drugset / Trial / NCT04380961

A Study to Evaluate the Efficacy and Safety of Sirukumab in Confirmed Severe or Critical Confirmed Coronavirus Disease (COVID)-19

NCT04380961

Phase 2 Completed 212 enrolled Janssen Pharmaceutica N.V., Belgium
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the clinical response of sirukumab (administered as a single intravenous dose) plus standard of care (SOC) compared to placebo plus SOC in COVID-19.

Timeline

Start
2020-04-24
Primary completion
2021-04-09
Completion
2021-06-24

Drugs

EvaluationDrugModalityDoseRoute
Subject Sirukumab Monoclonal antibody Intravenous

Indications