Clinical Research Center for Developmental Therapeutics, Tokushima University Hospital.
Ethics Committee of Tokushima University Hospital, Tokushima University Hospital.
Biol Pharm Bull. 2022;45(3):374-377. doi: 10.1248/bpb.b21-00753.
In April 2018, the Clinical Trials Act pertaining to investigator-initiated clinical trials was passed in Japan. The purpose of this study was to investigate activity in investigator-initiated clinical studies before and after enforcement of the new Clinical Trials Act. This was done by analysing the records of the Ethics Committee of Tokushima University Hospital, which reviews studies based on the Japanese government's Ethical Guidelines for Medical and Health Research Involving Human Subjects prior to the Clinical Trials Act, and records of the Certified Review Board established at Tokushima University under the Clinical Trials Act in 2018. The number of new applications to these two review boards during fiscal years 2015-2017 (pre-Act) and fiscal years 2018 and 2019 (post-Act) were used as an indicator of activity in investigator-initiated clinical studies. The number of new applications to the Ethics Committee was 303, 261, 316, 303, and 249 in 2015, 2016, 2017, 2018, and 2019, respectively. The data show that the total number of new interventional studies decreased from 50.3 in average in 2015-2017 (pre-Act) to 42 in 2018 and 40 in 2019 (post-Act), respectively. These results suggest that fewer interventional studies were started following enforcement of the new Clinical Trials Act. To confirm this trend and identify contributing factors, further studies are required. In addition, possible way, such as broader contribution of clinical research coordinators, to promote clinical studies in the new Clinical Trials Act era should be examined.
2018 年 4 月,日本通过了与研究者发起的临床试验相关的《临床试验法》。本研究旨在调查该新法规实施前后研究者发起的临床试验的活跃度。本研究通过分析审查日本政府《涉及人体的医疗和健康研究伦理指南》的徳岛大学医院伦理委员会的记录,以及徳岛大学在 2018 年根据《临床试验法》设立的认证审查委员会的记录,来实现上述目的。在 2015-2017 财年(法规前)和 2018 财年和 2019 财年(法规后),将向这两个审查委员会提交的新申请数量作为研究者发起的临床试验活跃度的指标。伦理委员会的新申请数量在 2015 年、2016 年、2017 年、2018 年和 2019 年分别为 303、261、316、303 和 249。数据表明,新的介入性研究总数从 2015-2017 年(法规前)的平均 50.3 项减少到 2018 年的 42 项和 2019 年的 40 项。这些结果表明,新的《临床试验法》实施后,介入性研究的数量有所减少。为了确认这一趋势并确定促成因素,需要进一步研究。此外,应该检查在新的《临床试验法》时代促进临床研究的可能途径,例如更广泛地发挥临床研究协调员的作用。