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从Mayo v.Prometheus案看美国“专利适格标的”判断标准的变化 被引量:3

The Standard of Patentable Subject Matter after Mayo v. Prometheus Case
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摘要 就近期美国联邦最高法院Mayo v. Prometheus一案的判决,对美国《专利法》第101条"专利适格标的"产生的影响进行了研究。对Mayo基本案情进行介绍后,梳理了近年来美国《专利法》第101条专利适格标的范围及其检测标准的变化,指出美国专利标的物范围一直缺乏清晰、明确的界定;专利适格标的检测方法虽历经多次变革,但始终无法形成一个统一、清晰的检测标准。从法律功能、专利效力、产业发展等角度,分析了Mayo案件判决产生的影响,并就企业创新成果的保护、专利申请提出了建议。 This article provides analysis and insight on the U.S. Supreme Court's recent ruling in Mayo v. Prometheus involving patent eligibility of methods in the area of personalized medicine. A review of the recent doctrinal development is conducted after the Mayo case's introduction. The study shows that the standard of patentable subject matter under 35 U.S.C 101 suffers from a lack of clarity. Then, the article analyzes how Mayo v. Prometheus may affect the existing patents, the examination and decision implemented by the USPTO, and the developing of the life science area. Finally, some strategies and practices are provided to help the inventors to protect innovation in light of the Mayo's decision.
作者 漆苏 朱雪忠
出处 《知识产权》 CSSCI 北大核心 2012年第9期87-94,共8页 Intellectual Property
基金 教育部人文社会科学研究一般项目(项目编号:11YJA630224)资助 华中科技大学博士生论文创新基金项目资助
关键词 MAYO PROMETHEUS 专利适格标的 检测方法 演进 建议 Mayo Prometheus patentable subject matter test method evolution suggestion
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参考文献24

  • 1Mayo Collaborative Service v. Prometheus Laboratories Inc., 132 S. Ct. 1289, 101 USPQ 2d 1961 (2012).
  • 2Diamond v. Diehr, 450 U.S. 175 (1981).
  • 3Bilski v. Kappos, 130 S. Ct. 3218, 95 USPQ2d 1001 (2010).
  • 4Mayo Collaborative Service v. Prometheus Laboratories Inc, 628 F.3d 1347, 97 USPQ 2d 1097 (Fed. Cir 2010).
  • 5Prometheus Labs., Inc. v. Mayo Collaborative Servs. & Mayo Clinic Rochester, 628 F.3d 1347 (Fed. Cir., 2010).
  • 635. U.S.C 101 (2011).
  • 7《欧洲专利公约》第52条.
  • 8U.S. Const. art. VIII, 8.
  • 9Henry O' Reilly v. Samuel F. B. Morse, 56 U.S. 62 (1854).
  • 10American Fnlit Growers v. Brodgex, 283 U.S. 1, 11 (1931).

同被引文献22

  • 1陈朝晖,郑洪.从美国专利文献看中药复方在国际上的专利保护方式[J].中成药,2006,28(1):102-105. 被引量:9
  • 2杨莉,李野,董丽.美国药品专利保护研究及启示[J].中国新药杂志,2006,15(17):1425-1428. 被引量:7
  • 3Jennifer Vogel.Patenting DNA:Balancing the Need to Incentivize Innovation in Biotechnology with the Need to Make High-Quality Genetic Testing Accessible to Patients[J].Kansas Law Review,2012(61):257-293.
  • 4Joseph S.Classe.Genes and the Supremes:Will the Supreme Court Uphold Patents for Isolated Gene Se-quences? [J].Texas Tech Law Review,2013(45):533-564.
  • 5Sethr Ogden.The Federal Circuit's Decision In Myri-ad.Isolated DNA Molecules Are Patentable Subject Matter[J].American University Law Review,2011(2):442-455.
  • 6Richard Marsh.The Defendants:An Interview with Richard Marsh of Myriad Genetics[EB/OL].(2010-10-12)[2010-10-26].GENEWATCH,Oct.htp://is-suu.com/genewatchmagazine/docs/genewatch23-5.
  • 7Carl Shapiro.Navigating the Patent Thicket:Cross Li-censes,PatentPools,and Standard-setting [M]//A dam B Jaffe.Innovation Policy and the Economy Vo-hune 1.Massachusetts:MIT Press,2001:119-150.
  • 8Chris Holman,Will Gene Patents Impede Whole Ge-nome Sequencing?Deconstructing the Myth that 20% ofthe Human Genome is Patented[EB/OL].(2013-08-05)[2013-11-15].Holman's Biotech IP Blog,Aug.http://holmansbiotechipblog,blogspot,com/2011/08/will-gene-patents-impede-whole-genome.Html.
  • 9Donna M.Gitter.International Conflicts over Paten-ting Human DNA Sequences in the United States and the European Union An Argument for Compulsory Licensing and a Fair-Use Exemption [J].New York Univercity Law Review,2001(6):1623-1679.
  • 10Hu Y,Scherngell T,Man SN,et al.Is the United States still dominant in the global pharmaceutical innovation network[J].PLo S one,2013,8(11):e77 247.

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