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This document outlines a Phase 2, randomized, double-blind, placebo-controlled study designed to evaluate the safety and efficacy of BIIB104 in subjects suffering from cognitive impairment associated with schizophrenia (CIAS). The study aims to assess various cognitive and safety parameters over a treatment duration of 12 weeks across approximately 80 global sites, involving around 219 participants. The primary objective is to evaluate changes in cognitive function as measured by the MATRICS...
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