Sarpatwari Ameet, Kesselheim Aaron S, Cook-Deegan Robert
Brigham and Women's Hospital/Harvard Medical School.
Arizona State University.
J Health Polit Policy Law. 2022 Dec 1;47(6):879-895. doi: 10.1215/03616878-10041247.
More than 40 years have passed since the enactment of the Patent and Trademark Amendment (Bayh-Dole) Act, which authorized institutions to patent inventions arising from federally funded research. Although some experts have heralded the Bayh-Dole Act as ushering in a new era of technological advances, others have been less sanguine about its impact. In recent years, the high price of prescription drugs and the patenting of COVID-19 therapeutics and vaccines developed with substantial federal government support have rekindled the debate over whether companies should receive more restricted rights to products originating with government funding. This article traces the history leading to the enactment of the Bayh-Dole Act and critically assesses its strengths and weaknesses as well as unresolved questions concerning its scope. Based on this analysis, the authors propose reforms to better align the Bayh-Dole Act with public values and health outcomes, including clarifying government-use rights, making it easier to invoke march-in rights for failure to meet health and safety needs, increasing transparency in how patents are licensed, and testing different approaches to foster the development and application of inventions.
自《专利与商标修正案》(《拜杜法案》)颁布以来,40多年过去了,该法案授权机构为联邦政府资助研究产生的发明申请专利。尽管一些专家宣称《拜杜法案》开创了技术进步的新时代,但另一些人对其影响则不那么乐观。近年来,处方药的高昂价格以及在联邦政府大力支持下开发的新冠治疗药物和疫苗的专利问题,重新引发了关于公司对政府资助产品应否获得更有限权利的争论。本文追溯了导致《拜杜法案》颁布的历史,并批判性地评估了其优缺点以及有关其范围的未解决问题。基于这一分析,作者们提出了一些改革建议,以使《拜杜法案》更好地与公共价值观和健康成果保持一致,包括明确政府使用权、简化因未能满足健康和安全需求而援引政府强制许可权的程序、提高专利许可方式的透明度,以及试验不同方法以促进发明的开发和应用。