Project Details
Description
A Partially-Blind, Randomized, Parallel-Group Dose Ranging Study to Determine the Efficacy, Safety and Tolerability of AeroFact (Aerosolized SF-RI 1) Administered by nCPAP versus nCPAP alone in the Treatment of Preterm Infants at Risk for Worsening Res
| Status | Active |
|---|---|
| Effective start/end date | 4/23/19 → 4/30/24 |
Funding
- AEROGEN, INC
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