Doggrell Sheila A
Expert Opin Pharmacother. 2008 Apr;9(6):875-8. doi: 10.1517/14656566.9.6.875.
Torcetrapib was spectacularly withdrawn in December 2006, when a Phase III clinical trial showed increased cardiovascular adverse events.
To consider possible reasons why the development of torcetrapib proceeded so far before adverse events became apparent.
Published preclinical and clinical data for torcetrapib are reviewed.
RESULTS/CONCLUSIONS: It seems likely that independent preclinical testing would have shown that torcetrapib increased blood pressure. Such a finding might have halted the development of torcetrapib prior to clinical trial. Although the early clinical testing of torcetrapib showed favourable effects on the surrogate endpoints, an ability to increase blood pressure started to become apparent. When clinical outcome studies were undertaken with torcetrapib, it was shown not to have any benefit on atherosclerosis and to increase cardiovascular events. These finding might have come to light earlier if clinical outcomes studies had had a higher priority than repeated trials, in different populations, of torcetrapib on surrogate outcomes.
托彻普贝(torcetrapib)于2006年12月被惊人地撤回,当时一项III期临床试验显示心血管不良事件增加。
探讨托彻普贝在不良事件显现之前为何能发展到如此程度的可能原因。
回顾已发表的托彻普贝临床前和临床数据。
结果/结论:独立的临床前测试似乎有可能显示托彻普贝会升高血压。这样的发现可能会在临床试验之前停止托彻普贝的研发。尽管托彻普贝的早期临床试验显示对替代终点有有利影响,但升高血压的能力开始变得明显。当对托彻普贝进行临床结局研究时,结果显示它对动脉粥样硬化没有任何益处,反而会增加心血管事件。如果临床结局研究比在不同人群中对托彻普贝替代结局进行的重复试验具有更高的优先级,这些发现可能会更早地被揭示出来。