Characteristics and outcomes of the drug patent linkage system in China

IF 5.9 2区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Globalization and Health Pub Date : 2024-04-15 DOI:10.1186/s12992-024-01035-x
Xue-Fang Yao
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Abstract

On July 4, 2021, China officially introduced the drug patent linkage system, which has made more localized adjustments than have similar systems in the US and South Korea. This study describes the characteristics and outcomes of China’s patent linkage system. For this study, we used the database of China’s patent information registration platform for marketed drugs to capture all listed patents and patent certifications from June 25, 2021, to June 30, 2023. We used descriptive statistics for the above data to assess the impact of patent linkage on branded drug manufacturers, generic drug manufacturers, and the public’s access to medicines. During the study period, the patents of 632 branded drugs were listed, and 5058 ANDAs submitted patent certifications to the Registration Platform. Of these 632 branded drugs, 462 (73.1%) drugs were approved before the year of patent registration, and the average number of listed patents per drug was 1.8, with a standard deviation of 1.4. However, of these 5058 ANDAs, P1 certifications accounted for 85.1%, and P3 and P4 certifications accounted for 16% combined. In addition, according to the detailed statistics of P2 certifications, we found that the proportion of patent invalidation cases was 46.4%. The remaining validity of the patents corresponding to P3 certifications was longer, with a median value of 17 months, and the IQR was 10-30.75, ranging from − 2 to 204 months. China’s patent linkage aims to promote the balance of multiple interests —innovation, imitation and public health—and has its own system characteristics. Patent listing and patent certification are the key indicators reflecting the implementation effect of the system. From the perspective of system outcomes, ANDAs have been connected to the patent linkage system in an orderly manner, but the growth of patent challenges is not obvious. Moreover, manufacturers of foreign branded drugs that have not yet entered the Chinese market need to pay more attention to the role of patent listing.
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中国药品专利链接制度的特点和成果
2021 年 7 月 4 日,中国正式引入药品专利链接制度,与美国和韩国的类似制度相比,中国对该制度进行了更多的本土化调整。本研究介绍了中国专利链接制度的特点和成果。在本研究中,我们使用了中国上市药品专利信息登记平台数据库,以获取 2021 年 6 月 25 日至 2023 年 6 月 30 日期间的所有上市专利和专利证书。我们对上述数据进行了描述性统计,以评估专利联动对品牌药生产企业、仿制药生产企业和公众用药的影响。在研究期间,共有 632 种品牌药的专利被列入,5058 个 ANDAs 向注册平台提交了专利认证。在这 632 种品牌药品中,有 462 种(73.1%)药品在专利注册当年之前获得批准,平均每种药品的上市专利数为 1.8,标准差为 1.4。然而,在这 5058 个 ANDA 中,P1 认证占 85.1%,P3 和 P4 认证合计占 16%。此外,根据对 P2 证书的详细统计,我们发现专利无效案件的比例为 46.4%。P3认证对应的专利剩余有效期较长,中位值为17个月,IQR为10-30.75,范围在-2-204个月之间。中国的专利联动旨在促进创新、模仿和公众健康等多方利益的平衡,具有自身的制度特点。专利上市和专利认证是反映制度实施效果的关键指标。从制度成果来看,ANDA 与专利链接制度的衔接有序,但专利挑战的增长并不明显。此外,尚未进入中国市场的国外品牌药品生产企业需要更加重视专利上市的作用。
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来源期刊
Globalization and Health
Globalization and Health PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH-
CiteScore
18.40
自引率
1.90%
发文量
93
期刊介绍: "Globalization and Health" is a pioneering transdisciplinary journal dedicated to situating public health and well-being within the dynamic forces of global development. The journal is committed to publishing high-quality, original research that explores the impact of globalization processes on global public health. This includes examining how globalization influences health systems and the social, economic, commercial, and political determinants of health. The journal welcomes contributions from various disciplines, including policy, health systems, political economy, international relations, and community perspectives. While single-country studies are accepted, they must emphasize global/globalization mechanisms and their relevance to global-level policy discourse and decision-making.
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