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NCT00807235 · ClinicalTrials.gov registry record · Phase 2
Feasibility Study of Aerosolized Surfaxin in the Prevention of Respiratory Distress Syndrome (RDS) in Premature Infants
A Phase 2 study, sponsored by Windtree Therapeutics.
- Terminated
- Registry status
- Phase 2
- Development phase
- 17
- Enrollment target
NCT00807235: Clinical Trial Phase 2 study, sponsored by Windtree Therapeutics.
NCT00807235 is a Phase 2 study that was terminated before completion, run by Windtree Therapeutics. The registered enrollment target is 17 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (87% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00807235, a Phase 2 study, was terminated before completion, sponsored by Windtree Therapeutics.
- TERMINATED
- Registry status
- Phase 2
- Development phase
- 17 participants
- Enrollment target
Study 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.
Interventions
- DRUG Aerosolized lucinactant
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 17 participants |
| Start Date | 2005-01 |
| Est. Completion | 2005-09 |
| Phase | Phase 2 |
Why NCT00807235 stopped before completion
NCT00807235 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 17 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (87% lower).
The record links to 0 conditions, and to 1 intervention - of which Aerosolized lucinactant is the first listed.
NCT00807235 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00807235 about?
NCT00807235 is a clinical study titled "Feasibility Study of Aerosolized Surfaxin in the Prevention of Respiratory Distress Syndrome (RDS) in Premature Infants". 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.
What is the current status of trial NCT00807235?
This trial is currently terminated. It is a Phase 2 study. The enrollment target is 17 participants. The study started on 2005-01. Estimated completion is 2005-09.
What interventions are being tested in trial NCT00807235?
The interventions under investigation include: Aerosolized lucinactant (DRUG).
Who is sponsoring clinical trial NCT00807235?
This trial is sponsored by Windtree Therapeutics, which has 11 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00807235's enrollment target sits among peer trials
17 1903rd of 2000 higher than 93 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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