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基于模型的高变异性药物高效生物等效性研究设计方法

Model-Based Approach for Designing an Efficient Bioequivalence Study for Highly Variable Drugs.

作者信息

Song Eunjung, Lee Woojoo, Kim Bo-Hyung

机构信息

Department of Clinical Pharmacology and Therapeutics, Kyung Hee University Medical Center, Seoul 02447, Korea.

Department of Public Health Sciences, Graduate School of Public Health, Seoul National University, Seoul 08826, Korea.

出版信息

Pharmaceuticals (Basel). 2021 Oct 28;14(11):1101. doi: 10.3390/ph14111101.

Abstract

The statistical procedures as outlined by the European Medicines Agency (EMA) and United States Food and Drug Administration (FDA) guidelines for bioequivalence testing of highly variable drugs (HVDs) are complex. Additionally, the sample size is affected by clinical study designs or practical real-world problems, such as dropout rate or study budget. To overcome these difficulties, we propose a model-based approach for the selection of a study design with a sample size that satisfies the bioequivalence criteria using simulation studies based on a pharmacokinetic (PK) model. The designed approach was implemented using a simulation procedure considering some conventionally measured factors, such as geometric mean ratio and within-subject coefficient of variation, with various PK information important in determining bioequivalence. All simulation results were assessed according to the EMA and FDA guidelines. Furthermore, power calculations from simulation results were interpreted with regard to PK characteristics and compared among 2 × 2, 3 × 3, and 2 × 4 crossover designs to determine the efficient design considering appropriate sample size and duration of the clinical study. The proposed approach can be applied to bioequivalence studies of all drugs. However, the current study was targeted at HVDs, which are highly likely to require detailed decision making for sample size and study design.

摘要

欧洲药品管理局(EMA)和美国食品药品监督管理局(FDA)针对高变异药物(HVDs)生物等效性测试所概述的统计程序很复杂。此外,样本量会受到临床研究设计或实际现实问题的影响,如脱落率或研究预算。为克服这些困难,我们提出一种基于模型的方法,通过基于药代动力学(PK)模型的模拟研究,选择具有满足生物等效性标准样本量的研究设计。所设计的方法是通过考虑一些常规测量因素(如几何平均比值和受试者内变异系数)的模拟程序来实施的,同时还考虑了在确定生物等效性方面重要的各种PK信息。所有模拟结果均根据EMA和FDA指南进行评估。此外,根据PK特征对模拟结果进行功效计算,并在2×2、3×3和2×4交叉设计之间进行比较,以确定考虑适当样本量和临床研究持续时间的有效设计。所提出的方法可应用于所有药物的生物等效性研究。然而,当前研究针对的是高变异药物,这类药物极有可能在样本量和研究设计方面需要进行详细决策。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf39/8624447/f85b02387dca/pharmaceuticals-14-01101-g001.jpg

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