr 27, 2026

2023 – 2030

United States locations

U.S. sites
29
U.S. states
14
U.S. cities
28
Facility City State ZIP Site status
Ruane Clinical Research Group, Inc. Los Angeles California 90036 —
Mills Clinical Research Los Angeles California 90069 —
UC San Diego (UCSD) AntiViral Research Center (AVRC) San Diego California 92103 —
Optimus Medical Group San Francisco California 94102 —
University of Colorado Clinical and Translational Research Center Aurora Colorado 80045 —
Yale University; School of Medicine; AIDS Program New Haven Connecticut 06510 —
Georgetown University Medical Center Washington D.C. District of Columbia 20007 —
Midland Florida Clinical Research Center, LLC DeLand Florida 32720 —
Can Community Health Care Fort Lauderdale Florida 33316 —
Midway Immunology and Research Center Ft. Pierce Florida 34982 —
Orlando Immunology Center Orlando Florida 32803 —
Triple O Research Institute, P.A. West Palm Beach Florida 33407 —
Emory University Hospital Midtown Infectious Disease Clinic Atlanta Georgia 30308 —
Infectious Disease Specialists of Atlanta Decatur Georgia 30033 —
Southhampton Healthcare, Inc St Louis Missouri 63139 —
AXCES Research Group, LLC Albuquerque New Mexico 87109 —
Montefiore Medical Center The Bronx New York 10467 —
NC TraCS Institute - CTRC; University of North Carolina at Chapel Hill Chapel Hill North Carolina 27514 —
Duke University Health Center Durham North Carolina 27710 —
Regional Center for Infectious Disease Research Greensboro North Carolina 27401 —
The Brody School of Medicine at East Carolina University Greenville North Carolina 27858 —
Rosedale Health and Wellness Huntersville North Carolina 28078 —
Prisma Health - Clinical Research Unit Columbia South Carolina 29203 —
St Jude Children's Research Hospital Memphis Tennessee 38105 —
Central Texas Clinical Research Austin Texas 78705 —
AIDS Arms, Inc. DBA Prism Health North Texas Dallas Texas 75208 —
AXCES Research Group, LLC El Paso Texas 79902 —
The Crofoot Research Center, INC Houston Texas 77098 —
Clinical Alliance for Research & Education, Infectious Diseases LLC (CARE-ID) Annandale Virginia 22003 —

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 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05729568, 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 Apr 27, 2026 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05729568 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →