Trends in Investigator-Initiated Clinical Studies at a University Hospital after Enforcement of the 2018 Clinical Trials Act in Japan
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 th...
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| Published in | Biological & pharmaceutical bulletin Vol. 45; no. 3; pp. 374 - 377 |
|---|---|
| Main Authors | , , , , , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Japan
The Pharmaceutical Society of Japan
01.03.2022
Japan Science and Technology Agency |
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| Online Access | Get full text |
| ISSN | 0918-6158 1347-5215 1347-5215 |
| DOI | 10.1248/bpb.b21-00753 |
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| 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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| AbstractList | 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. 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.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. |
| ArticleNumber | b21-00753 |
| Author | Hashimoto, Ichiro Takechi, Kenshi Sato, Yasutaka Hamano, Hirofumi Sakaguchi, Satoshi Nokihara, Hiroshi Chuma, Masayuki Kane, Chikako Yanagawa, Hiroaki Yagi, Kenta Kubo, Yoshiaki Goda, Mitsuhiro Aoe, Yuki |
| Author_xml | – sequence: 1 fullname: Goda, Mitsuhiro organization: Clinical Research Center for Developmental Therapeutics, Tokushima University Hospital – sequence: 1 fullname: Kane, Chikako organization: Clinical Research Center for Developmental Therapeutics, Tokushima University Hospital – sequence: 1 fullname: Kubo, Yoshiaki organization: Ethics Committee of Tokushima University Hospital, Tokushima University Hospital – sequence: 1 fullname: Nokihara, Hiroshi organization: Clinical Research Center for Developmental Therapeutics, Tokushima University Hospital – sequence: 1 fullname: Hashimoto, Ichiro organization: Certified Review Board of Tokushima University, Tokushima University – sequence: 1 fullname: Yagi, Kenta organization: Clinical Research Center for Developmental Therapeutics, Tokushima University Hospital – sequence: 1 fullname: Sato, Yasutaka organization: Clinical Research Center for Developmental Therapeutics, Tokushima University Hospital – sequence: 1 fullname: Sakaguchi, Satoshi organization: Clinical Research Center for Developmental Therapeutics, Tokushima University Hospital – sequence: 1 fullname: Hamano, Hirofumi organization: Clinical Research Center for Developmental Therapeutics, Tokushima University Hospital – sequence: 1 fullname: Chuma, Masayuki organization: Clinical Research Center for Developmental Therapeutics, Tokushima University Hospital – sequence: 1 fullname: Takechi, Kenshi organization: Clinical Research Center for Developmental Therapeutics, Tokushima University Hospital – sequence: 1 fullname: Yanagawa, Hiroaki organization: Clinical Research Center for Developmental Therapeutics, Tokushima University Hospital – sequence: 1 fullname: Aoe, Yuki organization: Clinical Research Center for Developmental Therapeutics, Tokushima University Hospital |
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| Cites_doi | 10.2152/jmi.62.114 10.1126/science.341.6143.223 10.1248/bpb.b19-00929 10.1016/j.clinthera.2018.10.010 10.1093/jjco/hyaa028 10.2152/jmi.68.71 10.1177/2168479014522044 10.1186/1471-2288-11-148 10.14740/jocmr3602w 10.3109/10601333.2014.956932 10.3999/jscpt.51.255 |
