Division of Medicinal Safety Science, National Institute of Health Sciences, Tonomachi 3-25-26, Kawasaki-ku, Kawasaki, Kanagawa, 210-9501, Japan.
Division of Statistical Analysis of Research Support Center, Shizuoka General Hospital, Shizuoka, Japan.
Ther Innov Regul Sci. 2021 May;55(3):523-538. doi: 10.1007/s43441-020-00246-9. Epub 2021 Jan 3.
Multi-regional clinical trials (MRCTs) are an efficient drug development strategy for eliminating drug lag in East Asian countries. In planning MRCTs according to the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use E17 guideline, it is expected that East Asian populations with relatively similar ethnicity can be pooled as one population. However, evidence supporting this assumption is limited. This study aimed to investigate population/regional differences considering influencing factors among East Asian regions using MRCT data as a research model.
A retrospective analysis was conducted to determine the efficacy of two drugs, asenapine, a schizophrenia drug, and tadalafil, a dysuria drug for benign prostatic hyperplasia, using MRCT data from Japan, Korea, and Taiwan. First, predictive factors and effect modifiers were evaluated. Then, population/regional differences were evaluated using multivariate regression models, with the interaction term Region-by-Treatment group and adjustment for influencing intrinsic/extrinsic factors.
Among the 4 outcomes for the two drugs, no significant population/regional differences were detected (P > 0.05) by the adjusted regression models. The effect modifiers, such as pretreatment drug status or concurrent diseases, were common among countries.
No significant population/regional efficacy differences were found for the two drugs among the three regions. This finding supported the possible applicability of the region pooling strategy for MRCTs in East Asia, emphasizing the benefits of exploring ethnic difference/influencing factors at an early stage to design further confirmatory studies. However, further evidence for various drugs should be accumulated.
多区域临床试验(MRCT)是消除东亚国家药物研发滞后的一种有效策略。根据人用药物国际协调会技术要求 E17 指导原则规划 MRCT 时,预计具有相对相似种族的东亚人群可以被归为一个群体。然而,支持这一假设的证据有限。本研究旨在使用 MRCT 数据作为研究模型,考察东亚地区考虑影响因素的人群/地区差异。
采用回顾性分析,利用来自日本、韩国和中国台湾的 MRCT 数据,评估两种药物(治疗精神分裂症的阿塞那平药物和治疗良性前列腺增生的尿失禁药物他达拉非)的疗效。首先,评估预测因素和效应修饰因素。然后,使用多变量回归模型评估人群/地区差异,使用交互项 Region-by-Treatment group 并调整影响内在/外在因素。
在这两种药物的 4 个结局中,调整后的回归模型未发现显著的人群/地区差异(P>0.05)。效应修饰因素,如预处理药物状态或合并疾病,在各国之间是常见的。
在这三个地区,这两种药物的疗效未发现显著的人群/地区差异。这一发现支持了东亚地区 MRCT 中区域归并策略的可能适用性,强调了在早期探索种族差异/影响因素以设计进一步验证性研究的重要性。然而,还需要进一步积累各种药物的证据。