Cummings Jeffrey, Lee Garam, Ritter Aaron, Sabbagh Marwan, Zhong Kate
Chambers-Grundy Center for Transformative Neuroscience, Department of Brain Health School of Integrated Health Sciences University of Nevada, Las Vegas (UNLV) Las Vegas Nevada USA.
Cleveland Clinic Lou Ruvo Center for Brain Health Las Vegas Nevada USA.
Alzheimers Dement (N Y). 2020 Jul 16;6(1):e12050. doi: 10.1002/trc2.12050. eCollection 2020.
Alzheimer's disease (AD) is a growing public health concern affecting millions of patients worldwide and costing billions of dollars annually. We review the pipeline of drugs and biologics in clinical trials for the treatment of AD. We use the Common Alzheimer's and Related Dementias Research Ontology (CADRO) to classify treatment targets and mechanisms of action. We review our annual pipeline reports for the past 5 years to provide longitudinal insight into clinical trials and drug development for AD.
We reviewed ClinicalTrials.gov as of February 27, 2020, and identified all trials of pharmacologic agents currently being developed for treatment of AD as represented on this widely used U.S. Food and Drug Administration registry.
There are 121 agents in clinical trials for the treatment of AD. Twenty-nine agents are in 36 Phase 3 trials, 65 agents are in 73 Phase 2 trials, and 27 agents are in 27 Phase 1 trials. Twelve agents in trials target cognitive enhancement and 12 are intended to treat neuropsychiatric and behavioral symptoms. There are 97 agents in disease modification trials. Compared to the 2019 pipeline, there is an increase in the number of disease-modifying agents targeting pathways other than amyloid or tau.
The 2020 pipeline has innovations in clinical trials and treatment targets that provide hope for greater success in AD drug development programs. Review of clinical trials over the past 5 years show that there is progressive emphasis on non-amyloid targets, including candidate treatments for inflammation, synapse and neuronal protection, vascular factors, neurogenesis, and epigenetic interventions. There has been a marked growth in repurposed agents in the pipeline.
阿尔茨海默病(AD)是一个日益严重的公共卫生问题,影响着全球数百万患者,每年花费数十亿美元。我们回顾了用于治疗AD的临床试验中的药物和生物制剂研发进展。我们使用常见的阿尔茨海默病及相关痴呆症研究本体(CADRO)对治疗靶点和作用机制进行分类。我们回顾了过去5年的年度研发进展报告,以提供对AD临床试验和药物开发的纵向洞察。
我们检索了截至2020年2月27日的ClinicalTrials.gov,并确定了目前正在开发用于治疗AD的所有药物试验,这些试验都列在这个广泛使用的美国食品药品监督管理局登记处。
有121种药物正在进行AD治疗的临床试验。29种药物处于36项3期试验中,65种药物处于73项2期试验中,27种药物处于27项1期试验中。试验中的12种药物旨在增强认知,12种旨在治疗神经精神和行为症状。有97种药物处于疾病修饰试验中。与2019年的研发进展相比,针对淀粉样蛋白或tau以外途径的疾病修饰药物数量有所增加。
2020年的研发进展在临床试验和治疗靶点方面有创新,为AD药物开发项目取得更大成功带来了希望。对过去5年临床试验的回顾表明,越来越强调非淀粉样蛋白靶点,包括炎症、突触和神经元保护、血管因素、神经发生和表观遗传干预的候选治疗方法。研发进展中重新利用的药物有显著增长。