TerminatedPhase 2NCT04502433
Poractant Alfa (Curosurf®)) -- Effect in Adult Patients Diagnosed With 2019 Novel Coronavirus (SARS-COV-19; (Covid-19)) Acute Respiratory Distress Syndrome (ARDS)
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
- Chiesi Farmaceutici S.p.A.
- Principal Investigator
- Clark Howard, Prof. /MDUniversity College, London
- Intervention
- CUROSURF® (poractant alfa)(drug)
- Enrollment
- 22 enrolled
- Eligibility
- 18-80 years · All sexes
- Timeline
- 2021 – 2022
Study locations (6)
- Henry Ford Health System, Detroit, Michigan, United States
- Chiesi site # 14, Bologna, Italy
- Chiesi site #13, Modena, Italy
- UCLH and UCL 250 Euston Road, London, United Kingdom
- Chiesi site #4, London, United Kingdom
- Chiesi site # 12, Southampton, United Kingdom
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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