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从失败的阿尔茨海默病试验中可以吸取哪些教训?

What lessons can be learned from failed Alzheimer's disease trials?

作者信息

Toyn Jeremy

机构信息

Pharmaceutical and Biotechnology Consultant, P.O. Box 11, Belmont, MA 02478, USA.

出版信息

Expert Rev Clin Pharmacol. 2015 May;8(3):267-9. doi: 10.1586/17512433.2015.1034690. Epub 2015 Apr 10.

Abstract

Trials missing primary efficacy end points raise the question of whether the choice of drug or the limitations of disease biology were at fault. In some trials, drugs appear not to have achieved biochemical effect thresholds sufficient for clinical benefit. This suggests the need for improved drugs that are more active at tolerated doses. In other trials, it is unclear how the observed biomarker changes are related to potential efficacy. However, hints of efficacy from exploratory analyses support the idea that starting treatment earlier in the course of the disease might be more effective. A closer look at the failed trials will help de-risk future trials.

摘要

缺失主要疗效终点的试验引发了这样一个问题

是药物选择不当还是疾病生物学的局限性导致了失败。在一些试验中,药物似乎未达到足以产生临床益处的生化效应阈值。这表明需要研发在耐受剂量下更具活性的改良药物。在其他试验中,尚不清楚观察到的生物标志物变化与潜在疗效之间的关系。然而,探索性分析中显示的疗效线索支持了这样一种观点,即在疾病进程中更早开始治疗可能更有效。仔细研究失败的试验将有助于降低未来试验的风险。

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