Global Clinical Pharmacology, Pfizer, Sandwich, UK.
Clin Pharmacol Ther. 2013 Jun;93(6):502-14. doi: 10.1038/clpt.2013.54. Epub 2013 Mar 14.
The pharmaceutical industry continues to face significant challenges. Very few compounds that enter development reach the marketplace, and the investment required for each success can surpass $1.8 billion. Despite attempts to improve efficiency and increase productivity, total investment continues to rise whereas the output of new medicines declines. With costs increasing exponentially through each development phase, it is failure in phase II and phase III that is most wasteful. In today's development paradigm, late-stage failure is principally a result of insufficient efficacy. This is manifested as either a failure to differentiate sufficiently from placebo (shown for both novel and precedented mechanisms) or a failure to demonstrate sufficient differentiation from existing compounds. Set in this context, this article will discuss the role model-based drug development (MBDD) approaches can and do play in accelerating and optimizing compound development strategies through a series of illustrative examples.
制药行业继续面临重大挑战。进入开发阶段的化合物很少能进入市场,每个成功所需的投资可能超过 18 亿美元。尽管尝试提高效率和增加生产力,但总投资持续上升,而新药的产量却在下降。随着每个开发阶段的成本呈指数级增长,失败的主要原因是 II 期和 III 期临床试验效果不足。在当今的开发模式下,晚期失败主要是由于疗效不足。这表现为与安慰剂的区分度不足(新型和传统机制都有这种情况),或者未能充分显示与现有化合物的区别。在此背景下,本文将通过一系列实例,讨论基于模型的药物开发(MBDD)方法在加速和优化化合物开发策略方面可以发挥的作用。