Department of Medicine, The Royal Melbourne Hospital, The University of Melbourne, Parkville, Victoria, Australia.
Epilepsia. 2013 Aug;54 Suppl 4:70-4. doi: 10.1111/epi.12300.
There is a pressing need to address the current major gaps in epilepsy treatment, in particular drug-resistant epilepsy, antiepileptogenic therapies, and comorbidities. A major concern in the development of new therapies is that current preclinical testing is not sufficiently predictive for clinical efficacy. Methodologic limitations of current preclinical paradigms may partly account for this discrepancy. Here we propose and discuss a strategy for implementing a "phase II" multicenter preclinical drug trial model based on clinical phase II/III studies designed to generate more rigorous preclinical data for efficacy. The goal is to improve the evidence resulting from preclinical studies for investigational new drugs that have shown strong promise in initial preclinical "phase I" studies. This should reduce the risk for expensive clinical studies in epilepsy and therefore increase the appeal for funders (industry and government) to invest in their clinical development.
目前迫切需要解决癫痫治疗方面的一些重大差距,特别是耐药性癫痫、抗癫痫发生治疗和合并症。在开发新疗法方面,一个主要关注点是目前的临床前测试对临床疗效的预测性不足。当前临床前范例的方法学限制可能部分解释了这种差异。在这里,我们提出并讨论了一种实施“二期”多中心临床前药物试验模型的策略,该模型基于旨在生成更严格的临床前疗效数据的临床二期/三期研究设计。目标是提高在初步临床“一期”研究中表现出良好前景的新型研究药物的临床前研究结果的证据质量。这应该降低癫痫昂贵的临床研究的风险,从而增加利益相关者(工业界和政府)投资其临床开发的吸引力。