drugset / Trial / NCT04351152

Phase 3 Study to Evaluate Efficacy and Safety of Lenzilumab in Patients With COVID-19

NCT04351152 ↗

Phase 3 Unknown 520 enrolled Humanigen, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of this study is to assess whether the use of lenzilumab in addition to current standard of care can alleviate the immune-mediated cytokine release syndrome (CRS) and improve ventilator-free survival in hospitalized subjects with severe or critical COVID-19 pneumonia.

Timeline

Start
2020-05-05
Primary completion
2021-03
Completion
2021-03

Outcome

Met primary endpoint

paper the likelihood of survival was greater with lenzilumab than placebo (hazard ratio 1·54; 95% CI 1·02-2·32; p=0·040). PMID 34863332 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Lenzilumab Monoclonal antibody 600 mg Intravenous
Background Dexamethasone Small molecule — —
Background Remdesivir Small molecule — —

Indications