drugset / Trial / NCT05384379
Efficacy and Safety Evaluation of BZ371B in ARDS Patients
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | BZ371B | Peptide | 12 mg | Inhaled |