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| References | 1) Yanagawa H. Current regulatory systems for clinical trials in Japan: still room for improvement. Clin. Res. Regul. Aff., 31, 25–28 (2014). 2) Urushihara H, Kawakami K. Academic clinical trials and drug regulations in japan: impacts of introducing the investigational new drug system. Ther. Innov. Regul. Sci., 48, 463–472 (2014). 13) Yanagawa H, Nokihara H, Yokoi H, Houchi H, Nagai M, Yamashita R, Suganuma N, Hyodo M. Present status and perspectives on future roles of Japanese clinical research coordinators. J. Clin. Med. Res., 10, 877–882 (2018). 3) Yanagawa H, Katashima R, Takeda N. Research ethics committees in Japan: a perspective from thirty years of experience at Tokushima University. J. Med. Invest., 62, 114–118 (2015). 15) Ohshima H, Aoyagi M, Tajima M, Nishimura S, Nomura T, Kato Y, Koike R, Suzuki Y, Yamashita S, Ikeda T, Aoki H, Kondo M. Considering the future of clinical research at the turning point of implementation of the new legislation in Japan—impact of the Clinical Trials Act on pharmaceutical industries; based on the results from the internal survey in JPMA. Clin. Eval., 47, 115–125 (2019). 10) Nakamura K, Shibata T. Regulatory changes after the enforcement of the new Clinical Trials Act in Japan. Jpn. J. Clin. Oncol., 50, 399–404 (2020). 11) Chuma M, Takechi K, Yagi K, Sakaguchi S, Nokihara H, Kane C, Sato Y, Niimura T, Goda M, Zamami Y, Ishizawa K, Yanagawa H. Academic investigators’ interest in promoting specified clinical trials: questionnaire survey before and after implementation of the Clinical Trial Act. J. Med. Invest., 68, 71–75 (2021). 12) Kaneko S, Nagashima T. Drug repositioning and target finding based on clinical evidence. Biol. Pharm. Bull., 43, 362–365 (2020). 7) Sawata H, Tsutani K. Funding and infrastructure among large-scale clinical trials examining cardiovascular diseases in Japan: evidence from a questionnaire survey. BMC Med. Res. Methodol., 11, 148 (2011). 8) Ministry of Health, Labour and Welfare. “The minutes of the Clinical Research Committee, Health Sciences Council, Ministry of Health, Labour and Welfare (31 August, 2017).”: ‹https://www.mhlw.go.jp/stf/shingi2/0000179030.html›, accessed 29 November, 2021. 6) Ministry of Health. Labour and Welfare. “Clinical Trials Act (Act No. 16 of 14 April 2017).”: ‹https://www.mhlw.go.jp/file/06-Seisakujouhou-10800000-Iseikyoku/0000163413.pdf›, accessed 29 November, 2021. 4) Normile D. Tampered data cast shadow on drug trial. Science, 341, 223 (2013). 5) Ministry of Health. Labour and Welfare. “Ethical guidelines for medical and health research involving human subjects.”: ‹https://www.mhlw.go.jp/content/10600000/000757206.pdf›, accessed 29 November, 2021. 14) Tsuruya N, Kawashima T, Shiozuka M, Nakanishi Y, Sugiyama D. Academia-industry cooperation in the medical field: matching opportunities in Japan. Clin. Ther., 40, 1807–1812 (2018). 9) Ozaki M, Harada Y, Toya W, Yamashita N, Fuse N, Sato A, Tsuboi M. A Survey of certified review boards under the Clinical Trials Act. Jpn. J. Clin. Pharmacol. Ther., 51, 255–265 (2020). 11 12 13 14 15 1 2 3 4 5 6 7 8 9 10 |
| References_xml | – reference: 10) Nakamura K, Shibata T. Regulatory changes after the enforcement of the new Clinical Trials Act in Japan. Jpn. J. Clin. Oncol., 50, 399–404 (2020). – reference: 12) Kaneko S, Nagashima T. Drug repositioning and target finding based on clinical evidence. Biol. Pharm. Bull., 43, 362–365 (2020). – reference: 15) Ohshima H, Aoyagi M, Tajima M, Nishimura S, Nomura T, Kato Y, Koike R, Suzuki Y, Yamashita S, Ikeda T, Aoki H, Kondo M. Considering the future of clinical research at the turning point of implementation of the new legislation in Japan—impact of the Clinical Trials