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Fig. 1 | Trials

Fig. 1

From: 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 controlled trial

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. Once eligibility has been met, randomization can occur during screening or pre-dose on day 1

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Trials

ISSN: 1745-6215