drugset / Trial / NCT04460105
Lanadelumab in Participants Hospitalized With COVID-19 Pneumonia
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Lanadelumab | Monoclonal antibody | 300 mg | Intravenous |