{"title":"Development of monoclonal antibody therapeutics for alzheimer's disease","authors":"M. Takeda","doi":"10.4103/tpsy.tpsy_31_22","DOIUrl":null,"url":null,"abstract":"Background: In a previous review article in the Taiwanese Journal of Psychiatry (Takeda and Tagami: Taiwanese J. Psychiatry 2020; 34: 152-61), we gave the development status of drugs for Alzheimer's disease, presented a relatively pessimistic view, and highlighted the difficulties in their development. Methods: Since I have witnessed some encouraging development of monoclonal antibody therapeutics against Alzheimer's disease, I have decided to contribute this article. I reviewed new data from published journals and from internal reports of pharmaceutical companies. I have also offered some explanations and comments. Results: In 2021, I saw promising clinical trial results reporting the use of aducanumab, a monoclonal antibody treatment against amyloid β protein, and the U.S. Food and Drug Administration (FDA) announced a decision for expedited approval of aducanumab. But the results of aducanumab's phase III clinical trials were considered by some to be insufficient for the approval, and the FDA's decision was controversial. The European and Japanese regulatory authorities did not approve aducanumab. In September 2022, however, more promising results were announced from Phase III clinical trials of another monoclonal antibody, lecanemab. Conclusion: In this review, I have recounted the state of the arts of drugs for treating dementia and highlighted remarkable recent progress in the development of monoclonal antibody therapeutics for Alzheimer's disease.","PeriodicalId":22278,"journal":{"name":"Taiwanese Journal of Psychiatry","volume":"91 1","pages":"148 - 156"},"PeriodicalIF":0.0000,"publicationDate":"2022-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Taiwanese Journal of Psychiatry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/tpsy.tpsy_31_22","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background: In a previous review article in the Taiwanese Journal of Psychiatry (Takeda and Tagami: Taiwanese J. Psychiatry 2020; 34: 152-61), we gave the development status of drugs for Alzheimer's disease, presented a relatively pessimistic view, and highlighted the difficulties in their development. Methods: Since I have witnessed some encouraging development of monoclonal antibody therapeutics against Alzheimer's disease, I have decided to contribute this article. I reviewed new data from published journals and from internal reports of pharmaceutical companies. I have also offered some explanations and comments. Results: In 2021, I saw promising clinical trial results reporting the use of aducanumab, a monoclonal antibody treatment against amyloid β protein, and the U.S. Food and Drug Administration (FDA) announced a decision for expedited approval of aducanumab. But the results of aducanumab's phase III clinical trials were considered by some to be insufficient for the approval, and the FDA's decision was controversial. The European and Japanese regulatory authorities did not approve aducanumab. In September 2022, however, more promising results were announced from Phase III clinical trials of another monoclonal antibody, lecanemab. Conclusion: In this review, I have recounted the state of the arts of drugs for treating dementia and highlighted remarkable recent progress in the development of monoclonal antibody therapeutics for Alzheimer's disease.
背景:台湾精神病学杂志先前的一篇综述文章(Takeda and Tagami: taiwan J. Psychiatry 2020;(34: 152-61),我们给出了阿尔茨海默病药物的发展现状,提出了相对悲观的看法,并强调了其发展的困难。方法:由于我目睹了针对阿尔茨海默病的单克隆抗体治疗的一些令人鼓舞的发展,我决定贡献这篇文章。我从已发表的期刊和制药公司的内部报告中查阅了新的数据。我也做了一些解释和评论。结果:在2021年,我看到了有希望的临床试验结果,报告了aducanumab的使用,这是一种针对淀粉样蛋白β蛋白的单克隆抗体治疗,美国食品和药物管理局(FDA)宣布了加速批准aducanumab的决定。但一些人认为aducanumab的III期临床试验结果不足以获得批准,FDA的决定也引起了争议。欧洲和日本监管机构未批准aducanumab。然而,在2022年9月,另一种单克隆抗体lecanemab的III期临床试验公布了更有希望的结果。结论:在这篇综述中,我叙述了治疗痴呆症的药物的艺术状态,并强调了阿尔茨海默病单克隆抗体治疗的显着进展。