Pharmaceutical Pipeline Divestitures Study: Preliminary Results

Robin C. Feldman
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Abstract

In evaluating mergers between pharmaceutical companies, the FTC frequently requires divestiture of drug products that are in the pipeline — that is, they have yet to be approved by the FDA or brought to market. This study examines the effectiveness of such pipeline mergers to ask whether the drugs in the pipeline, indeed, have created effective competition. The results suggest that pipeline divestitures fail to provide an effective measure of competition. Our study found that only 20 of the 56 pharmaceutical products divested as pipeline products between 2008 and 2018 are actively marketed today (36%). In other words, these pipeline divestitures only made it to market 36% of the time, let alone creating the type of active competitive balance one might hope for. It is a disappointing result for a frequently used policy, and it suggests that competition agencies might wish to rethink pipeline mergers as effective antidote to market consolidation as well as to create a “second look” policy for mergers that have relied on this mechanism.
药物管道剥离研究:初步结果
在评估制药公司之间的合并时,联邦贸易委员会经常要求剥离正在生产中的药品,也就是说,这些药品尚未得到FDA的批准或推向市场。本研究考察了这种管道合并的有效性,以询问管道中的药物是否确实创造了有效的竞争。结果表明,管道剥离未能提供一种有效的竞争衡量标准。我们的研究发现,在2008年至2018年期间作为管道产品剥离的56种药品中,只有20种今天积极上市(36%)。换句话说,这些即将剥离的资产只有36%的时间进入市场,更不用说创造人们可能希望的那种积极的竞争平衡了。对于一项经常使用的政策来说,这是一个令人失望的结果,它表明,竞争机构可能希望重新考虑管道合并,将其作为市场整合的有效解药,并为依赖于这一机制的合并制定一项“重新审视”政策。
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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