Developing Novel Drugs

Joshua L. Krieger, Danielle Li, D. Papanikolaou
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引用次数: 31

Abstract

We analyze the economic tradeoffs associated with firms' decisions to invest in incremental and radical innovation, in the context of pharmaceutical research and development. We develop a new, ex ante, measure of a drug candidate's innovativeness by comparing its chemical structure to that of previously developed drug candidates: this allows us to better distinguish between novel and so-called “me-too” drugs. We show that, on average, novel drug candidates 1) generate higher private and social returns conditional on approval (as measured by revenues, stock market returns, clinical value added, and patent citations) but 2) are riskier in that they are less likely to be approved by the FDA. Using variation in the expansion of Medicare prescription drug coverage, we show that firms respond to a plausibly exogenous positive shock to their net worth by developing more chemically novel drug candidates, as opposed to more “me-too” drugs. This pattern suggests that, on the margin, firms perceive novel drugs to be more valuable ex-ante investments, but that financial frictions may hinder their willingness to invest in these riskier candidates.
开发新药
在医药研发的背景下,我们分析了与企业决定投资于渐进式创新和突破性创新相关的经济权衡。我们通过将候选药物的化学结构与先前开发的候选药物的化学结构进行比较,开发了一种新的、事前的衡量候选药物的创新性的方法:这使我们能够更好地区分新型药物和所谓的“仿制”药物。我们表明,平均而言,新候选药物1)在获得批准的条件下产生更高的私人和社会回报(以收入、股票市场回报、临床附加值和专利引用来衡量),但2)风险更大,因为它们不太可能获得FDA的批准。利用医疗保险处方药覆盖范围扩大的变化,我们表明,企业通过开发更多化学上新颖的候选药物,而不是更多的“模仿”药物,来应对可能对其净资产产生的外源性积极冲击。这种模式表明,在边际上,公司认为新药是更有价值的事前投资,但财务摩擦可能会阻碍他们投资这些风险更高的候选药物的意愿。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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