Feuerstein Giora Z, Zaleska Margaret M, Krams Michael, Wang Xinkang, Day Mark, Rutkowski Julia L, Finklestein Seth P, Pangalos Menelas N, Poole Michael, Stiles Gary L, Ruffolo Robert R, Walsh Frank L
Wyeth Research, Collegeville, Pennsylvania 19426, USA.
J Cereb Blood Flow Metab. 2008 Jan;28(1):217-9. doi: 10.1038/sj.jcbfm.9600516. Epub 2007 Jun 20.
The continued failure in approving new drugs for treatment of acute stroke has been recently set back by the failure of the NXY-059 (Stroke-Acute Ischemic NXY Treatment (SAINT) II) trial. The disappointment was heightened by the latter study being viewed as a most promising compound for stroke drug development program based on the preclinical data. Since the SAINT I/II development program included many of the STAIR (Stroke Therapy Academic Industry Round table) guidelines, yet have still failed to achieve the expected efficacy, there is a clear need to continue and analyze the path forward for stroke drug discovery. To this end, this review calls for a consortium approach including academia, government (FDA/NIH), and pharmaceutical industry partnerships to define this path. It is also imperative that more attention is given to the evolving discipline of Translational Medicine. A key issue in this respect is the need to devote more attention to the characteristics of the drug candidate nature-target interaction, and its relationship to pharmacodynamic treatment end points. It is equally important that efforts are spent to prove that phenotypic outcomes are linked to the purported mechanism of action of the compound. Development of technologies that allows a better assessment of these parameters, especially in in vivo models are paramount. Finally, rational patient selection and new outcome scales tailored in an adaptive design model must be evaluated.
近期,NXY - 059(急性缺血性卒中NXY治疗(SAINT)II)试验的失败使急性卒中治疗新药获批方面持续存在的失败状况雪上加霜。基于临床前数据,后一项研究被视为卒中药物研发项目中最具潜力的化合物,这使得失望情绪愈发强烈。由于SAINT I/II研发项目纳入了许多卒中治疗学术产业圆桌会议(STAIR)指南,但仍未达到预期疗效,显然有必要继续并分析卒中药物研发的前进道路。为此,本综述呼吁采取一种联合方法,包括学术界、政府(美国食品药品监督管理局/美国国立卫生研究院)和制药行业合作来确定这条道路。同样迫切的是,要更加关注转化医学这一不断发展的学科。在这方面的一个关键问题是,需要更加关注候选药物与靶点相互作用的特性及其与药效学治疗终点的关系。同样重要的是,要努力证明表型结果与化合物所谓的作用机制相关联。开发能够更好评估这些参数的技术至关重要,尤其是在体内模型中。最后,必须评估合理的患者选择以及在适应性设计模型中量身定制的新结局量表。