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Interactions between Inter Partes Review and Hatch-Waxman Litigations

机译:当事人间审查与Hatch-Waxman诉讼之间的相互作用

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Generic drug development in the United States is governed by the Hatch-Waxman Act (HWA), which sets forth the “patent linkage” system requiring resolution of patent disputes before a generic drug can be approved for marketing. The emergence of Inter Partes Review (IPR), an effective administrative proceeding to weed out low-quality patents, is believed by some to have endangered the HWA balance between brand-name and generic drug makers. Here we describe an empirical analysis profiling the influences of IPR on patent linkage. Our results indicate that fewer than 10% of the HWA-litigated patents are subject to parallel IPR challenges. Importantly, IPR yields a slightly higher claim invalidation rate but a much lower settlement rate than court litigations, which may not benefit generic drug makers. Furthermore, IPR is employed by non-first generic drug makers, presumably to break into the market occupied by brand-name and the first generic makers. Overall, IPR seems not to play a dominant role, but to serve strategic functions in HWA disputes.
机译:在美国,仿制药的开发受《哈奇-瓦克斯曼法》(HWA)的约束,该法案提出了“专利联系”制度,要求在仿制药获准上市之前必须解决专利纠纷。部分人士认为,跨部门审查(IPR)的出现是一种有效的行政程序,可以清除低质量的专利,这已经危及了品牌和非专利药制造商之间的HWA平衡。在这里,我们描述了一个实证分析,剖析了知识产权对专利链接的影响。我们的结果表明,只有不到10%的HWA诉讼专利受到并行的IPR挑战。重要的是,与法院诉讼相比,知识产权产生的索赔无效率略高,但解决率却低得多,这可能不会使仿制药商受益。此外,非第一类非专利药物生产商采用了知识产权,大概是打入了由品牌和第一类非专利药物生产商占领的市场。总体而言,知识产权似乎并没有发挥主导作用,而是在HWA争端中发挥战略作用。

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