- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04901676
Leronlimab in Moderately Ill Patients With COVID-19 Pneumonia
A Phase 3, Randomized, Double Blind, Placebo Controlled Trial to Evaluate the Efficacy and Safety of Leronlimab in Combination With Standard of Care for Moderately Ill Patients With Coronavirus Disease 2019 (COVID-19) Pneumonia
Leronlimab (PRO 140) is a humanized IgG4,k monoclonal antibody (mAb) that recognizes the C-C chemokine receptor type 5 (CCR5). Disruption of the C-C chemokine ligand 5 (CCL5)-CCR5 axis via leronlimab-mediated CCR5 blockade might prevent pulmonary trafficking of pro-inflammatory leukocytes and dampen pathogenic immune activation in coronavirus disease 2019 (COVID-19).
The purpose of the study is to assess the safety and efficacy of leronlimab plus standard of care in patients hospitalized with COVID-19 pneumonia who are not requiring mechanical ventilation or extracorporeal oxygenation (ECMO).
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Leronlimab (PRO 140) is a humanized IgG4,k monoclonal antibody (mAb) that recognizes the C-C chemokine receptor type 5 (CCR5). CCR5 is expressed predominantly on T cells but also found on macrophages, dendritic cells, and eosinophils to mediate chemotaxis in response to its cognate ligands that include CCL5 (RANTES), CCL3 (MIP-1α), and CCL4 (MIP-1β). These ligands are integral in the recruitment of these immune cells to inflammatory sites. The immunopathogenesis of COVID-19 likely involves the excessive influx of immune cells into the lung. Disruption of the CCL5-CCR5 axis via leronlimab-mediated CCR5 blockade might prevent pulmonary trafficking of pro-inflammatory leukocytes and dampen pathogenic immune activation in COVID-19.
The purpose of the study is to assess the safety and efficacy of leronlimab plus standard of care in patients hospitalized with COVID-19 pneumonia who are not requiring mechanical ventilation or extracorporeal oxygenation (ECMO).
This is a Phase 3, 2-arm, randomized, double blind, placebo controlled, multicenter study to evaluate the safety and efficacy of leronlimab (PRO 140) as an add on therapy to the institutional standard of care (SoC) for the management of moderately ill patients with COVID-19 pneumonia.
Patients will be randomized in a 1:1 ratio to receive up to four doses of leronlimab (PRO 140) or placebo. Leronlimab (700 mg followed by 350 mg weekly) or placebo will be administered subcutaneously over a 4-week treatment period. No treatments will be administered post-discharge.
The participant will be evaluated on each study day while hospitalized up until and including Day 28. The daily visits will capture clinical status - ordinal scale and the occurrence of adverse events. A complete follow-up assessment will be performed at Days 7, 14, 21, 28, 42 and 60 for those who are hospitalized at these specific timepoints. Follow-up visits can be conducted as telephone or video contact visits, if subject is discharged from the hospital prior to the complete follow-up visits.
Study Type
Enrollment (Anticipated)
Phase
- Phase 3
Contacts and Locations
Study Locations
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-
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Sao Paulo, Brazil
- Hospital Israelita Albert Einstein
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BA
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Ipiaú, BA, Brazil
- Clinica São Roque
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Salvador, BA, Brazil
- Santa Casa de Misericórdia da Bahia - Hospital Santa Izabel
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Salvador, BA, Brazil
- Instituto de Ensino e Pesquisa do Hospital da Bahia
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DF
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Brasília, DF, Brazil
- Hospital do Coração do Brasil
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ES
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Vitória, ES, Brazil
- Hospital Vitoria
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MG
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Belo Horizonte, MG, Brazil
- Hospital Felicio Rocho
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Passos, MG, Brazil
- Santa Casa de Passos
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RJ
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Rio De Janeiro, RJ, Brazil
- Hospital São Lucas Copacabana
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RN
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Natal, RN, Brazil
- Instituto Atena de Pesquisa Clínica
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-
RS
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Passo Fundo, RS, Brazil
- Hospital São Vicente de Paulo
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Porto Alegre, RS, Brazil
- Hospital Mae de Deus
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Porto Alegre, RS, Brazil
- Irmandade da Santa Casa de Misericórdia Porto Alegre
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SE
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Aracaju, SE, Brazil
- Centro de Pesquisa Clinica do Coracao
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SP
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Barretos, SP, Brazil
- Fundação PIO XII
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Bragança Paulista, SP, Brazil
- Irmandade do Sr. Bom Jesus dos Passos da Santa Casa de Misericórdia de Bragança Paulista
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Campinas, SP, Brazil
- Instituto de Pesquisa Clínica de Campinas
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Santos, SP, Brazil
- Santa Casa de Santos
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Sao Paulo, SP, Brazil
- BP Mirante
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São José Do Rio Preto, SP, Brazil
- Fundação Faculdade Regional de Medicina de São José do Rio Preto
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São Paulo, SP, Brazil
- Hospital Alemao Oswaldo Cruz
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São Paulo, SP, Brazil
- Hospital Santa Paula
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São Paulo, SP, Brazil
- Hospital Beneficência Portuguesa
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São Paulo, SP, Brazil
- Associação Beneficente Síria - Hospital do Coração (HCor)
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São Paulo, SP, Brazil
- Hospital 9 De Julho
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São Paulo, SP, Brazil
- Hospital M'Boi Mirim
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São Paulo
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Votuporanga, São Paulo, Brazil
- Santa Casa de Votuporanga
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Male or females aged ≥ 18 years
- Moderately ill patients with COVID-19 (defined as Ordinal Scale of 5 or 6): Hospitalized, requiring supplemental oxygen or hospitalized, on non-invasive ventilation or high flow oxygen devices
- Evidence of pneumonia (pulmonary infiltrates) at chest radiography or computed tomography compatible with COVID-19.
