Biotechnology Discovery Research, Lilly Research Laboratories, Lead Generation , 355 E. Merrill St, Indianapolis, IN 46285 , USA +1 317 655 6783 ; +1 317 277 2934 ;
Expert Opin Drug Discov. 2014 Feb;9(2):115-8. doi: 10.1517/17460441.2014.870150. Epub 2013 Dec 12.
The pharmaceutical industry is confronted by increasing costs of clinical development and diminishing productivity. The most challenging aspect of drug development has been the failure of therapeutics in expensive Phase II or III trials, and this is most commonly due to lack of efficacy. More can be done during the drug discovery phase to optimize efficacy-testing in animal models by expending resources to explore the congruence of the animal model with the human disease. Historically, relatively little attention has been paid to validation of these models, but access to molecular mRNA and genetic profiling offers a new lens through which the similarity of these disease models to human diseases can be examined and their utility for exploring therapeutic efficacy can be optimized. Exploring congruent experimental end points in clinical and preclinical experiments will also increase confidence of success in late phase clinical development. The expense of this investment is trivial compared to the costs of a failed clinical trial, more than justifying this endeavor.
制药行业面临着临床开发成本的不断增加和生产力的不断下降。药物开发最具挑战性的方面一直是昂贵的 II 期或 III 期试验中治疗方法的失败,而这主要是由于缺乏疗效。在药物发现阶段,可以通过投入资源来探索动物模型与人类疾病的一致性,从而在优化动物模型的疗效测试方面做得更多。从历史上看,相对较少关注这些模型的验证,但获得分子 mRNA 和遗传分析为检查这些疾病模型与人类疾病的相似性以及优化其探索治疗效果的效用提供了一个新的视角。探索临床和临床前实验中一致的实验终点也将增加后期临床开发成功的信心。与临床试验失败的成本相比,这种投资的费用微不足道,完全可以证明这一努力是合理的。