首页> 外文会议>Conference on vaccine technology VI >VERO SF TECHNOLOGY PLATFORM: STRATEGY FOR RAPID AND EFFECTIVE VACCINE DEVELOPMENT ; FLAVIVIRUS VACCINES CASE STUDY
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VERO SF TECHNOLOGY PLATFORM: STRATEGY FOR RAPID AND EFFECTIVE VACCINE DEVELOPMENT ; FLAVIVIRUS VACCINES CASE STUDY

机译:VERO SF技术平台:快速有效的疫苗开发策略;黄病毒疫苗案例研究

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As a world leader in vaccine development, Sanofi Pasteur has acquired a strong expertise in the development and manufacturing of Vero SF-based vaccines, including against diseases of the Flavivirus family. To develop this innovative platform and provide a fast response to new viral epidemics, the vaccine manufacturing process development strategies have considerably evolved over the past decade. Toolboxes dedicated to high-throughput development have been designed and optimized to provide rapid response and effective vaccine availability. For the sake of speed and efficiency, development strategies have been reorganized by platforms. Theses platforms, such as screening, modelling, process monitoring, bioreactor, have themselves been completely redesigned to allow fast implementation of all development phases up to industrial scale. Major investments have been made in automated bioreactors and on-line analytics that enable high-throughput studies to support process definition, product characterization, ultimately moving to scale up and clinical manufacturing. Additional focus has been placed on chemically defined media definition, suitable for both cell culture and viral amplification, thus allowing higher generic development and simpler process optimization. Part of the platform considers automated bioreactors Ambr15 and 250 implemented and combined to scale up models up to 200 Liters. These models have been characterized to reduce time dedicated to scale-up studies and validation. Overall development timelines have been greatly reduced and the optimization phases reduced by a few months.
机译:作为疫苗发展的世界领导者,Sanofi Pasteur在VERO SF的疫苗的开发和制造中获得了强大的专业知识,包括针对黄病毒家族的疾病。为了开发这种创新平台并对新病毒流行病提供快速反应,疫苗制造过程开发策略在过去十年中大大进化。专用于高吞吐量开发的工具箱已经设计和优化,以提供快速响应和有效的疫苗可用性。为了速度和效率,平台重新组织了发展策略。这些平台,如筛选,建模,过程监控,生物反应器本身已经完全重新设计,以便快速实施所有开发阶段的工业规模。在自动化生物反应器和在线分析中取得了主要投资,使高通量研究能够支持流程定义,产品特征,最终迁移到扩大和临床制造。额外的焦点已置于化学定义的介质定义上,适用于细胞培养和病毒扩增,从而允许更高的通用发育和更简单的过程优化。该平台的一部分考虑了自动化生物反应器AMBR15和250实施,并结合到缩放最多200升的型号。这些模型的特点是减少致力于扩大研究和验证的时间。整体开发时间表已经大大减少,优化阶段减少了几个月。

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