Literature DB >> 25560978

Regulatory review time for approval of oncology drugs in Japan between 2001 and 2014. Considerations of changes, factors that affect review time, and difference with the United States.

Hideki Maeda1, Tatsuo Kurokawa.   

Abstract

In this study, we comprehensively and historically studied the review time of oncology drugs approved by the regulatory authorities in Japan with publicly available information. A total of 120 applications of oncology drugs were approved in Japan between April 2001 and July 2014. The review time peaked with 732.0 days (24.4 months) in 2005, and showed a tendency to decline gradually each year thereafter. After 2012, a significant reduction of the review time was seen in comparison to the median of 13-year median time. In addition, we compared the review time with that in the United States. The median review time lag with the United States was significantly peaked in 2005. After 2005, the review time lag with the FDA has decreased, but lag did not significantly reduce by 2014. We also examined factors influencing the review time in Japan with multiple regression analysis. It was found that the factors related to a use of overseas data and expedited program for accelerating the reviews influenced the direction of shortening the review time. We consider that regulatory authorities in Japan need to keep making efforts to reduce the review time further and eliminate the review time lag with the United States.
© 2015, The American College of Clinical Pharmacology.

Keywords:  Japan; PMDA; drug lag; oncology; regulatory review

Mesh:

Substances:

Year:  2015        PMID: 25560978     DOI: 10.1002/jcph.458

Source DB:  PubMed          Journal:  J Clin Pharmacol        ISSN: 0091-2700            Impact factor:   3.126


  4 in total

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

Authors:  Hideki Maeda; Tatsuo Kurokawa
Journal:  Int J Clin Oncol       Date:  2015-04-03       Impact factor: 3.402

Review 2.  A perspective on the benefit-risk assessment for new and emerging pharmaceuticals in Japan.

Authors:  Tetsuya Tanimoto
Journal:  Drug Des Devel Ther       Date:  2015-03-31       Impact factor: 4.162

3.  How are new drugs disseminated in Japan? Analysis using the National Database of Health Insurance Claims of Japan.

Authors:  Tomone Watanabe; Takehiro Sugiyama; Kenjiro Imai; Takahiro Higashi
Journal:  Cancer Sci       Date:  2022-03-28       Impact factor: 6.518

Review 4.  Toward Optimum Benefit-Risk and Reduced Access Lag For Cancer Drugs in Asia: A Global Development Framework Guided by Clinical Pharmacology Principles.

Authors:  K Venkatakrishnan; C Burgess; N Gupta; A Suri; T Takubo; X Zhou; D DeMuria; M Lehnert; K Takeyama; S Singhvi; A Milton
Journal:  Clin Transl Sci       Date:  2016-02-05       Impact factor: 4.689

  4 in total

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