drugset / Trial / NCT04432298

Study of the Efficacy and Safety of Intravenous Pamrevlumab, in Hospitalized Participants With Acute COVID-19 Disease

NCT04432298

Phase 2 Terminated 22 enrolled Kyntra Bio
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study evaluates the efficacy and safety of intravenous (IV) infusions of pamrevlumab when compared with placebo in participants who are hospitalized with acute COVID-19 disease.

Timeline

Start
2020-06-20
Primary completion
2021-03-22
Completion
2021-03-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Pamrevlumab Monoclonal antibody 35 mg/kg Intravenous

Indications