drugset / Trial / NCT04449588

Efficacy and Safety Study of BDB-001 in Severe COVID-19 With ALI/ARDS

NCT04449588

RandomizedParallel-groupOpen-labelTreatment

Summary

This multi-center, open, randomized study will evaluate the efficacy and safety of BDB-001 injection in severe COVID-19 with severe pneumonia, or acute lung injury/acute respiratory distress syndrome. Patients will be randomized to two treatment arms (Arm A: Conventional treatment + BDB-001; Arm B: Conventional treatment alone).

Timeline

Start
2020-07-23
Primary completion
2024-03-26
Completion
2024-03-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Resiquimod Small molecule

Indications