- Hospitalization for less than 72 hours, receiving standard of care treatment for COVID-19.
- Laboratory-confirmed novel coronavirus (SARS-CoV-2) infection as determined by polymerase chain reaction (PCR).
- Subject (or legally authorized representative) provides written or oral informed consent prior to initiation of any study procedures.
- Women of childbearing potential and their partner must agree to use at least one highly effective method of contraception (e.g., hormonal contraceptives [implants, injectables, combination oral contraceptives, transdermal patches, or contraceptive rings], intrauterine devices, bilateral tubal occlusion, or sexual abstinence) for the duration of the study.
Exclusion Criteria:
- Subjects on invasive mechanical ventilation or extracorporeal membrane oxygenation (ECMO).
- Subjects who have a history of allergic reactions attributed to compounds of similar chemical or biologic composition to leronlimab (PRO 140) are not eligible.
- Inability to provide informed consent (from subject or legally authorized representative) or to comply with test requirements.
- Other medical or psychiatric condition including recent (within the past year) or active suicidal ideation/behavior or laboratory abnormality that may increase the risk associated with study participation or, in the investigator's judgment, make the participant inappropriate for the study.
- Pregnancy or breast feeding.
- Subject participating in another study with for an investigational treatment.
- Suspected or known active systemic bacterial, fungal, or viral infections (with the exception of COVID-19), that may increase the risk for the study participant based on investigator judgement.
- Participants who are immunocompromised, with known immunodeficiencies, or taking potent immunosuppressive agents (e.g., azathioprine, cyclosporine).
- Patients with estimated discharge or transfer for other hospital in the first 72 hours of study inclusion.
- Patients with low probability of survival in the first 48 hours of study inclusion.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Leronlimab
Leronlimab subcutaneously once a week (up to 4 doses) until hospital discharge.
The first dose will be of 700 mg, followed by weekly doses of 350 mg.
|
Leronlimab 700 mg (first dose) followed by weekly 350 mg
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Placebo Comparator: Placebo
Placebo subcutaneously once a week (up to 4 doses) until hospital discharge
|
Placebo
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Cumulative incidence of death or respiratory failure until day 28
Time Frame: 28 days
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Rates of participants who attain categories 6, 7, or 8 on the eight-category ordinal scale within 28 days
|
28 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Time to clinical recovery
Time Frame: 28 days
|
Categories 1, 2 and 3 on a 8-point ordinal scale
|
28 days
|
Death or intubation until day 28
Time Frame: 28 days
|
Categories 7 or 8 on the eight-point ordinal scale
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28 days
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Proportion of patients clinically recovered
Time Frame: Days 14, 28, 42, and 60
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Categories 1, 2 and 3 on a 8-point ordinal scale
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Days 14, 28, 42, and 60
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All-cause mortality
Time Frame: Days 14, 28, 42, and 60
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Days 14, 28, 42, and 60
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Proportion of patients discharged alive
Time Frame: Days 14, 28, 42, and 60
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Categories 1 and 2 on a 8-point ordinal scale
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Days 14, 28, 42, and 60
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Clinical status
Time Frame: Days 14, 28, 42, and 60
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On a 8 point ordinal scale
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Days 14, 28, 42, and 60
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Length of hospital stay
Time Frame: 28 days
|
days
|
28 days
|
Collaborators and Investigators
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Coronavirus Infections
- Coronaviridae Infections
- Nidovirales Infections
- RNA Virus Infections
- Virus Diseases
- Infections
- Respiratory Tract Infections
- Respiratory Tract Diseases
- Pneumonia, Viral
- Lung Diseases
- COVID-19
- Pneumonia
- Molecular Mechanisms of Pharmacological Action
- Anti-Infective Agents
- Antiviral Agents
- Anti-HIV Agents
- Anti-Retroviral Agents
- HIV Fusion Inhibitors
- Viral Fusion Protein Inhibitors
- Leronlimab
Other Study ID Numbers
- ARO_21_018_001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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