[Translation] An 18-month placebo-controlled, double-blind, parallel-group study with an open-label extension to confirm the safety and efficacy of BAN2401 in patients with early AD
主要目的 通过确定BAN2401在治疗18个月时临床痴呆评定量表总分(CDR-SB)相对于基线的变化方面优于安慰剂而评估BAN2401在患有早期阿尔茨海默病(EAD)的受试者中的疗效
[Translation] Primary Objective To evaluate the efficacy of BAN2401 in subjects with early Alzheimer's disease (EAD) by determining the superiority of BAN2401 over placebo in the change from baseline in the Clinical Dementia Rating Scale-SB score (CDR-SB) at 18 months of treatment