drugset / Trial / NCT04347239
Evaluate the Efficacy & Safety of Leronlimab in Patients With Severe or Critical COVID-19
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The purpose of this study was assess the safety and efficacy of leronlimab (PRO 140) administered as weekly subcutaneous injection in subjects with severe or critical COVID-19 disease.
Timeline
- Start
- 2020-04-16
- Primary completion
- 2021-10-24
- Completion
- 2022-06-15
Publications
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Leronlimab | Monoclonal antibody | 700 mg | Subcutaneous |