CompletedPhase 2NCT04389671
The Safety and Preliminary Tolerability of Lyophilized Lucinactant in Adults With Coronavirus Disease 2019 (COVID-19)
Studying Adult 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
- Yuh-Chin T Huang, MD, MHSDuke University
- Intervention
- Lucinactant(drug)
- Enrollment
- 20 enrolled
- Eligibility
- 18-75 years · All sexes
- Timeline
- 2021 – 2022
Study locations (11)
- University California San Diego - Jacobs Medical Center, La Jolla, California, United States
- University of California San Diego - Medical Center, Hillcrest, San Diego, California, United States
- Augusta University Health, Augusta, Georgia, United States
- University of Kentucky, Lexington, Kentucky, United States
- Tufts Medical Center, Boston, Massachusetts, United States
- Brigham and Women's Hospital, Boston, Massachusetts, United States
- Duke University Medical Center, Durham, North Carolina, United States
- Fundacion Sanatorio Güemes, Buenos Aires, Argentina
- Hospital Alemán, Buenos Aires, Argentina
- Hospital Italiano de Bueno Aires, Buenos Aires, Argentina
- CEMIC - Centro de Educacion Medica e Investigaciones Clinicals, Buenos Aires, Argentina
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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