drugset / Trial / NCT00807235

Feasibility Study of Aerosolized Surfaxin in the Prevention of Respiratory Distress Syndrome (RDS) in Premature Infants

NCT00807235

Phase 2 Terminated 17 enrolled Windtree Therapeutics
Non-randomizedParallel-groupOpen-labelPrevention

Summary

To evaluate the feasibility, safety and tolerability of aerosolized lucinactant delivered by nasal continuous positive airway pressure (nCPAP) for the prevention of respiratory distress syndrome (RDS) in premature infants.

Timeline

Start
2005-01
Primary completion
2005-08
Completion
2005-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Lucinactant Peptide 20 mg/ml Inhaled