drugset / Trial / NCT04676971

Efficacy and Safety of hzVSF-v13 in Patients With COVID-19 Pneumonia

NCT04676971

Phase 2 Completed 115 enrolled ImmuneMed, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Preliminarily investigate the safety and efficacy of two doses of hzVSF-v13 + SOC vs. placebo + SOC for the treatment of COVID-19 pneumonia.

Timeline

Start
2020-12-11
Primary completion
2021-08-29
Completion
2021-10-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Burfiralimab Monoclonal antibody 100 mg Intravenous
Subject Burfiralimab Monoclonal antibody 200 mg Intravenous

Indications