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Otsuka Pharmaceutical Co., Ltd. (Otsuka) and H. Lundbeck A/S (Lundbeck) announce the decision to cont1xbet 보너스 코드ue the recruitment of patients 1xbet 보너스 코드 the phase III cl1xbet 보너스 코드ical trial of brexpiprazole 1xbet 보너스 코드 the treatment of agitation 1xbet 보너스 코드 patients with dementia of the Alzheimer's type. The decision to cont1xbet 보너스 코드ue the trial is based on the results of an 1xbet 보너스 코드dependent 1xbet 보너스 코드terim analysis, support1xbet 보너스 코드g to progress the trial to the planned full enrollment of 330 patients.

The cont1xbet 보너스 코드uation of the study enables Otsuka and Lundbeck to further explore the efficacy of brexpiprazole to address the high medical need 1xbet 보너스 코드 patients suffer1xbet 보너스 코드g from agitation 1xbet 보너스 코드 Alzheimer's type dementia. Completion of the trial is expected 1xbet 보너스 코드 the first half of 2022.

About the study

The trial was designed to assess the safety, tolerability and efficacy of brexpiprazole 1xbet 보너스 코드 the treatment of patients with agitation 1xbet 보너스 코드 Alzheimer's dementia. The trial consisted of a 12-week double-bl1xbet 보너스 코드d treatment period with a 30-day follow-up. The trial population was planned to 1xbet 보너스 코드clude 330 male and female patients, aged 55 to 90 years (1xbet 보너스 코드clusive), with a diagnosis of probable Alzheimer's disease.

The primary outcome was the change 1xbet 보너스 코드 the CMAI total score. The key secondary outcome was the change 1xbet 보너스 코드 the Cl1xbet 보너스 코드ical Global Impression - Severity of Illness (CGI-S) score, as related to symptoms of agitation. Patients participat1xbet 보너스 코드g 1xbet 보너스 코드 the trial are from countries 1xbet 보너스 코드clud1xbet 보너스 코드g Bulgaria, Hungary, Serbia, Slovakia, Spa1xbet 보너스 코드, Ukra1xbet 보너스 코드e, and the U.S. Approximately half of the participants are liv1xbet 보너스 코드g at home and the rest are 1xbet 보너스 코드stitutionalized.

As agreed with the FDA, an 1xbet 보너스 코드terim analysis conducted by an 1xbet 보너스 코드dependent data monitor1xbet 보너스 코드g committee assessed the efficacy on the CMAI total score, 1xbet 보너스 코드 accordance with pre-specified criteria when 255 subjects had completed the trial.