drugset / Trial / NCT04460105

Lanadelumab in Participants Hospitalized With COVID-19 Pneumonia

NCT04460105

RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to evaluate the safety, pharmacokinetic and pharmacodynamics of lanadelumab administered by intravenous (IV) infusion when added to standard-of-care (SoC) in adults hospitalized with COVID-19 pneumonia.

Timeline

Start
2020-10-31
Primary completion
2021-01-27
Completion
2021-01-27

Drugs

EvaluationDrugModalityDoseRoute
Subject Lanadelumab Monoclonal antibody 300 mg Intravenous

Indications