Application of the QbD Principles in the Development of the Casopitant Mesylate Manufacturing Process. Process Research Studies for the Definition of the Control Strategy of some Drug Substance-CQAs for Stages 2a, 2b, and 2c
作者:Zadeo Cimarosti、Fernando Bravo、Damiano Castoldi、Francesco Tinazzi、Stefano Provera、Alcide Perboni、Damiano Papini、Pieter Westerduin
DOI:10.1021/op1000622
日期:2010.7.16
casopitant mesylate was developed and optimised by following a Quality by Design approach, whereby a control strategy was developed, underpinned by process understanding and risk analysis, for an enhanced level of quality assurance. Quality process parameters and specifications levels for the Stages 2a, 2b, and 2c are the elements of the control strategy of the manufacturing process discussed in detail in
Casopitant被鉴定为强效NK 1葛兰素史克(GSK)的抗性药物。它被选为GSK广泛药物发现计划的一部分,因为它在许多治疗靶标上具有潜在的活性,例如炎症性肠病,膀胱过度活动症,中枢神经系统疾病等。选择casopitant的甲磺酸盐以使其充分发育。甲磺酸甲磺酸盐的生产工艺是通过遵循“按质量设计”方法开发和优化的,从而开发了以过程理解和风险分析为基础的控制策略,以提高质量保证水平。阶段2a,2b和2c的质量过程参数和规范级别是本文详细讨论的制造过程控制策略的要素。实验设计方法已被广泛用于支持该过程的公认可接受范围的定义。目的是显示为确保最终原料药的质量控制而进行的过程开发研究。