drugset / Trial / NCT04901676
Leronlimab in Moderately Ill Patients With COVID-19 Pneumonia
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Leronlimab | Monoclonal antibody | 350 mg | Subcutaneous |