Holmusk, New York, NY, USA.
Neuroscience Development, AbbVie, North Chicago, IL, USA.
J Alzheimers Dis. 2022;87(1):83-100. doi: 10.3233/JAD-215699.
Given the acknowledged lack of success in Alzheimer's disease (AD) drug development over the past two decades, the objective of this review was to derive key insights from the myriad failures to inform future drug development. A systematic and exhaustive review was performed on all failed AD compounds for dementia (interventional phase II and III clinical trials from ClinicalTrials.gov) from 2004 to the present. Starting with the initial ∼2,700 AD clinical trials, ∼550 trials met our initial criteria, from which 98 unique phase II and III compounds with various mechanisms of action met our criteria of a failed compound. The two recent reported phase III successes of aducanumab and oligomannate are very encouraging; however, we are awaiting real-world validation of their effectiveness. These two successes against the 98 failures gives a 2.0% phase II and III success rate since 2003, when the previous novel compound was approved. Potential contributing methodological factors for the clinical trial failures were categorized into 1) insufficient evidence to initiate the pivotal trials, and 2) pivotal trial design shortcomings. Our evaluation found that rational drug development principles were not always followed for AD therapeutics development, and the question remains whether some of the failed compounds may have shown efficacy if the principles were better adhered to. Several recommendations are made for future AD therapeutic development. The whole database of the 98 failed compounds is presented in the Supplementary Material.
鉴于过去二十年中阿尔茨海默病(AD)药物开发的公认失败,本综述旨在从众多失败中汲取关键见解,为未来的药物开发提供信息。对 2004 年至今来自 ClinicalTrials.gov 的所有针对痴呆症的失败 AD 化合物(干预性 II 期和 III 期临床试验)进行了系统和详尽的审查。从最初的约 2700 项 AD 临床试验开始,约有 550 项试验符合我们的初始标准,其中 98 种具有不同作用机制的独特 II 期和 III 期化合物符合我们失败化合物的标准。最近报告的 aducanumab 和 oligomannate 的两项 III 期成功非常令人鼓舞;然而,我们仍在等待它们有效性的实际验证。这两项成功与 98 项失败相比,自 2003 年以来 II 期和 III 期的成功率为 2.0%,当时上一个新化合物获得批准。将临床试验失败的潜在相关方法因素分为 1)启动关键试验的证据不足,以及 2)关键试验设计缺陷。我们的评估发现,AD 治疗药物开发并不总是遵循合理的药物开发原则,并且仍存在一些疑问,即如果更好地遵守这些原则,一些失败的化合物是否可能显示出疗效。为未来的 AD 治疗开发提出了一些建议。98 种失败化合物的整个数据库都在补充材料中呈现。