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PhRMA 药物基因组学和药效动力学评估调查:下一步是什么?

PhRMA survey of pharmacogenomic and pharmacodynamic evaluations: what next?

机构信息

Department of Pharmacogenomics, Johnson & Johnson Pharmaceutical Research and Development, Raritan, New Jersey, USA.

出版信息

Clin Pharmacol Ther. 2012 Jun;91(6):1035-43. doi: 10.1038/clpt.2011.334.

Abstract

Interindividual variation in pharmacodynamic (PD) response to drugs is an ongoing area of research for drugs in clinical development, pre- and postapproval. To characterize how pharmacogenomic (PG ) variations can serves a predictor of differences in PD outcomes, the pharmaceutical industry has incorporated PG /PD analysis into clinical drug development. The Pharmaceutical Research and Manufacturers of America (PhRMA ) and the Industry Pharmacogenomics Working Group (I-PWG) conducted a survey of 16 pharmaceutical companies to ascertain to what extent PG/PD research is being incorporated into drug development. The survey results showed that, while the industry has made some attempt to incorporate PG/PD studies into drug development, application has been inconsistent. Nevertheless, several valid PG/PD markers have since emerged in drug labels. The I-PWG considers PG/PD research an important approach to improving success rates in drug development. This article reports the results of the survey and proposes steps toward increasing the use of PG/PD research by the industry.

摘要

药物药效学(PD)反应的个体间差异是临床开发、上市前和上市后药物研究的一个持续领域。为了描述药物基因组学(PG)变异如何作为 PD 结果差异的预测指标,制药行业已经将 PG/PD 分析纳入临床药物开发中。美国制药研究与制造商协会(PhRMA)和行业药物基因组学工作组(I-PWG)对 16 家制药公司进行了调查,以确定 PG/PD 研究在药物开发中被纳入的程度。调查结果表明,虽然该行业已经在将 PG/PD 研究纳入药物开发方面进行了一些尝试,但应用并不一致。尽管如此,一些有效的 PG/PD 标志物已经出现在药物标签中。I-PWG 认为 PG/PD 研究是提高药物开发成功率的重要方法。本文报告了调查结果,并提出了增加行业使用 PG/PD 研究的步骤。

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