The Safety and Efficacy of Lucinactant for Inhalation in Premature Neonates 26 to 32 Weeks Gestational Age

Key facts

Sponsor

Windtree Therapeutics

Principal Investigator

Steven Simonson, MD

Windtree Therapeutics

Intervention

Lucinactant delivered via investigational delivery device(drug)

Enrollment

221 enrolled

Eligibility

All sexes

Timeline

2015 – 2019

Study locations (30)

• University of Alabama at Birmingham, Birmingham, Alabama, United States
• Univ. of Arkansas Medical Center, Little Rock, Arkansas, United States
• Loma Linda University Medical Center, Loma Linda, California, United States
• Children's Hospital of Orange County, Orange, 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 Holtz Children's Hospital, Miami, Florida, United States
• University of Michigan Health System, Ann Arbor, Michigan, United States
• University of Mississippi Medical Center, Jackson, Mississippi, United States
• University of Nebraska Medical Center, Omaha, Nebraska, United States
• Albany Medical Center, Albany, New York, United States
• Morgan Stanley Childrens Hospital of New York Presbyterian (CHONY), New York, New York, United States
• Duke University Medical Center, Durham, North Carolina, United States
• Brody School of Medicine at ECU, Greenville, North Carolina, United States
• New Hanover Regional Medical Center, Wilmington, North Carolina, United States
• +15 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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