drugset / Trial / NCT04616586

SILtuximab in Viral ARds (SILVAR) Study

NCT04616586

Phase 3 Terminated 555 enrolled RECORDATI GROUP Syneos Health · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study will evaluate the efficacy and safety of siltuximab compared with normal saline in combination with standard of care (SOC) in selected hospitalized patients with COVID-19 previously treated with corticosteroids or another respiratory virus infection associated with acute respiratory distress syndrome (ARDS) and elevated C-reactive protein (CRP) levels.

Timeline

Start
2020-11-13
Primary completion
2021-04-01
Completion
2021-04-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Siltuximab Monoclonal antibody 11 mg/kg Intravenous