drugset / Trial / NCT05384379

Efficacy and Safety Evaluation of BZ371B in ARDS Patients

NCT05384379 ↗

NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate safety, tolerability and efficacy of BZ371B in intubated patients with severe Acute Respiratory Distress Syndrome.

Timeline

Start
2022-11-23
Primary completion
2023-03-03
Completion
2023-03-03

Outcome

Outcome not reported

Stopped (Enrollment): “Suboptimal enrollment”

Drugs

EvaluationDrugModalityDoseRoute
Subject BZ371B Peptide 12 mg Inhaled