Overview

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

Status:
Completed
Trial end date:
2007-09-01
Target enrollment:
0
Participant gender:
All
Summary
The study is aimed to assess safety of Depelestat treatment, as well as efficacy on prevention and treatment of alveolar inflammation in early pulmonary fibrosis in patients suffering from persistent Acute Respiratory Distress Syndrome.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Debiopharm International SA
Criteria
Inclusion Criteria:

- Patients suffering from persistent ARDS as defined by the American and European
Consensus Conference on ARDS, 1994

Exclusion Criteria:

- ARDS secondary to traumatism

- Pulmonary emphysema on pulmonary fibrosis

- Lung pneumocystosis

- Bronchopleural fistula

- Systemic corticosteroid treatment for more than 2 weeks before inclusion

- Severe organ disease excepted renal