Fisher Marc, Albers Gregory W, Donnan Geoffrey A, Furlan Anthony J, Grotta James C, Kidwell Chelsea S, Sacco Ralph L, Wechsler Lawrence R
UMass/Memorial Healthcare Center, 119 Belmont St, Worcester, MA 01605, USA.
Stroke. 2005 Aug;36(8):1808-13. doi: 10.1161/01.STR.0000173403.60553.27. Epub 2005 Jul 14.
Previous Stroke Therapy Academic Industry Roundtable (STAIR) meetings focused on preclinical evidence of drug efficacy and enhancing acute stroke trial design and performance. A fourth (STAIR-IV) was held to discuss relevant issues related to acute stroke drug development and regulatory approval.
The STAIR-IV meeting had 3 main focus areas. The first topic was novel approaches to statistical design of acute stroke trials and appropriate outcome measures. The second focus was the need for better cooperation among participants in stroke therapy development that may be addressed through a national consortium of stroke trial centers in the United States and elsewhere. Lastly, regulatory issues related to the approval of novel mono and multiple acute stroke therapies were discussed.
The development of additional acute stroke therapies represents a large unmet need with many remaining challenges and also opportunities to incorporate novel approaches to clinical trial design that will lead to regulatory approval. The STAIR-IV meeting explored new concepts of trial methodology and data analysis, initiatives for implementing a US clinical trialist consortium, and pertinent regulatory issues to expedite approval of novel therapies.
既往的卒中治疗学术产业圆桌会议(STAIR)聚焦于药物疗效的临床前证据以及改善急性卒中试验的设计与实施。第四届会议(STAIR-IV)旨在讨论急性卒中药物研发及监管批准的相关问题。
STAIR-IV会议有3个主要重点领域。第一个主题是急性卒中试验统计设计的新方法及合适的结局指标。第二个重点是卒中治疗研发参与者之间加强合作的必要性,这可通过美国及其他地区的卒中试验中心全国性联盟来实现。最后,讨论了与新型单药及多种急性卒中疗法批准相关的监管问题。
更多急性卒中疗法的研发存在大量未满足的需求,仍有诸多挑战,但也有机会采用新型临床试验设计方法以获得监管批准。STAIR-IV会议探讨了试验方法和数据分析的新概念、建立美国临床试验专家联盟的举措以及加速新型疗法批准的相关监管问题。