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Cases Update: International roundup of recently filed cases and noteworthy rulings

机译:案件更新:国际上最近提交的案件和值得注意的裁决的综述

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In this ruling, the Federal Circuit affirmed the US Patent and Trademark Office's (USPTO's) decision that Pfizer was entitled to an earlier priority date for a claim to cDNA encoding the IL-13 receptor protein. The Board agreed with Pfizer that the question is "who first had in hand the actual isolated DNA of the count and appreciated its IL-13 bc function", not "the date each party first knew the complete sequence" of nu-cleotides as argued by Sanofi-Aventis. Sanofi was awarded priority with its December 6,1995 priority date because Pfizer's filing date was March 1,1996. Pfizer presented evidence that it had isolated and identified the cDNA before Sanofi's priority date, but not the complete sequence because of sequencing errors. The Board concluded that Pfizer had "the claimed polynucleotide in hand with some additional identifying information including at least a partial sequence',''and that Pfizer "established conception and actual reduction to practice of a polynucleotide within the scope of count 3" before Sanofi's priority date. Sanofi argued that until Pfizer had the correct sequence, "neither conception nor reduction to practice could occur." Pfizer argued that errors such as these were "routinely detected and corrected" and were actually corrected by December 12, 1995. The Federal Circuit panel affirmed the Board s decision.
机译:在该裁决中,联邦巡回法院确认了美国专利商标局(USPTO)的决定,即辉瑞有权对编码IL-13受体蛋白的cDNA要求更早的优先权。董事会同意辉瑞公司的观点,问题是“谁首先掌握了该计数的实际分离的DNA并赞赏其IL-13 bc功能”,而不是争论的“各方首先知道完整序列的日期”由Sanofi-Aventis。赛诺菲于1995年12月6日获得优先权,因为辉瑞公司的申请日为1996年3月1日。辉瑞公司提供的证据表明,它已在赛诺菲的优先权日之前分离并鉴定了cDNA,但由于测序错误,尚未分离出完整的序列。董事会的结论是,辉瑞公司“拥有要求保护的多核苷酸并带有一些至少包括部分序列的其他识别信息”,并且辉瑞公司“在赛诺菲制药公司成立之前确定并实际减少了在计数3范围内实施多核苷酸的工作”。赛诺菲(Sanofi)辩称,在辉瑞(Pfizer)拥有正确的顺序之前,“概念和实践的减少都不会发生。”辉瑞(Pfizer)辩称,“常规检测和纠正”这类错误,并在1995年12月12日之前得到了纠正。巡回小组确认了董事会的决定。

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