arXiv subjects

Xinru Ren

Publications and source records attributed to Xinru Ren.

3 recordsLinked to original sources

arXiv2026

Consistency Assessment of Regional Treatment Effect for Multi-Regional Clinical Trials in the Presence of Covariate Shift

Multi-Regional Clinical Trials (MRCTs) play a central role in the development of new therapies by enabling the simultaneous evaluation of drug efficacy and safety across diverse global populations. Assessing the consistency of treatment effects across regions is a fundamental aspect of MRCTs. Existing methods typically focus on region-specific marginal treatment effects. However, when treatment effect heterogeneity arises due to effect-modifying baseline covariates, distributional differences in these covariates can lead to erroneous conclusions. In this paper, we explicitly account for this phenomenon in the consistency assessment by considering the conditional average treatment effect. We propose a two-step assessment strategy that complements existing methods and mitigates the impact of treatment effect heterogeneity. Results from numerical studies demonstrate the effectiveness of the proposed approach.

stat.AP↗

arXiv2025

Consistency assessment and regional sample size calculation for MRCTs under random effects model

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.

stat.ME↗

arXiv2025

Regional consistency evaluation and sample size calculation under two MRCTs

Multi-regional clinical trial (MRCT) has been common practice for drug development and global registration. The FDA guidance `Demonstrating Substantial Evidence of Effectiveness for Human Drug and Biological Products Guidance for Industry' (FDA, 2019) requires that substantial evidence of effectiveness of a drug/biologic product to be demonstrated for market approval. In the situations where two pivotal MRCTs are needed to establish effectiveness of a specific indication for a drug or biological product, a systematic approach of consistency evaluation for regional effect is crucial. In this paper, we first present some existing regional consistency evaluations in a unified way that facilitates regional sample size calculation under the simple fixed effects model. Second, we extend the two commonly used consistency assessment criteria of MHLW (2007) in the context of two MRCTs and provide their evaluation and regional sample size calculation. Numerical studies demonstrate the proposed regional sample size attains the desired probability of showing regional consistency. A hypothetical example is presented to illustrate the application. We provide an R package for implementation.

stat.AP↗