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The crisis in recruitment for clinical trials in Alzheimer's and dementia: An action plan for solutions.阿尔茨海默病和痴呆症临床试验招募危机:解决方案行动计划
Alzheimers Dement. 2016 Nov;12(11):1113-1115. doi: 10.1016/j.jalz.2016.10.001.
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The antibody aducanumab reduces Aβ plaques in Alzheimer's disease.阿杜卡努单抗可减少阿尔茨海默病中的 Aβ 斑块。
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Why has therapy development for dementia failed in the last two decades?为什么在过去的二十年中,痴呆症的治疗方法研发失败了?
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The anatomy of medical research: US and international comparisons.医学研究的剖析:美国与国际比较。
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Mild cognitive impairment with suspected nonamyloid pathology (SNAP): Prediction of progression.疑似非淀粉样蛋白病变的轻度认知障碍(SNAP):进展预测
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Lessons from a failed γ-secretase Alzheimer trial.γ-分泌酶抑制剂阿尔茨海默病临床试验失败的教训
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A critical analysis of the 'amyloid cascade hypothesis'.对“淀粉样蛋白级联假说”的批判性分析。
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抗淀粉样β蛋白抗体的II期临床试验:何时才算足够?

Phase II clinical trials of anti-amyloid β antibodies: When is enough, enough?

作者信息

Gold Michael

机构信息

Global Product Development, Neuroscience, PPD, Morrisville, NC, USA.

出版信息

Alzheimers Dement (N Y). 2017 May 17;3(3):402-409. doi: 10.1016/j.trci.2017.04.005. eCollection 2017 Sep.

DOI:10.1016/j.trci.2017.04.005
PMID:29067346
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5651424/
Abstract

Efforts to develop new therapies to combat Alzheimer's disease suffer from extraordinarily high failure rates that make it difficult to justify continued investment in the field. Although there are a number of plausible explanations for this extremely high attrition rate, one of the explanations that has received little attention is the lack of compelling data from Phase II studies for compounds that have been pushed into Phase III trials and then have failed. An analysis of publicly available data from the Phase II studies for bapineuzumab and solanezumab indicates that neither compound produced compelling evidence of drug-like behavior that would justify their progression into pivotal trials. The published data suggest that sponsors took decisions to move these compounds into Phase III on the basis of vastly limited data that were rife with type I error and probably driven by commercial concerns. The continued push to move compounds that are not likely to succeed in later stage clinical trials threatens to erode trust in the clinical research enterprise making it much harder to properly test truly promising compounds.

摘要

开发治疗阿尔茨海默病新疗法的努力面临着极高的失败率,这使得继续在该领域投资变得难以自圆其说。尽管对于这种极高的损耗率有多种看似合理的解释,但其中一个很少受到关注的解释是,对于那些已推进到III期试验但随后失败的化合物,II期研究缺乏令人信服的数据。对巴匹兹umab和索拉珠单抗II期研究公开数据的分析表明,这两种化合物都没有产生能证明其具备类似药物行为、足以支持其进入关键试验的令人信服的证据。已发表的数据表明,申办者是基于大量存在I类错误且可能受商业利益驱动的有限数据,做出将这些化合物推进到III期的决定。持续推动那些在后期临床试验中不太可能成功的化合物进入试验,可能会侵蚀对临床研究事业的信任,从而使真正有前景的化合物更难得到妥善测试。