AI Article Synopsis

  • In April 2018, Japan implemented the Clinical Trials Act to regulate investigator-initiated clinical trials, prompting a study to assess its impact on research activity.
  • Analysis of data from Tokushima University showed a decrease in new applications for clinical studies from pre-Act years (2015-2017) to post-Act years (2018-2019), indicating reduced interventional studies initiated.
  • The study suggests a need for further research to confirm this trend and explore methods, like involving more clinical research coordinators, to enhance clinical study engagement under the new regulations.

Article Abstract

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.

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http://dx.doi.org/10.1248/bpb.b21-00753DOI Listing

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