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A Design-Around Solution for a MMX-Based Tablet Drug Comprising Mesalazine-A Lesson from Shire Development, LLC v. Watson Pharmaceuticals, Inc.

机译:关于MSAlazine的基于MMX的片剂药物的一种设计解决方案 - 来自Shire Deviopment的课程,LLC v。Watson Pharmaceuticals,Inc。

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This article explores Shire Development, LLC v. Watson Pharmaceuticals, Inc., 848 F.3d 981 (Fed. Cir. 2017) and illustrates some implications for designing around a MMX-based tablet drug, Lialda. The MMX technology is known for its lipophilic matrix and hydrophilic matrix in a tablet, while the former matrix is dispersed within the latter one. In Shire Development, LLC, the disputed claim recited a Markush limitation for the hydrophilic matrix and excludes unlisted materials from the hydrophilic matrix. On the other hand, the accused generic drug included magnesium stearate, a lipophilic material, in its hydrophilic matrix and, therefore, did not infringe the disputed patent. The case opens a door for generic drug companies to design around the patented MMX technology underlying Lialda.
机译:本文探讨了Shire Development,LLC v.Watson Pharmaceuticals,Inc。,848 F.3D 981(Fapl。Cir。Cir。2017)并说明了对设计基于MMX的片剂药物,Lialda的一些影响。 MMX技术以其亲脂基质和亲水基质在片剂中已知,而前者基质分散在后者内。 在Shire Development中,LLC,有争议的权利要求叙述了亲水基质的标记限制,并排除了来自亲水基质的非上市材料。 另一方面,被控件通用药物包括硬脂酸镁,亲水材料,其亲水基质,因此没有侵犯争议的专利。 该案例为普通药物公司开辟了一扇门,以设计Lialda底层专利的MMX技术。

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