Recent trends for drug lag in clinical development of oncology drugs in Japan: does the oncology drug lag still exist in Japan?

Verfasser / Beitragende:
[Hideki Maeda, Tatsuo Kurokawa]
Ort, Verlag, Jahr:
2015
Enthalten in:
International Journal of Clinical Oncology, 20/6(2015-12-01), 1072-1080
Format:
Artikel (online)
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024 7 0 |a 10.1007/s10147-015-0825-4  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s10147-015-0825-4 
245 0 0 |a Recent trends for drug lag in clinical development of oncology drugs in Japan: does the oncology drug lag still exist in Japan?  |h [Elektronische Daten]  |c [Hideki Maeda, Tatsuo Kurokawa] 
520 3 |a Background: This study exhaustively and historically investigated the status of drug lag for oncology drugs approved in Japan. Methods: We comprehensively investigated oncology drugs approved in Japan between April 2001 and July 2014, using publicly available information. We also examined changes in the status of drug lag between Japan and the United States, as well as factors influencing drug lag. Results: This study included 120 applications for approval of oncology drugs in Japan. The median difference over a 13-year period in the approval date between the United States and Japan was 875days (29.2months). This figure peaked in 2002, and showed a tendency to decline gradually each year thereafter. In 2014, the median approval lag was 281days (9.4months). Multiple regression analysis identified the following potential factors that reduce drug lag: "Japan's participation in global clinical trials”; "bridging strategies”; "designation of priority review in Japan”; and "molecularly targeted drugs”. Conclusions: From 2001 to 2014, molecularly targeted drugs emerged as the predominant oncology drug, and the method of development has changed from full development in Japan or bridging strategy to global simultaneous development by Japan's taking part in global clinical trials. In line with these changes, the drug lag between the United States and Japan has significantly reduced to less than 1year. 
540 |a Japan Society of Clinical Oncology, 2015 
690 7 |a Anticancer drug  |2 nationallicence 
690 7 |a Clinical development  |2 nationallicence 
690 7 |a Drug lag  |2 nationallicence 
690 7 |a Japan  |2 nationallicence 
690 7 |a Oncology  |2 nationallicence 
690 7 |a PMDA  |2 nationallicence 
700 1 |a Maeda  |D Hideki  |u Division of Drug Development and Regulatory Science, Graduate School of Pharmaceutical Sciences, Keio University, 1-5-30, Shibakoen, Minato-ku, 105-8512, Tokyo, Japan  |4 aut 
700 1 |a Kurokawa  |D Tatsuo  |u Division of Drug Development and Regulatory Science, Graduate School of Pharmaceutical Sciences, Keio University, 1-5-30, Shibakoen, Minato-ku, 105-8512, Tokyo, Japan  |4 aut 
773 0 |t International Journal of Clinical Oncology  |d Springer Japan  |g 20/6(2015-12-01), 1072-1080  |x 1341-9625  |q 20:6<1072  |1 2015  |2 20  |o 10147 
856 4 0 |u https://doi.org/10.1007/s10147-015-0825-4  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
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950 |B NATIONALLICENCE  |P 700  |E 1-  |a Maeda  |D Hideki  |u Division of Drug Development and Regulatory Science, Graduate School of Pharmaceutical Sciences, Keio University, 1-5-30, Shibakoen, Minato-ku, 105-8512, Tokyo, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Kurokawa  |D Tatsuo  |u Division of Drug Development and Regulatory Science, Graduate School of Pharmaceutical Sciences, Keio University, 1-5-30, Shibakoen, Minato-ku, 105-8512, Tokyo, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t International Journal of Clinical Oncology  |d Springer Japan  |g 20/6(2015-12-01), 1072-1080  |x 1341-9625  |q 20:6<1072  |1 2015  |2 20  |o 10147