实践中的药效测定变异性估算。

IF 1.3 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Hang Li, Tomasz M Witkos, Scott Umlauf, Christopher Thompson
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引用次数: 0

摘要

在药物开发过程中,药效测试在生物制剂生产和营销所需的质量评估中发挥着重要作用。由于多种操作和生物因素的影响,与理化方法相比,生物测定的变异性通常更高。在本文中,我们将讨论生物测定变异性的不同来源以及如何对这种变异性进行统计估算。此外,我们还提出了一种算法,用于估算与不同运行次数相关的可报告结果的变异性,以及在给定规范下相应的 OOS 率。我们对多种检测形式进行了数值实验,以阐明生物检测变异性的经验分布。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Potency Assay Variability Estimation in Practice.

During the drug development process, testing potency plays an important role in the quality assessment required for the manufacturing and marketing of biologics. Due to multiple operational and biological factors, higher variability is usually observed in bioassays compared with physicochemical methods. In this paper, we discuss different sources of bioassay variability and how this variability can be statistically estimated. In addition, we propose an algorithm to estimate the variability of reportable results associated with different numbers of runs and their corresponding OOS rates under a given specification. Numerical experiments are conducted on multiple assay formats to elucidate the empirical distribution of bioassay variability.

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来源期刊
Pharmaceutical Statistics
Pharmaceutical Statistics 医学-统计学与概率论
CiteScore
2.70
自引率
6.70%
发文量
90
审稿时长
6-12 weeks
期刊介绍: Pharmaceutical Statistics is an industry-led initiative, tackling real problems in statistical applications. The Journal publishes papers that share experiences in the practical application of statistics within the pharmaceutical industry. It covers all aspects of pharmaceutical statistical applications from discovery, through pre-clinical development, clinical development, post-marketing surveillance, consumer health, production, epidemiology, and health economics. The Journal is both international and multidisciplinary. It includes high quality practical papers, case studies and review papers.
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