TerminatedPhase 2NCT02528318
Trial To Assess The Safety And Tolerability Of Lucinactant For Inhalation In Preterm Neonates 26 to 28 Weeks PMA
Studying Neonatal acute respiratory distress syndrome
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Windtree Therapeutics
- Principal Investigator
- Steve Simonson, MDWindtree Therapeutics
- Intervention
- Lucinactant for inhalation(combination_product)
- Enrollment
- 48 target
- Eligibility
- All sexes
- Timeline
- 2015 – 2017
Study locations (20)
- Loma Linda University Medical Center, Loma Linda, California, United States
- Sharp Mary Birch Hospital for Women and Newborns, San Diego, California, United States
- Christiana Care Health System, Newark, Delaware, United States
- University of Miami, Miami, Florida, United States
- University of Louisville, Louisville, Kentucky, United States
- University of Nebraska Medical Center, Omaha, Nebraska, United States
- Columbia University College of Physicians and Surgeons, New York Presbyterian Hospital - Morgan Stanley Children's Hospital, New York, New York, United States
- New Hanover Regional Medical Center, Wilmington, North Carolina, United States
- Providence St. Vincent Medical Center, Portland, Oregon, United States
- Women and Infants Hospital, Providence, Rhode Island, United States
- Foothills Medical Centre, Calgary, Alberta, Canada
- Royal Alexandria Hospital, Edmonton, Alberta, Canada
- Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada
- Montreal Children's Hospital, Montreal, Quebec, Canada
- Hospital Dr Sotero Del Rio, Santiago, Chile
- +5 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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