Department of Brain Health, Chambers-Grundy Center for Transformative Neuroscience, School of Integrated Health Sciences, University of Nevada Las Vegas (UNLV), Las Vegas, Nevada, USA.
Department of Brain Health, School of Integrated Health Sciences, University of Nevada Las Vegas (UNLV), Las Vegas, Nevada, USA.
Drugs. 2023 Oct;83(15):1387-1408. doi: 10.1007/s40265-023-01938-w. Epub 2023 Sep 20.
Novel agents addressing non-amyloid, non-tau targets in Alzheimer's Disease (AD) comprise 70% of the AD drug development pipeline of agents currently in clinical trials. Most of the target processes identified in the Common Alzheimer's Disease Research Ontology (CADRO) are represented by novel agents in trials. Inflammation and synaptic plasticity/neuroprotection are the CADRO categories with the largest number of novel candidate therapies. Within these categories, there are few overlapping targets among the test agents. Additional categories being evaluated include apolipoprotein E [Formula: see text] 4 (APOE4) effects, lipids and lipoprotein receptors, neurogenesis, oxidative stress, bioenergetics and metabolism, vascular factors, cell death, growth factors and hormones, circadian rhythm, and epigenetic regulators. We highlight current drugs being tested within these categories and their mechanisms. Trials will be informative regarding which targets can be modulated to produce a slowing of clinical decline. Possible therapeutic combinations of agents may be suggested by trial outcomes. Biomarkers are evolving in concert with new targets and novel agents, and biomarker outcomes offer a means of supporting disease modification by the putative treatment. Identification of novel targets and development of corresponding therapeutics offer an important means of advancing new treatments for AD.
新型药物针对阿尔茨海默病(AD)的非淀粉样蛋白、非tau 靶点,占当前临床试验中 AD 药物开发管道中的 70%。在常见阿尔茨海默病研究本体论(CADRO)中确定的大多数靶过程都由临床试验中的新型药物代表。炎症和突触可塑性/神经保护是 CADRO 中具有最大数量新型候选疗法的类别。在这些类别中,测试药物之间几乎没有重叠的靶点。正在评估的其他类别包括载脂蛋白 E [公式:见文本] 4(APOE4)效应、脂质和脂蛋白受体、神经发生、氧化应激、生物能学和代谢、血管因素、细胞死亡、生长因子和激素、昼夜节律和表观遗传调节剂。我们重点介绍了这些类别中正在测试的当前药物及其机制。这些试验将为能够调节哪些靶点以减缓临床衰退提供信息。试验结果可能会提示药物的可能联合治疗。生物标志物与新靶点和新型药物一起发展,生物标志物结果提供了一种通过潜在治疗支持疾病修饰的手段。新型靶点的鉴定和相应治疗药物的开发为 AD 的新治疗方法提供了重要手段。