Department of Regulatory Science, Faculty of Pharmacy, Meiji Pharmaceutical University, Tokyo, Japan.
Global Regulatory Science, Gifu Pharmaceutical University, Gifu, Japan.
Clin Pharmacol Ther. 2022 Oct;112(4):817-823. doi: 10.1002/cpt.2641. Epub 2022 Jun 7.
Compassionate use is a system that provides patients with exceptional access to investigational new drugs to treat life-threatening diseases that have no effective conventional treatments. The purpose of this study was to characterize and assess the current status of the compassionate use program's application in Japan by evaluating expanded access clinical trials (EACTs) conducted between 2016 and 2021. In this study, a data set containing all EACTs, and pivotal clinical trials (PCTs) conducted in Japan between February 2016 and April 2021 was obtained from the Pharmaceutical and Medical Devices Agency, systemically reviewed, and analyzed. During the 5 years since EACTs began in Japan, out of 2,031 PCTs, 31 EACTs were conducted in Japan. Twenty-four trials (77.4%) of the 31 EACTs used anticancer drugs and 5 of those trials (16.1%) were conducted in children. Furthermore, we conducted an EACT survey for drugs with a high degree of social and patient demands as recommended in the EACT notification. Among the 2,031 PCTs, we found 152 trials with high degree of social and patient demands. Of these, EACT was implemented in 17 trials (11.2%). Days from the start of the EACT to the submission of new drug applications and the approval were 9.0 (67.0-56.5) and 208.0 (172.8-308.8) days, respectively. Of the 31 EACTs conducted, 24 (77.4%) drugs have been approved as of August 2021. This first comprehensive study on EACTs clarified the current status and issues of Japan's compassionate use system and the 5 years since the program initiated.
同情用药是一种为患有危及生命且无有效常规治疗方法的疾病的患者提供特殊途径获得试验性新药的制度。本研究旨在通过评估 2016 年至 2021 年间进行的扩大准入临床试验(EACT)来描述和评估日本同情用药计划应用的现状。在这项研究中,从药品和医疗器械管理局获得了一个包含所有 EACT 和在日本进行的关键性临床试验(PCT)的数据集,对其进行了系统回顾和分析。自日本开展 EACT 以来的 5 年中,在 2031 项 PCT 中,有 31 项在日本开展了 EACT。在这 31 项 EACT 中,有 24 项(77.4%)试验使用了抗癌药物,其中 5 项(16.1%)试验在儿童中进行。此外,我们还按照 EACT 通知建议对具有高度社会和患者需求的药物进行了 EACT 调查。在 2031 项 PCT 中,我们发现有 152 项具有高度社会和患者需求的试验。在这些试验中,有 17 项(11.2%)实施了 EACT。从 EACT 开始到提交新药申请和批准的时间分别为 9.0(67.0-56.5)和 208.0(172.8-308.8)天。在已开展的 31 项 EACT 中,截至 2021 年 8 月,有 24 种(77.4%)药物已获得批准。这是第一项关于日本 EACT 的全面研究,阐明了日本同情用药制度的现状和问题,以及该计划启动 5 年来的情况。