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Current Clinical Trials in the Treatment of Alzheimer's Disease Akira Tamaoka 1 1Department of Neurology, Division of Clinical Medicine, University of Tsukuba Keyword: アルツハイマー病 , コリン仮説 , アミロイド仮説 , アミロイドβ蛋白 , タウ蛋白 , バイオマーカー , モノクローナル抗体 , Alzheimer's disease , cholinergic hypothesis , amyloid hypothesis , amyloid-β protein , tau protein , biomarker , monoclonal antiboies pp.23-34
Published Date 2020/1/1
DOI https://doi.org/10.11477/mf.1416201475
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Abstract

There is an urgent need for Alzheimer's disease (AD) treatments because of the growing number of individuals with preclinical, prodromal, and dementia forms of AD. Unfortunately, there are few effective treatments for AD, and many drug development trials for AD ultimately have failed. Current AD clinical trials include disease-modifying therapies, symptomatic cognitive enhancers, and symptomatic agents addressing neuropsychiatric and behavioral changes. Disease modifying therapies include anti-amyloid agents and anti-tau agents, both of which contain small molecules, monoclonal antibodies, or biological therapies. Amyloid is the most common specific target in phase 3 and phase 2 disease modification trials. Recent drug development trials for AD include preclinical and prodromal populations. Although biomarkers are increasingly used in drug development for AD, they are not used uniformly for confirmation of AD diagnosis. Enrollment of earlier populations, new biomarkers (e.g., neurofilament light), novel outcomes (e.g., AD Composite Score [ADCOMS]), and innovative trial designs (e.g., futility analysis, Bayesian adaptive designs) are needed to develop effective drugs against AD.


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電子版ISSN 1344-8129 印刷版ISSN 1881-6096 医学書院

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