drugset / Trial / NCT04901676

Leronlimab in Moderately Ill Patients With COVID-19 Pneumonia

NCT04901676 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

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).

Timeline

Start
2021-09-09
Primary completion
2023-01
Completion
2023-02

Outcome

Outcome not reported

Stopped: “Pending DSMB evaluation”

Drugs

EvaluationDrugModalityDoseRoute
Subject Leronlimab Monoclonal antibody 350 mg Subcutaneous

Indications