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阿斯利康五维框架对研发生产力的影响。

Impact of a five-dimensional framework on R&D productivity at AstraZeneca.

机构信息

Drug Safety and Metabolism, IMED Biotech Unit, AstraZeneca, 1 Francis Crick Avenue, Cambridge CB2 0RE, UK.

Discovery Sciences, IMED Biotech Unit, AstraZeneca, 35 Gatehouse Drive, Waltham, Massachusetts 02451, USA.

出版信息

Nat Rev Drug Discov. 2018 Mar;17(3):167-181. doi: 10.1038/nrd.2017.244. Epub 2018 Jan 19.

Abstract

In 2011, AstraZeneca embarked on a major revision of its research and development (R&D) strategy with the aim of improving R&D productivity, which was below industry averages in 2005-2010. A cornerstone of the revised strategy was to focus decision-making on five technical determinants (the right target, right tissue, right safety, right patient and right commercial potential). In this article, we describe the progress made using this '5R framework' in the hope that our experience could be useful to other companies tackling R&D productivity issues. We focus on the evolution of our approach to target validation, hit and lead optimization, pharmacokinetic/pharmacodynamic modelling and drug safety testing, which have helped improve the quality of candidate drug nomination, as well as the development of the right culture, where 'truth seeking' is encouraged by more rigorous and quantitative decision-making. We also discuss where the approach has failed and the lessons learned. Overall, the continued evolution and application of the 5R framework are beginning to have an impact, with success rates from candidate drug nomination to phase III completion improving from 4% in 2005-2010 to 19% in 2012-2016.

摘要

2011 年,阿斯利康启动了一项重大的研发(R&D)战略修订,旨在提高研发生产力,而 2005-2010 年期间,阿斯利康的研发生产力低于行业平均水平。修订战略的基石是将决策集中在五个技术决定因素(正确的目标、正确的组织、正确的安全性、正确的患者和正确的商业潜力)上。在本文中,我们描述了使用这种“5R 框架”取得的进展,希望我们的经验对其他解决研发生产力问题的公司有所帮助。我们专注于目标验证、命中和先导优化、药代动力学/药效学建模和药物安全测试方法的演变,这些方法有助于提高候选药物提名的质量,以及培养正确的文化,即通过更严格和定量的决策来鼓励“寻求真相”。我们还讨论了方法失败的地方和吸取的教训。总体而言,5R 框架的持续发展和应用开始产生影响,从候选药物提名到第三阶段完成的成功率从 2005-2010 年的 4%提高到 2012-2016 年的 19%。

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