Gold Michael
Global Product Development, Neuroscience, PPD, Morrisville, NC, USA.
Alzheimers Dement (N Y). 2017 May 17;3(3):402-409. doi: 10.1016/j.trci.2017.04.005. eCollection 2017 Sep.
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.
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。