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Assessing the consistency of the treatment effect under the discrete random effects model in multiregional clinical trials.
Liu, Jung-Tzu; Tsou, Hsiao-Hui; Gordon Lan, K K; Chen, Chi-Tian; Lai, Yi-Hsuan; Chang, Wan-Jung; Tzeng, Chyng-Shyan; Hsiao, Chin-Fu.
Affiliation
  • Liu JT; Institute of Population Health Sciences, National Health Research Institutes, Zhunan, Taiwan.
  • Tsou HH; Institute of Bioinformatics and Structural Biology, National Tsing Hua University, Hsinchu, Taiwan.
  • Gordon Lan KK; Institute of Population Health Sciences, National Health Research Institutes, Zhunan, Taiwan.
  • Chen CT; Graduate Institute of Biostatistics, College of Public Health, China Medical University, Taichung, Taiwan.
  • Lai YH; Janssen R & D, Pharmaceutical Companies of Johnson & Johnson, Raritan, NJ, U.S.A.
  • Chang WJ; Institute of Population Health Sciences, National Health Research Institutes, Zhunan, Taiwan.
  • Tzeng CS; Software Design Center, Cloud Systems Dept. FIH Mobile Limited, New Taipei City, Taiwan.
  • Hsiao CF; Institute of Population Health Sciences, National Health Research Institutes, Zhunan, Taiwan.
Stat Med ; 35(14): 2301-14, 2016 06 30.
Article in En | MEDLINE | ID: mdl-26833851
ABSTRACT
In recent years, developing pharmaceutical products via multiregional clinical trials (MRCTs) has become standard. Traditionally, an MRCT would assume that a treatment effect is uniform across regions. However, heterogeneity among regions may have impact upon the evaluation of a medicine's effect. In this study, we consider a random effects model using discrete distribution (DREM) to account for heterogeneous treatment effects across regions for the design and evaluation of MRCTs. We derive an power function for a treatment that is beneficial under DREM and illustrate determination of the overall sample size in an MRCT. We use the concept of consistency based on Method 2 of the Japanese Ministry of Health, Labour, and Welfare's guidance to evaluate the probability for treatment benefit and consistency under DREM. We further derive an optimal sample size allocation over regions to maximize the power for consistency. Moreover, we provide three algorithms for deriving sample size at the desired level of power for benefit and consistency. In practice, regional treatment effects are unknown. Thus, we provide some guidelines on the design of MRCTs with consistency when the regional treatment effect are assumed to fall into a specified interval. Numerical examples are given to illustrate applications of the proposed approach. Copyright © 2016 John Wiley & Sons, Ltd.
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Full text: 1 Database: MEDLINE Main subject: Clinical Trials as Topic / Models, Statistical Type of study: Clinical_trials / Guideline / Risk_factors_studies Limits: Humans Language: En Journal: Stat Med Year: 2016 Type: Article Affiliation country: Taiwan

Full text: 1 Database: MEDLINE Main subject: Clinical Trials as Topic / Models, Statistical Type of study: Clinical_trials / Guideline / Risk_factors_studies Limits: Humans Language: En Journal: Stat Med Year: 2016 Type: Article Affiliation country: Taiwan