CompletedPhase 2NCT00455767

Safety and Efficacy Study of Depelestat in Acute Respiratory Distress Syndrome (ARDS) Patients

Studying Adult acute respiratory distress syndrome

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Key facts

Sponsor
Debiopharm International SA
Principal Investigator
François Saudubray, MD
Debiopharm SA
Intervention
EPI-hNE4(drug)
Enrollment
84 enrolled
Eligibility
18 years · All sexes
Timeline
20062007

Study locations (14)

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.

Open NCT00455767 on ClinicalTrials.gov

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