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日本药物滞后与药物损失评估:参与全球III期肿瘤学试验

Evaluation of drug lag and drug loss in Japan: participation in global phase III oncology trials.

作者信息

Shiga Kaname, Shibata Taro, Miyata Toshio

机构信息

Cooperative Major in Advanced Biomedical Sciences, Joint Graduate School of Tokyo Women'S Medical University and Waseda University, Waseda University, 2-2 Wakamatsucho, Shinjuku, Tokyo, 162-8480, Japan.

Medical Affairs Division, Johnson & Johnson, Tokyo, Japan.

出版信息

Int J Clin Oncol. 2025 Apr 11. doi: 10.1007/s10147-025-02756-8.

Abstract

BACKGROUND

Despite efforts to mitigate drug lag, discrepancies in drug approval timelines persist between Japan and the US, and increase in unapproved drugs has become a significant challenge. This study aimed to evaluate potential drug lag and drug loss by assessing Japan's participation in global phase III multinational/multiregional clinical trials (MRCTs) targeted cancers.

METHODS

Phase III MRCTs of anticancer drugs initiated between 2008 and 2022 were collected. Information of participant countries, study sponsor, study design, and cancer type were collected and analyzed by logistic regression analysis to identify factors affected Japan's participation.

RESULTS

Of 999 phase III MRCTs, Japan's participation every 5 years increased over 15 years (2008-2012: 34.3%, 2013-2017: 51.6%, 2018-2022: 60.2%), while Japan's non-participation numbers did not change (2008-2012: 157, 2013-2017: 167, 2018-2022: 165). In the multivariate logistic regression analysis, the absence of an operational base in Japan and minor cancers were negatively associated with Japan's participation in phase III MRCTs. Japan's participation was also associated with some cancer organs and drug modalities.

CONCLUSION

Potential future drug lag and increases of unapproved drugs were expected to increase. Since the inclusion of Japan in MRCTs results in shorter or no approval lag, Japan should promote to make circumstances where small overseas companies can include Japan in MRCTs.

摘要

背景

尽管为缓解药物滞后问题做出了努力,但日本和美国在药物批准时间上仍存在差异,未批准药物的增加已成为一项重大挑战。本研究旨在通过评估日本参与针对癌症的全球III期多国/多地区临床试验(MRCT)的情况,来评估潜在的药物滞后和药物损失。

方法

收集了2008年至2022年间启动的抗癌药物III期MRCT。收集参与国家、研究申办方、研究设计和癌症类型等信息,并通过逻辑回归分析进行分析,以确定影响日本参与的因素。

结果

在999项III期MRCT中,日本每5年的参与率在15年里有所上升(2008 - 2012年:34.3%,2013 - 2017年:51.6%,2018 - 2022年:60.2%),而日本未参与的数量没有变化(2008 - 2012年:157项,2013 - 2017年:167项,2018 - 2022年:165项)。在多变量逻辑回归分析中,在日本没有运营基地以及罕见癌症与日本参与III期MRCT呈负相关。日本的参与还与某些癌症器官和药物类型有关。

结论

预计未来潜在的药物滞后和未批准药物的增加将会加剧。由于将日本纳入MRCT可缩短批准滞后时间或消除批准滞后,日本应推动创造条件,使海外小公司能够将日本纳入MRCT。

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