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Terminated Phase 3 Interventional

Bucillamine in Treatment of Patients With COVID-19

ClinicalTrials.gov ID: NCT04504734

Public ClinicalTrials.gov record NCT04504734. 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, 10:17 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

Multi-Center, Randomized, Double-Blind, Placebo-Controlled Study of Bucillamine in Patients With Mild-Moderate COVID-19

Brief summary

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

This is a Phase 3, multi-center, randomized, double blind, placebo controlled, clinical study of bucillamine (2 dosage levels) in patients with mild-moderate COVID-19. Patients will be randomized 1:1:1 to receive bucillamine 100 mg 3 times a day (TID), bucillamine 200 mg TID or placebo TID for up to 14 days. After the first interim analysis when a single dose is selected, patients will then be randomized 1:1 to the selected bucillamine dose or placebo. This dose has now been chosen as 600 mg. The study will be overseen by an independent Data and Safety Monitoring Board (DSMB). Up to 50 centers in the United States will conduct this study. Up to 1000 patients will be enrolled in this study. Patients will participate in the study approximately 45 days.

Study identification

NCT ID
NCT04504734
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Revive Therapeutics, Ltd.
Industry
Enrollment
713 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 80 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
Nov 27, 2020 (Actual)
Primary completion
Jun 12, 2023 (Actual)
Completion
Jun 12, 2023 (Actual)
Last update posted
Jul 7, 2023

2020 – 2023

United States locations

U.S. sites
46
U.S. states
15
U.S. cities
41
Facility City State ZIP Site status
Cullman Clinical Trials Cullman Alabama 35055 —
Avant Research Associates, LLC Huntsville Alabama 35802 —
West Valley Research Clinic Phoenix Arizona 85031 —
HealthStar Research LLC Hot Springs Arkansas 71913 —
ASCADA Research Huntington Beach California 92648 —
Samuel Ross MD Inc. Los Angeles California 90035 —
Amicis Research Center Northridge California 91324 —
Optimus Medical Group San Francisco California 94102 —
C & R Research Services USA Coral Gables Florida 33134 —
Sweet Hope Research Specialty Inc Hialeah Florida 33016 —
Encore Medical Research Hollywood Florida 33021 —
Entrust Clinical Research Kendall Florida 33156 —
Columbus Clinical Services Miami Florida 33125 —
Verus Clinical Research Miami Florida 33125 —
Nuren Medical & Research Center Miami Florida 33144 —
Advance Medical Research Services Corp Miami Florida 33165 —
Amavita Clinical Research North Miami Beach Florida 33169 —
C & R Research Services USA Tampa Florida 33614 —
Encore Medical Research of Weston LLC Weston Florida 33321 —
Clinical Site Partners LLC Winter Park Florida 32789 —
American Clinical Trials LLC Acworth Georgia 30101 —
Quad Clinical Research LLC Chicago Illinois 60643 —
Koch Family Medicine Morton Illinois 61550 —
Revive Research Institute Inc. Farmington Hills Michigan 48334 —
SRI International Plymouth Michigan 48170 —
Great Lakes Research Institute Southfield Michigan 48075 —
Revival Research Institute LLC Sterling Michigan 48312 —
Machuca Family Medicine Las Vegas Nevada 89104 —
Prime Global Research The Bronx New York 10456 —
OnSite Clinical Solutions Charlotte North Carolina 28208 —
OnSite Clinical Solutions, LLC Charlotte North Carolina 28277 —
Monroe Biomedical Research Monroe North Carolina 28112 —
Superior Clinical Research Smithfield North Carolina 27577 —
Superior Clinical Research Yanceyville North Carolina 27379 —
Dayton Clinical Research Dayton Ohio 45406 —
Pharmacorp Clinical Trials Inc. Charleston South Carolina 29412 —
Novaceut Clinical Research Clarksville Tennessee 37043 —
Physicians Quality Care Jackson Tennessee 38305 —
Inquest Clinical Research Baytown Texas 77521 —
C & R Research Services USA Houston Texas 77022 —
Encore Imaging and Medical Research Houston Texas 77065 —
R & H Clinical Research Inc. Katy Texas 77494 —
FMC Science Lampasas Texas 76550 —
Family Practice Center McAllen Texas 78501 —
R & H Clinical Research Inc. Stafford Texas 77477 —
Renovatio Clinical The Woodlands Texas 77380 —

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 NCT04504734, 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 Jul 7, 2023 · Synced Oct 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04504734 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →