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VentaProst Versus Conventionally-Administered Aerosolized Epoprostenol in Patients Undergoing Cardiac Surgery With CPB

NCT03122730 PHASE2 COMPLETED Results posted

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 sponsorAerogen Pharma Limited
PhasePHASE2
StatusCOMPLETED
Enrolment17
Start dateWed Aug 23 2017 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionThu May 30 2019 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions

Countries

United States