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Matched analysis on orphan drug designations and approvals: cross regional analysis in the United States, the European Union, and Japan

机译:孤儿药名称和批准的匹配分析:美国,欧盟和日本的跨地区分析

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Orphan drugs have become a key area of focus in drug development for resolving unmet medical needs. The Orphan Drug Act in the USA and similar legislation in Japan, the European Union (EU), and several other countries has been enacted since 1983. This study provides a quantitative review of all orphan drug designations and approvals since the implementation of orphan drug legislation in key three regions. This study also identified and reviewed 'commonly designated' drugs across regions. Out of approximately 5000 designations, approximately 800 designations were common among the USA, EU, and/or Japan. Regional similarities, differences, and trends were identified. It is important to understand these aspects and the crucial role of orphan drug designation in global drug development.
机译:孤儿药物已成为解决未满足的医疗需求的药物开发的重点领域。自1983年以来,美国颁布了《孤儿药法案》,日本,欧盟(EU)和其他几个国家也颁布了类似的立法。这项研究对自实施孤儿药立法以来所有孤儿药的名称和批准进行了定量审查。在关键的三个地区。这项研究还确定并审查了跨地区的“通用”药物。在大约5000个指定中,美国,欧盟和/或日本共有大约800个指定。确定了区域的相似性,差异和趋势。重要的是要了解这些方面以及孤儿药名称在全球药物开发中的关键作用。

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