Act on pharmaceutical industries; based on the results from the internal survey in JPMA. Clin. Eval., 47, 115–125 (2019). – reference: 9) Ozaki M, Harada Y, Toya W, Yamashita N, Fuse N, Sato A, Tsuboi M. A Survey of certified review boards under the Clinical Trials Act. Jpn. J. Clin. Pharmacol. Ther., 51, 255–265 (2020). – reference: 5) Ministry of Health. Labour and Welfare. “Ethical guidelines for medical and health research involving human subjects.”: ‹https://www.mhlw.go.jp/content/10600000/000757206.pdf›, accessed 29 November, 2021. – reference: 3) Yanagawa H, Katashima R, Takeda N. Research ethics committees in Japan: a perspective from thirty years of experience at Tokushima University. J. Med. Invest., 62, 114–118 (2015). – reference: 14) Tsuruya N, Kawashima T, Shiozuka M, Nakanishi Y, Sugiyama D. Academia-industry cooperation in the medical field: matching opportunities in Japan. Clin. Ther., 40, 1807–1812 (2018). – reference: 4) Normile D. Tampered data cast shadow on drug trial. Science, 341, 223 (2013). – reference: 1) Yanagawa H. Current regulatory systems for clinical trials in Japan: still room for improvement. Clin. Res. Regul. Aff., 31, 25–28 (2014). – reference: 8) Ministry of Health, Labour and Welfare. “The minutes of the Clinical Research Committee, Health Sciences Council, Ministry of Health, Labour and Welfare (31 August, 2017).”: ‹https://www.mhlw.go.jp/stf/shingi2/0000179030.html›, accessed 29 November, 2021. – reference: 2) Urushihara H, Kawakami K. Academic clinical trials and drug regulations in japan: impacts of introducing the investigational new drug system. Ther. Innov. Regul. Sci., 48, 463–472 (2014). – reference: 7) Sawata H, Tsutani K. Funding and infrastructure among large-scale clinical trials examining cardiovascular diseases in Japan: evidence from a questionnaire survey. BMC Med. Res. Methodol., 11, 148 (2011). – reference: 11) Chuma M, Takechi K, Yagi K, Sakaguchi S, Nokihara H, Kane C, Sato Y, Niimura T, Goda M, Zamami Y, Ishizawa K, Yanagawa H. Academic investigators’ interest in promoting specified clinical trials: questionnaire survey before and after implementation of the Clinical Trial Act. J. Med. Invest., 68, 71–75 (2021). – reference: 6) Ministry of Health. Labour and Welfare. “Clinical Trials Act (Act No. 16 of 14 April 2017).”: ‹https://www.mhlw.go.jp/file/06-Seisakujouhou-10800000-Iseikyoku/0000163413.pdf›, accessed 29 November, 2021. – reference: 13) Yanagawa H, Nokihara H, Yokoi H, Houchi H, Nagai M, Yamashita R, Suganuma N, Hyodo M. Present status and perspectives on future roles of Japanese clinical research coordinators. J. Clin. Med. Res., 10, 877–882 (2018). – ident: 3 doi: 10.2152/jmi.62.114 – ident: 4 doi: 10.1126/science.341.6143.223 – ident: 5 – ident: 12 doi: 10.1248/bpb.b19-00929 – ident: 14 doi: 10.1016/j.clinthera.2018.10.010 – ident: 10 doi: 10.1093/jjco/hyaa028 – ident: 11 doi: 10.2152/jmi.68.71 – ident: 2 doi: 10.1177/2168479014522044 – ident: 7 doi: 10.1186/1471-2288-11-148 – ident: 13 doi: 10.14740/jocmr3602w – ident: 15 – ident: 1 doi: 10.3109/10601333.2014.956932 – ident: 6 – ident: 9 doi: 10.3999/jscpt.51.255 – ident: 8 |
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| SubjectTerms | clinical research Clinical trials Clinical Trials Act Clinical Trials as Topic - legislation & jurisprudence Enforcement Hospitals, University Humans investigator Japan trend |
| Title | Trends in Investigator-Initiated Clinical Studies at a University Hospital after Enforcement of the 2018 Clinical Trials Act in Japan |
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