drugset / Trial / NCT04347239

Evaluate the Efficacy & Safety of Leronlimab in Patients With Severe or Critical COVID-19

NCT04347239 ↗

Phase 2 Completed 484 enrolled CytoDyn, Inc.
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

Drugs

EvaluationDrugModalityDoseRoute
Subject Leronlimab Monoclonal antibody 700 mg Subcutaneous

Indications