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一项关于日本和美国抗癌药物首次人体试验及获批概率的横断面研究。

A cross-sectional study on the first-in-human trials of anticancer drugs in Japan and the United States and the probability of approval.

作者信息

Mukaida Akari, Maeda Hideki

机构信息

Regulatory Science, Faculty of Pharmacy, Meiji Pharmaceutical University, 2-522-1, Noshio, Kiyose-City, Tokyo, 204-5255, Japan.

出版信息

Int J Clin Oncol. 2025 Aug 6. doi: 10.1007/s10147-025-02849-4.

DOI:10.1007/s10147-025-02849-4
PMID:40768014
Abstract

BACKGROUND

This study aimed to examine the characteristics of First-in-human (FIH) trials conducted in Japan and the US and whether the probability of approval for pharmaceuticals that had undergone FIH trials differs in the two countries.

METHODS

FIH trials of anticancer drugs initiated between 2007 and 2017 were investigated in this study. The trials were searched using ClinicalTrials.gov.

RESULTS

There were 22 FIH trials conducted in Japan and 261 in the US. Of these, six drugs (27.2%) were approved in Japan and 27 (10.3%) were approved in the US, indicating that the probability of approval was significantly higher for FIH trials conducted in Japan than in the US. Comparison of the characteristics of FIH trials between Japan and the US, showed that 81.8% of the FIH trials conducted in Japan were sponsored by the top 20 pharmaceutical companies, whereas 55.6% in the US were sponsored by non-top 20 companies (P = 0.003, Chi-square test). The number of patients was higher in Japan than in the US (P = 0.044). Further, all of the trials conducted in Japan were multiregional clinical trials in collaboration with other countries such as Europe and the US, whereas 49.0% of the trials in the US were conducted in the US alone (P < 0.001).

CONCLUSION

We inferred that the FIH trials conducted in Japan are multiregional clinical trials by major pharmaceutical companies with Europe and the US, and are conducted with drugs that are expected to have a high probability of successful approval.

摘要

背景

本研究旨在考察在日本和美国开展的首次人体试验(FIH)的特点,以及在这两个国家中,经过FIH试验的药物获批概率是否存在差异。

方法

本研究调查了2007年至2017年间启动的抗癌药物的FIH试验。通过ClinicalTrials.gov对这些试验进行检索。

结果

在日本开展了22项FIH试验,在美国开展了261项。其中,6种药物(27.2%)在日本获批,27种(10.3%)在美国获批,这表明在日本开展的FIH试验的获批概率显著高于美国。日本和美国FIH试验特点的比较显示,在日本开展的FIH试验中,81.8%由排名前20的制药公司赞助,而在美国这一比例为55.6%,由非排名前20的公司赞助(P = 0.003,卡方检验)。日本的患者数量多于美国(P = 0.044)。此外,在日本开展的所有试验都是与欧洲和美国等其他国家合作的多区域临床试验,而在美国,49.0%的试验仅在美国境内开展(P < 0.001)。

结论

我们推断,在日本开展的FIH试验是由大型制药公司与欧洲和美国合作进行的多区域临床试验,并且所试验的药物有望获得较高的获批成功率。

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本文引用的文献

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Ther Innov Regul Sci. 2025 Apr 8. doi: 10.1007/s43441-025-00771-5.
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Benchmarking R&D success rates of leading pharmaceutical companies: an empirical analysis of FDA approvals (2006-2022).领先制药公司研发成功率的基准分析:对美国食品药品监督管理局(FDA)2006年至2022年批准情况的实证分析
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J Comput Aided Mol Des. 2024 Aug 20;38(1):30. doi: 10.1007/s10822-024-00569-x.
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Trends in oncology drug lags in Japan from 2001 to 2020: A cross-sectional study.2001 年至 2020 年日本肿瘤药物研发滞后趋势:一项横断面研究。
Clin Transl Sci. 2023 Dec;16(12):2665-2674. doi: 10.1111/cts.13660. Epub 2023 Oct 17.
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