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Main Authors: Ren, Xinru, Xu, Jin
Format: Preprint
Published: 2025
Subjects:
Online Access:https://arxiv.org/abs/2508.09443
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author Ren, Xinru
Xu, Jin
author_facet Ren, Xinru
Xu, Jin
contents Multi-regional clinical trials (MRCTs) have become common practice for drug development and global registration. Once overall significance is established, demonstrating regional consistency is critical for local health authorities. Methods for evaluating such consistency and calculating regional sample sizes have been proposed based on the fixed effects model using various criteria. To better account for the heterogeneity of treatment effects across regions, the random effects model naturally arises as a more effective alternative for both design and inference. In this paper, we present the design of the overall sample size along with regional sample fractions. We also provide the theoretical footage for assessing consistency probability using Method 1 of MHLW (2007), based on the empirical shrinkage estimator. The latter is then used to determine the regional sample size of interest. We elaborate on the applications to common continuous, binary, and survival endpoints in detail. Simulation studies show that the proposed method retains the consistency probability at the desired level. We illustrate the application using a real cardiovascular outcome trial in diabetes. An R package is provided for implementation.
format Preprint
id arxiv_https___arxiv_org_abs_2508_09443
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Consistency assessment and regional sample size calculation for MRCTs under random effects model
Ren, Xinru
Xu, Jin
Methodology
Applications
Multi-regional clinical trials (MRCTs) have become common practice for drug development and global registration. Once overall significance is established, demonstrating regional consistency is critical for local health authorities. Methods for evaluating such consistency and calculating regional sample sizes have been proposed based on the fixed effects model using various criteria. To better account for the heterogeneity of treatment effects across regions, the random effects model naturally arises as a more effective alternative for both design and inference. In this paper, we present the design of the overall sample size along with regional sample fractions. We also provide the theoretical footage for assessing consistency probability using Method 1 of MHLW (2007), based on the empirical shrinkage estimator. The latter is then used to determine the regional sample size of interest. We elaborate on the applications to common continuous, binary, and survival endpoints in detail. Simulation studies show that the proposed method retains the consistency probability at the desired level. We illustrate the application using a real cardiovascular outcome trial in diabetes. An R package is provided for implementation.
title Consistency assessment and regional sample size calculation for MRCTs under random effects model
topic Methodology
Applications
url https://arxiv.org/abs/2508.09443