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Clinical trial

A Partially Blinded, Randomized, Controlled, Parallel-Group, Dose-Ranging Study to Determine the Efficacy, Safety and Tolerability of AeroFact in Preterm Infants at Risk of Worsening Respiratory Distress Syndrome

NCT03969992 is registered in ClinicalTrials.gov with Aerogen Pharma Limited as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Partially Blinded, Randomized, Controlled, Parallel-Group, Dose-Ranging Study to Determine the Efficacy, Safety and Tolerability of AeroFact in Preterm Infants at Risk of Worsening Respiratory Distress Syndrome
Lead sponsor
Aerogen Pharma Limited
Phase
Phase 2
Overall status
Completed
Start date
March 4, 2020
Completion date
August 5, 2024
Enrollment
261 (actual)
Sites
41

Conditions

As the registry lists them; a condition with its own page is linked.

respiratory distress syndrome in premature infant