一项案例研究,评估并购和许可对美国食品及药物管理局批准领先制药公司药品的影响。

IF 6.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Alexander Schuhmacher , Kyrylo Grinchenko , Oliver Gassmann , Dominik Hartl , Markus Hinder
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引用次数: 0

摘要

尽管最近FDA批准的新药有所增加,但领先的制药公司继续面临研发生产力的挑战。这突出表明需要更好地理解它们的研发概念和相关研发产出的背景。因此,我们对2012年至2021年间研发支出、研发强度、并购交易和许可协议对领先制药公司新药批准的影响进行了系统评估。我们的分析为区分研发因素提供了关键见解:虽然研发支出和并购交易数量与新药批准数量相关,但我们的分析显示与研发强度或许可协议数量无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A case study assessing the impact of M&A and licensing on FDA drug approvals of leading pharmaceutical companies
Despite a recent increase in FDA new drug approvals, leading pharmaceutical companies continue to face R&D productivity challenges. This highlights the need to better understand the context of their R&D concepts and related R&D outputs. Consequently, we conducted a systematic assessment of the impact of R&D expenditures, R&D intensities, mergers & acquisitions (M&A) deals and licensing agreements on new drug approvals of leading pharmaceutical companies between 2012 and 2021. Our analysis provides key insights into differentiating R&D factors: whereas R&D expenditures and the number of M&A deals correlate with the number of new drug approvals, our analysis shows no correlation with R&D intensity or the number of licensing agreements.
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来源期刊
Drug Discovery Today
Drug Discovery Today 医学-药学
CiteScore
14.80
自引率
2.70%
发文量
293
审稿时长
6 months
期刊介绍: Drug Discovery Today delivers informed and highly current reviews for the discovery community. The magazine addresses not only the rapid scientific developments in drug discovery associated technologies but also the management, commercial and regulatory issues that increasingly play a part in how R&D is planned, structured and executed. Features include comment by international experts, news and analysis of important developments, reviews of key scientific and strategic issues, overviews of recent progress in specific therapeutic areas and conference reports.
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