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Completed Phase 2 Interventional Results available

Long-Acting Cabotegravir Plus VRC-HIVMAB075-00-AB (VRC07-523LS) for Viral Suppression in Adults Living With HIV-1

ClinicalTrials.gov ID: NCT03739996

Public ClinicalTrials.gov record NCT03739996. 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 Sep 2, 2026, 4:18 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 Study of Long-Acting Cabotegravir Plus VRC-HIVMAB075-00-AB (VRC07-523LS) to Maintain Viral Suppression in Adults Living With HIV-1

Brief summary

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

The purpose of this study was to assess the safety, tolerability, antiviral activity, and pharmacokinetics of long-acting cabotegravir (CAB LA) plus the broadly neutralizing monoclonal antibody VRC-HIVMAB075-00-AB (VRC07-523LS), in adults living with HIV-1 with suppressed plasma viremia.

Study identification

NCT ID
NCT03739996
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
75 participants

Conditions and interventions

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
Dec 30, 2019
Primary completion
Apr 28, 2024
Completion
Apr 28, 2024
Last update posted
May 22, 2025

2019 – 2024

United States locations

U.S. sites
17
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
Alabama CRS Birmingham Alabama 35294
UCSD Antiviral Research Center CRS San Diego California 92103
Ucsf Hiv/Aids Crs San Francisco California 94110
University of Colorado Hospital CRS Aurora Colorado 80045
Northwestern University CRS Chicago Illinois 60611
Johns Hopkins University CRS Baltimore Maryland 21205
Washington University Therapeutics (WT) CRS St Louis Missouri 63110-1010
New Jersey Medical School Clinical Research Center CRS Newark New Jersey 07103
Weill Cornell Chelsea CRS New York New York 10010
Columbia P&S CRS New York New York 10032-3732
Weill Cornell Uptown CRS New York New York 10065
University of Rochester Adult HIV Therapeutic Strategies Network CRS Rochester New York 14642
Chapel Hill CRS Chapel Hill North Carolina 27599
Cincinnati Clinical Research Site Cincinnati Ohio 45219
Ohio State University CRS Columbus Ohio 43210
Penn Therapeutics, CRS Philadelphia Pennsylvania 19104
University of Washington AIDS CRS Seattle Washington 98104-9929

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03739996, 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 22, 2025 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03739996 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →