Aducanumab: A look two years after its approval

Astrid Torres, Loida Camargo, Norman López
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Abstract

Alzheimer’s disease is the leading cause of dementia worldwide and a critical public health problem. While deaths from cardiovascular diseases have decreased, those attributed to Alzheimer’s disease have increased in recent years with no curative treatment to date. In this context, effective treatment development has become a global priority. Aducanumab is a human anti-amyloid β monoclonal antibody approved by the FDA in June 2021 for the treatment of Alzheimer’s disease but failed to show the expected clinical efficacy in phase III trials. This review analyzes the history of its controversial acceptance, implications, and prospects for future treatment.

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[阿杜单抗:获批两年后的观察]。
阿尔茨海默病是全球痴呆症的主要病因,也是一个重大的公共卫生问题。虽然心血管疾病导致的死亡人数有所下降,但近年来阿尔茨海默病导致的死亡人数却在增加,而且迄今为止还没有任何治疗方法。因此,开发有效的治疗方法已成为全球的当务之急。Aducanumab 是一种人类抗淀粉样蛋白 β-淀粉样蛋白单克隆抗体,于 2021 年 6 月被美国 FDA 批准用于治疗阿尔茨海默病,但在 III 期试验中未取得预期的临床疗效。本综述讨论了该药物备受争议的接受历史、影响以及未来治疗的前景。
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