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减轻临床前学术药物研发中的风险。

Mitigating risk in academic preclinical drug discovery.

作者信息

Dahlin Jayme L, Inglese James, Walters Michael A

机构信息

Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic College of Medicine, Rochester, Minnesota 55905, USA.

1] National Center for Advancing Translational Sciences (NCATS), National Institutes of Health (NIH), Rockville, Maryland 20850, USA. [2] National Human Genome Research Institute, Bethesda, Maryland, 20892, USA.

出版信息

Nat Rev Drug Discov. 2015 Apr;14(4):279-94. doi: 10.1038/nrd4578.

Abstract

The number of academic drug discovery centres has grown considerably in recent years, providing new opportunities to couple the curiosity-driven research culture in academia with rigorous preclinical drug discovery practices used in industry. To fully realize the potential of these opportunities, it is important that academic researchers understand the risks inherent in preclinical drug discovery, and that translational research programmes are effectively organized and supported at an institutional level. In this article, we discuss strategies to mitigate risks in several key aspects of preclinical drug discovery at academic drug discovery centres, including organization, target selection, assay design, medicinal chemistry and preclinical pharmacology.

摘要

近年来,学术性药物研发中心的数量大幅增加,为将学术界基于好奇心的研究文化与行业中严格的临床前药物研发实践相结合提供了新机遇。为充分实现这些机遇的潜力,学术研究人员了解临床前药物研发中固有的风险,以及在机构层面有效组织和支持转化研究项目非常重要。在本文中,我们讨论了在学术性药物研发中心临床前药物研发的几个关键方面降低风险的策略,包括组织、靶点选择、分析方法设计、药物化学和临床前药理学。

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