The Chambers-Grundy Center for Transformative Neuroscience, Department of Brain Health, School of Integrated Health Sciences, University of Nevada Las Vegas, and the Cleveland Clinic Lou Ruvo Center for Brain Health, Las Vegas.
J Neuropsychiatry Clin Neurosci. 2021 Winter;33(1):3-13. doi: 10.1176/appi.neuropsych.20060152. Epub 2020 Oct 28.
Alzheimer's disease (AD) is a progressive neurodegenerative disorder with limited available therapies. There is progress in developing treatments for neuropsychiatric indications in AD, including agitation, psychosis, apathy, and sleep disorders. Candidate therapies progress from nonclinical and animal assessment to trials in normal volunteers (phase 1), small phase-2 trials, and larger confirmatory phase-3 trials. Biomarkers play an increasingly important role in selecting participants, stratifying populations, demonstrating target engagement, supporting disease modification, and monitoring safety. There are currently 121 agents in clinical trials, including treatments for neuropsychiatric symptoms, cognition enhancement, and disease progression. There are 27 agents in phase-1 trials, 65 in phase-2 trials, and 29 in phase-3 trials. Most of the agents in trials (80%) target disease modification. Treatments are being assessed in secondary prevention trials with cognitively normal individuals at high risk for the development of AD. There is progress in target diversification, trial designs, outcome measures, biomarkers, and trial population definitions that promise to accelerate developing new therapies for those with or at risk for AD.
阿尔茨海默病(AD)是一种进行性神经退行性疾病,可用的治疗方法有限。在开发用于 AD 的神经精神适应症的治疗方法方面取得了进展,包括激越、精神病、淡漠和睡眠障碍。候选疗法从非临床和动物评估进展到正常志愿者的试验(第 1 阶段)、较小的第 2 阶段试验和更大的确认性第 3 阶段试验。生物标志物在选择参与者、分层人群、证明靶标结合、支持疾病修饰和监测安全性方面发挥着越来越重要的作用。目前有 121 种药物在临床试验中,包括治疗神经精神症状、认知增强和疾病进展的药物。第 1 阶段试验中有 27 种药物,第 2 阶段试验中有 65 种药物,第 3 阶段试验中有 29 种药物。试验中大多数药物(80%)的目标是疾病修饰。正在对具有认知障碍的个体进行二级预防试验,这些个体处于 AD 发病的高风险中。在目标多样化、试验设计、结局指标、生物标志物和试验人群定义方面取得了进展,有望为 AD 患者或高危患者开发新的治疗方法。