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未能证明 aducanumab 的疗效:Biogen 报告的 EMERGE 和 ENGAGE 试验分析,2019 年 12 月。

Failure to demonstrate efficacy of aducanumab: An analysis of the EMERGE and ENGAGE trials as reported by Biogen, December 2019.

机构信息

Department of Neurology, Mayo Clinic, Rochester, Minnesota, USA.

Department of Radiology, Mayo Clinic, Rochester, Minnesota, USA.

出版信息

Alzheimers Dement. 2021 Apr;17(4):696-701. doi: 10.1002/alz.12213. Epub 2020 Nov 1.

Abstract

Aducanumab recently underwent two large phase III clinical trials that were stopped prematurely by the sponsor Biogen. One trial was trending positive while the other showed no benefits from aducanumab. Post hoc analyses led the sponsor to assert that there was a sufficient efficacy signal to justify a new drug application as a treatment for Alzheimer's disease. The sponsor claimed that subsets of participants receiving sufficiently high doses of aducanumab demonstrated benefits in both trials. In contrast, we identified alternative accounts for the apparent drug benefits in post hoc subgroups that are unrelated to dose effects. Biomarker data were consistent with target engagement, but no evidence was presented to correlate biomarker changes to cognitive benefits. Our analysis supports the conduct of a third, phase III trial with high-dose aducanumab. Aducanumab's efficacy as a treatment for the cognitive dysfunction in Alzheimer's disease cannot be proven by clinical trials with divergent outcomes.

摘要

阿杜卡努单抗最近进行了两项由赞助商百健公司提前终止的大型三期临床试验。一项试验呈阳性趋势,而另一项试验则显示阿杜卡努单抗没有获益。事后分析导致赞助商断言,有足够的疗效信号证明可以作为治疗阿尔茨海默病的新药申请。赞助商声称,接受足够高剂量阿杜卡努单抗的参与者亚组在两项试验中均显示出获益。相比之下,我们为事后亚组中明显的药物获益找到了替代解释,这些解释与剂量效应无关。生物标志物数据与靶标结合一致,但没有证据表明生物标志物的变化与认知获益相关。我们的分析支持进行第三次、高剂量阿杜卡努单抗的三期试验。临床试验结果不一致,无法证明阿杜卡努单抗治疗阿尔茨海默病认知功能障碍的疗效。

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