CompletedPhase 2NCT02074059
Trial to Assess the Safety and Tolerability of Lucinactant for Inhalation in Premature Neonates
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
- Robert Segal, MD, FACPWindtree Therapeutics, Inc.
- Intervention
- Lucinactant for Inhalation(drug)
- Enrollment
- 80 target
- Eligibility
- All sexes
- Timeline
- 2014 – 2015
Study locations (11)
- University of Alabama at Birmingham, Birmingham, Alabama, United States
- Arkansas Children's Hospital, Little Rock, Arkansas, United States
- 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
- Riley Hospital for Children at IU Health, Indianapolis, Indiana, United States
- University of Louisville, Louisville, Kentucky, United States
- Mid Atlantic Neonatology Associates, Morristown, New Jersey, United States
- Duke University Medical Center, Durham, North Carolina, United States
- Providence St. Vincent Medical Center, Portland, Oregon, United States
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
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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