drugset / Trial / NCT01651637

First In Human Study on Synthetic Surfactant CHF 5633 in Respiratory Distress Syndrome

NCT01651637

Phase 1 Completed 40 enrolled Chiesi Farmaceutici S.p.A.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The aim of this study is to investigate the safety and tolerability of intratracheal administration of two different single doses of CHF 5633 in preterm neonates with RDS in terms of adverse events, adverse drug reactions, hematology and biochemistry values, the incidence of major neonatal morbidities including bronchopulmonary dysplasia (BPD) and mortality.

Timeline

Start
2012-10
Primary completion
2015-01-23
Completion
2015-01-23

Drugs

EvaluationDrugModalityDoseRoute
Subject CHF5633 Other / unclassified 100 mg/kg Other
Subject CHF5633 Other / unclassified 200 mg/kg Other