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VentaProst Versus Conventionally-Administered Aerosolized Epoprostenol in Patients Undergoing Cardiac Surgery With CPB
The purpose of the Phase 2a study is to: 1) demonstrate that the estimated VentaProst dose is safe and equivalent in effect to a dose administered via epoprostenol aerosolization by the current off-label-use practice; and 2) demonstrate that an optimum effect can be rapidly obtained with VentaProst titration.
Details
| Lead sponsor | Aerogen Pharma Limited |
|---|---|
| Phase | PHASE2 |
| Status | COMPLETED |
| Enrolment | 17 |
| Start date | Wed Aug 23 2017 00:00:00 GMT+0000 (Coordinated Universal Time) |
| Completion | Thu May 30 2019 00:00:00 GMT+0000 (Coordinated Universal Time) |
Conditions
- Pulmonary Hypertension
Interventions
- VentaProst
Countries
United States