Last updated on January 2020

A Study to Evaluate the Efficacy and Safety of BIIB093 in Participants With Brain Contusion


Brief description of study

The primary objective is to determine if BIIB093 reduces brain contusion expansion by Hour 96 when compared to placebo.

The secondary objectives are to evaluate the effects of BIIB093 on acute neurologic status, functional outcomes, and treatment requirements, to further differentiate the mechanism of action of BIIB093 on contusion expansion by examining differential effects on hematoma and edema expansion, and to determine if BIIB093 improves survival at Day 90 when compared to placebo.

Clinical Study Identifier: NCT03954041

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Bunkyo-ku, Japan
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