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Completed Phase 2Phase 3 Interventional Results available

PRO 140 in Treatment-Experienced HIV-1 Subjects

ClinicalTrials.gov ID: NCT03902522

Public ClinicalTrials.gov record NCT03902522. 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 3, 2026, 6:53 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 Multi-center, Two-Part, Single-Arm, Open Label, 25-Week Trial With PRO 140 in Treatment-Experienced HIV-1 Subjects

Brief summary

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

The primary objectives of the trial are to assess the efficacy, clinical safety and tolerability parameters of PRO 140 in combination with failing ART (antiretroviral therapy) during the initial one-week treatment period, and in combination with Optimized Background Therapy during the subsequent 24-week treatment period.

Study identification

NCT ID
NCT03902522
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
CytoDyn, Inc.
Industry
Enrollment
6 participants

Conditions and interventions

Interventions

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
Jun 24, 2018
Primary completion
May 17, 2020
Completion
May 17, 2020
Last update posted
Sep 15, 2025

2018 – 2020

United States locations

U.S. sites
17
U.S. states
9
U.S. cities
14
Facility City State ZIP Site status
CD02_OpenLabel Investigational Site Palm Springs California 92262
CD02_OpenLabel Investigational Site San Francisco California 94115
CD02_OpenLabel Investigational Site New Haven Connecticut 06510
CD02_OpenLabel Investigational Site Ft. Pierce Florida 34982
CD02_OpenLabel Investigational Site Miami Florida 33136
CD02_OpenLabel Investigational Site Miami Florida 33139
CD02_OpenLabel Investigational Site Miami Florida 33169
CD02_OpenLabel Investigational Site Orlando Florida 32803
CD02_OpenLabel Investigational Site West Palm Beach Florida 33401
CD02_OpenLabel Investigational Site Decatur Georgia 30033
CD02_OpenLabel Investigational Site Chicago Illinois 60613
CD02_OpenLabel Investigational Site Wichita Kansas 67214
CD02_OpenLabel Investigational Site Syracuse New York 13210
CD02_OpenLabel Investigational Site Bellaire Texas 77301
CD02_OpenLabel Investigational Site Houston Texas 77004
CD02_OpenLabel Investigational Site Houston Texas 77098
CD02_OpenLabel Investigational Site Spokane Washington 99202

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03902522, 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 Sep 15, 2025 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03902522 live on ClinicalTrials.gov.

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