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2019年阿尔茨海默病药物研发进程

Alzheimer's disease drug development pipeline: 2019.

作者信息

Cummings Jeffrey, Lee Garam, Ritter Aaron, Sabbagh Marwan, Zhong Kate

机构信息

Department of Brain Health, University of Nevada, Las Vegas (UNLV), School of Integrated Health Sciences, Las Vegas, NV, USA.

Cleveland Clinic Lou Ruvo Center for Brain Health, Las Vegas, NV, USA.

出版信息

Alzheimers Dement (N Y). 2019 Jul 9;5:272-293. doi: 10.1016/j.trci.2019.05.008. eCollection 2019.

Abstract

INTRODUCTION

Alzheimer's disease (AD) has few available treatments, and there is a high rate of failure in AD drug development programs. Study of the AD drug development pipeline can provide insight into the evolution of drug development and how best to optimize development practices.

METHODS

We reviewed clinicaltrials.gov and identified all pharmacologic AD trials of all agents currently being developed for treatment of AD.

RESULTS

There are 132 agents in clinical trials for the treatment of AD. Twenty-eight agents are in 42 phase 3 trials; 74 agents are in 83 phase 2 trials; and 30 agents are in 31 phase 1 trials. There is an increase in the number of agents in each phase compared with that in the 2018 pipeline. Nineteen agents in trials target cognitive enhancement, and 14 are intended to treat neuropsychiatric and behavioral symptoms. There are 96 agents in disease modification trials; of these, 38 (40%) have amyloid as the primary target or as one of several effects. Eighteen of the antiamyloid agents are small molecules, and 20 are monoclonal antibodies or biological therapies. Seven small molecules and ten biologics have tau as a primary or combination target (18%). Amyloid is the most common specific target in phase 3 and phase 2 disease modification trials. Novel biomarkers (e.g., neurofilament light), new outcomes (e.g., AD Composite Score [ADCOMS]), enrollment of earlier populations, and innovative trial designs (e.g., Bayesian adaptive designs) are new features in recent clinical trials.

DISCUSSION

Drug development continues robustly at all phases despite setbacks in several programs in the recent past. Continuing unmet needs require a commitment to growing and accelerating the pipeline.

摘要

引言

阿尔茨海默病(AD)的可用治疗方法很少,且AD药物开发项目的失败率很高。对AD药物开发流程的研究可以深入了解药物开发的演变以及如何最好地优化开发实践。

方法

我们检索了ClinicalTrials.gov,并确定了目前正在开发用于治疗AD的所有药物的所有药理学AD试验。

结果

有132种药物正在进行治疗AD的临床试验。28种药物处于42项3期试验中;74种药物处于83项2期试验中;30种药物处于31项1期试验中。与2018年的研发流程相比,每个阶段的药物数量都有所增加。试验中的19种药物旨在增强认知,14种旨在治疗神经精神和行为症状。有96种药物正在进行疾病修饰试验;其中,38种(40%)以淀粉样蛋白为主要靶点或作为多种作用之一。18种抗淀粉样蛋白药物是小分子,20种是单克隆抗体或生物疗法。7种小分子和10种生物制剂以tau蛋白作为主要或联合靶点(18%)。淀粉样蛋白是3期和2期疾病修饰试验中最常见的特定靶点。新型生物标志物(如神经丝轻链)、新的结局指标(如AD综合评分[ADCOMS])、更早人群的入组以及创新的试验设计(如贝叶斯适应性设计)是近期临床试验中的新特点。

讨论

尽管最近几个项目遭遇挫折,但药物开发在各个阶段仍在强劲推进。持续未满足的需求需要致力于扩大和加速研发流程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bde9/6617248/5a61177d9511/gr1.jpg

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