Bucillamine in Treatment of Patients With COVID-19

Phase 3

Terminated

• Conditions: Covid19
• Interventions: Drug: Bucillamine; Drug: Placebo

• Registration Number: NCT04504734
• Lead Sponsor: Revive Therapeutics, Ltd.

Brief Summary

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.

Detailed Description

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.

Patients qualifying for study enrollment will initiate therapy as outpatients, under home quarantine. Patients will receive continued standard care of therapy (per study site written policies or guidelines) together with bucillamine and/ or matching placebo for up to 14 days. Dosing should continue until the treatment course is completed or as medically indicated (e.g., deterioration of clinical status and alternative therapy required). If the patient requires hospitalization during the study period, treatment will be discontinued.

Following completion of the treatment course, follow up assessments will be performed by a study nurse 14, 28, 42, and 60 days following the end of treatment.

Up to 1000 patients will be enrolled in this study. Patients will participate in the study approximately 45 days.

Study Timeline

• Study First Submitted: 2020-08-04
• Study First Submitted QC: 2020-08-06
• Study First Posted: 2020-08-07
• Study Start: 2020-11-27
• Primary Completion: 2023-06-12
• Study Completion: 2023-06-12
• Status Verified: 2023-07
• Last Update Submitted: 2023-07-05
• Last Update Posted: 2023-07-07

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 713

Inclusion Criteria

• Is within 72 hours from onset of symptoms consistent with COVID 19 at time of study enrollment
• Has at least 2 of the following: fever (oral temperature ≥38°C), cough, shortness of breath, chest x ray changes consistent with COVID-19 at time of screening
• Has peripheral capillary oxygen saturation (SpO2) ≥94 by pulse oximetry at time of screening
• Has either a laboratory-confirmed SARS-CoV-2 infection as determined by FDA-approved rapid diagnostic (e.g., PCR) assay
• Has a score of ≤ 2 on the 8-category NIAID ordinal scale at time of screening
• Agrees to the collection of blood and urine samples, nasopharyngeal (NP) swabs, and non-invasive oxygen monitoring (via pulse oximeter) per protocol
• Patient (or their legally authorized representative) is willing and able to provide written informed consent prior to performing study procedures
• Understands and agrees to comply with planned study procedures
• Women of childbearing potential must agree to either abstinence or use at least 1 primary form of contraception not including hormonal contraception from the time of screening through Day 29 following randomization. All subjects of childbearing potential, including males with partners of childbearing potential, must use highly effective methods of birth control defined as those, alone or in combination, that result in a low failure rate (i.e., less than 1 percent per year) when used consistently and correctly. Abstinence is NOT an acceptable method of contraception UNLESS it is the subject's normal practice.

Exclusion Criteria

• Prior history of, or considered to be at risk for, agranulocytosis, nephropathy, liver disease, or interstitial pneumonia
• Serious hepatic disorder (Child-Pugh scores B or C) or alanine transaminase (ALT) or aspartate transaminase (AST) > 5 times the upper limit of normal (ULN) at screening
• Chronic kidney disease (CKD) National Kidney Foundation (NKF) stages 3B - 5 chronic renal dysfunction (estimated glomerular filtration rate [eGFR] <45 mL/min/1.73m2 according to Cockcroft Gault formula)
• Proteinuria ≥ 1+ or ≥ 30 mg on dipstick urinalysis that is confirmed on repeat assessment within 24 hours
• Serum BUN ≥ 2 × ULN or Cr ≥ 2 × ULN
• Leukopenia with absolute granulocyte count < 1500/µL
• History of positive Human Immunodeficiency virus (HIV) test or organ transplant
• Receipt of cancer chemotherapy or immunomodulatory drugs including (but not limited to) biologics such as anti-CD20, anti-TNF, anti-IL6; alkylating agents (e.g., cyclophosphamide); antimetabolites (e.g., azathioprine); or chronic corticosteroid use equivalent to prednisone >10 gm/day, during preceding 2 months
• Confirmed positive for influenza at screening
• Confirmed positive for respiratory syncytial virus (RSV) at screening
• Pregnant or breastfeeding
• Current use of, or known allergy to bucillamine or penicillamine (e.g., for Wilson's disease, rheumatoid arthritis)
• Current participation in any other clinical trial of an experimental treatment
• Receipt of any experimental treatment for COVID-19 (herbal/homeopathic, off-label, compassionate use, or trial related) within the 30 days prior to screening

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Bucillamine high dose	Bucillamine	Bucillamine 200 mg 3 times a day (TID)
Placebo	Placebo	Placebo, 3 times a day (TID)
Bucillamine low dose	Bucillamine	Bucillamine 100 mg 3 times a day (TID)

Primary Outcome Measures

Name	Time	Method
Efficacy: Frequency of hospitalization or death	From time of first dose through Day 28 following randomization	Proportion of patients meeting a composite endpoint of hospitalization or death

Secondary Outcome Measures

Name	Time	Method
Safety: Changes in adverse events from baseline to end of study	From time of first dose through Day 28 following randomization	Number of adverse events

Trial Locations

Locations (43)

Cullman Clinical Trials; 🇺🇸 Cullman, Alabama, United States

Avant Research Associates, LLC; 🇺🇸 Huntsville, Alabama, United States

West Valley Research Clinic; 🇺🇸 Phoenix, Arizona, United States

HealthStar Research LLC; 🇺🇸 Hot Springs, Arkansas, United States

ASCADA Research; 🇺🇸 Huntington Beach, California, United States

Samuel Ross MD Inc.; 🇺🇸 Los Angeles, California, United States

Amicis Research Center; 🇺🇸 Northridge, California, United States

Optimus Medical Group; 🇺🇸 San Francisco, California, United States

C & R Research Services USA; 🇺🇸 Houston, Texas, United States

Sweet Hope Research Specialty Inc; 🇺🇸 Hialeah, Florida, United States

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