Literature DB >> 20737442

Practical issues and lessons learned from multi-regional clinical trials via case examples: a Japanese perspective.

Yuki Ando1, Toshimitsu Hamasaki.   

Abstract

The multi-regional clinical trials (MRCTs) being administered in different regions of the world now play a major role in providing evidence for the efficacy and safety of new drugs amidst the simultaneous global development and worldwide registration of such drugs, in support of the expeditious availability of medical products to patients. However, such trials present considerable challenges as far as quality, design, implementation, analysis, and interpretation are concerned. In this article, we share our observations and lessons learned from the design, implementation, analysis, and interpretation of some MRCTs with case examples. Current Japanese regulatory guidance on MRCTs is introduced along with some suggestions for design, implementation, and interpretation.
Copyright © 2010 John Wiley & Sons, Ltd.

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Year:  2010        PMID: 20737442     DOI: 10.1002/pst.448

Source DB:  PubMed          Journal:  Pharm Stat        ISSN: 1539-1604            Impact factor:   1.894


  2 in total

Review 1.  Design, data monitoring, and analysis of clinical trials with co-primary endpoints: A review.

Authors:  Toshimitsu Hamasaki; Scott R Evans; Koko Asakura
Journal:  J Biopharm Stat       Date:  2017-10-30       Impact factor: 1.051

2.  International models of investigator-initiated trials: implications for Japan.

Authors:  E L Trimble; J Ledermann; K Law; T Miyata; C K Imamura; B-H Nam; Y H Kim; Y-J Bang; M Michaels; D Ardron; S Amano; Y Ando; T Tominaga; K Kurokawa; N Takebe
Journal:  Ann Oncol       Date:  2012-07-25       Impact factor: 32.976

  2 in total

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