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Completed Phase 2 Interventional Results available

Evaluate the Efficacy & Safety of Leronlimab in Patients With Severe or Critical COVID-19

ClinicalTrials.gov ID: NCT04347239

Public ClinicalTrials.gov record NCT04347239. 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 28, 2026, 4:38 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 2b/3, Randomized, Double Blind, Placebo Controlled, Adaptive Design Study to Evaluate the Efficacy and Safety of Leronlimab for Patients With Severe or Critical Coronavirus Disease 2019 (COVID-19)

Brief summary

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

The purpose of this study was assess the safety and efficacy of leronlimab (PRO 140) administered as weekly subcutaneous injection in subjects with severe or critical COVID-19 disease.

Study identification

NCT ID
NCT04347239
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
CytoDyn, Inc.
Industry
Enrollment
484 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
Apr 16, 2020 (Actual)
Primary completion
Oct 24, 2021 (Actual)
Completion
Jun 15, 2022 (Actual)
Last update posted
Oct 15, 2025

2020 – 2022

United States locations

U.S. sites
18
U.S. states
11
U.S. cities
17
Facility City State ZIP Site status
Advanced Cardiovascular, LLC Alexander City Alabama 35010 —
St. Jude Medical Center Fullerton California 92835 —
UCLA Los Angeles California 90095 —
James A. Haley Veterans' Hospital Tampa Florida 33612 —
Center for Advanced Research & Education (CARE) Gainesville Georgia 30501 —
Beth Israel Deaconess Medical Center Boston Massachusetts 02215 —
St. Barnabas Livingston New Jersey 07052 —
Atlantic Health System Hospital Morristown New Jersey 07962-1905 —
Holy Name Medical Center Teaneck New Jersey 07666 —
New York Community Hospital of Brooklyn Brooklyn New York 11229 —
Montefiore Medical Center The Bronx New York 10467 —
Novant Health Winston-Salem North Carolina 27103 —
Ohio Health Columbus Ohio 43215 —
Good Samaritan Hospital Corvallis Corvallis Oregon 97330 —
Oregon Health and Sciences University Portland Oregon 97239 —
Baylor Scott & White Research Institute Dallas Texas 75204 —
Baylor College of Medicine Houston Texas 77030 —
University of Texas Houston Texas 77030 —

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 NCT04347239, 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 Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04347239 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →