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Comparison of the efficacy and safety of FP 1201 lyo (intravenously administered recombinant human interferon beta 1a) and placebo in the treatment of patients with moderate or severe acute respiratory distress syndrome: study protocol for a randomized co

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Figure

Table 1 The Berlin ARDS definition [1]
Fig. 1 Study design. aNot more than 48 h may elapse between confirmation of moderate or severe acute respiratory distress syndrome (ARDS)during screening and administration of the first dose of study drug on day 1
Fig. 2 Schedule of procedures.SOFAInterferon,EuroQolPhysiology and Chronic Health Evaluation,for patients withdrawing from the study before D28

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