Schwenke James, Stroup Walter, Quinlan Michelle, Forenzo Patrick
Applied Research Consultants, LLC, 119 Town Farm Road, New Milford, Connecticut, 06776-3718, USA.
Statistics, University of Nebraska-Lincoln, Lincoln, Nebraska, USA.
AAPS PharmSciTech. 2023 Mar 21;24(4):80. doi: 10.1208/s12249-023-02532-9.
Methods for estimating pharmaceutical shelf life based on tolerance intervals are proposed by Schwenke, et al. AAPS PharmSciTech. 2020;21:290, [1] where a critical quality attribute that follows a simple linear (straight line) response trend across storage time is presented as the traditional example. A random coefficient mixed linear regression model is used to characterize the between batch and within batch variation. These methods are further discussed for various stability study scenarios, number of stability batches, and levels of assumed risk in Schwenke, et al. AAPS PharmSciTech. 2021;22:273, [4] through a simulation study, again based on a critical quality attribute assuming a simple linear response. However, in practice, not all stability response profiles conveniently follow straight line or linear trends. The purpose of this paper is to extend the proposed tolerance interval and random coefficient mixed regression methods for estimating pharmaceutical shelf life to critical quality attributes that follow more complex stability response profiles. As an example, a nonlinear response is typically characterized by either an increasing or decreasing response, starting from an initial concentration, trending with storage time towards some limiting response or asymptote. Nonlinear responses cannot be statistically analyzed with linear model methods. Practical information supported by simulation results based on a pharmaceutical stability study are discussed to allow for appropriate statistical analyses and shelf life estimates through random coefficient mixed nonlinear regression and tolerance interval methods.
施温克等人提出了基于容忍区间估计药品货架期的方法。《AAPS药物科学与技术》,2020年;21:290,[1] 其中给出了一个关键质量属性作为传统示例,该属性在储存时间内呈现简单线性(直线)响应趋势。使用随机系数混合线性回归模型来表征批次间和批次内的变异性。施温克等人在《AAPS药物科学与技术》,2021年;22:273,[4] 中通过模拟研究,再次基于假设简单线性响应的关键质量属性,针对各种稳定性研究场景、稳定性批次数量和假设风险水平对这些方法进行了进一步讨论。然而,在实际中,并非所有稳定性响应曲线都能方便地遵循直线或线性趋势。本文的目的是将所提出的用于估计药品货架期的容忍区间和随机系数混合回归方法扩展到具有更复杂稳定性响应曲线的关键质量属性。例如,非线性响应通常表现为从初始浓度开始,响应增加或减少,随储存时间趋向于某个极限响应或渐近线。线性模型方法无法对非线性响应进行统计分析。本文讨论了基于药物稳定性研究的模拟结果所支持的实际信息,以便通过随机系数混合非线性回归和容忍区间方法进行适当的统计分析和货架期估计。