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2012 AAPS National Biotech Conference Open Forum: A Perspective on the Current State of Immunogenicity Prediction and Risk Management

机译:2012 AAPS全国生物技术会议公开论坛:免疫原性预测和风险管理的现状透视

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摘要

The immunogenicity profile of a biotherapeutic is determined by multiple product-, process- or manufacturing-, patient- and treatment-related factors and the bioanalytical methodology used to monitor for immunogenicity. This creates a complex situation that limits direct correlation of individual factors to observed immunogenicity rates. Therefore, mechanistic understanding of how these factors individually or in concert could influence the overall incidence and clinical risk of immunogenicity is crucial to provide the best benefit/risk profile for a given biotherapeutic in a given indication and to inform risk mitigation strategies. Advances in the field of immunogenicity have included development of best practices for monitoring anti-drug antibody development, categorization of risk factors contributing to immunogenicity, development of predictive tools, and development of effective strategies for risk management and mitigation. Thus, the opportunity to ask "where we are now and where we would like to go from here?" was the main driver for organizing an Open Forum on Improving Immunogenicity Risk Prediction and Management, conducted at the 2012 American Association of Pharmaceutical Scientists' (AAPS) National Biotechnology Conference in San Diego. The main objectives of the Forum include the following: to understand the nature of immunogenicity risk factors, to identify analytical tools used and animal models and management strategies needed to improve their predictive value, and finally to identify collaboration opportunities to improve the reliability of risk prediction, mitigation, and management. This meeting report provides the Forum participant's and author's perspectives on the barriers to advancing this field and recommendations for overcoming these barriers through collaborative efforts.
机译:生物治疗药物的免疫原性概况由多种产品,过程或制造,患者和治疗相关因素以及用于监测免疫原性的生物分析方法确定。这产生了复杂的情况,其限制了各个因素与观察到的免疫原性率的直接相关性。因此,对这些因素如何单独或共同影响如何影响免疫原性的总体发生率和临床风险的机械理解,对于在给定的适应症中为给定的生物治疗药物提供最佳的获益/风险概况并为降低风险的策略提供指导至关重要。免疫原性领域的进展包括开发了监测抗药物抗体发展的最佳方法,对免疫原性做出贡献的风险因素的分类,预测工具的开发以及风险管理和缓解的有效策略的发展。因此,有机会问“我们现在在哪里,我们想从这里去哪里?”是组织在2012年圣地亚哥举行的美国药物科学家协会(AAPS)全国生物技术会议上举办的“改善免疫原性风险预测和管理开放论坛”的主要推动力。论坛的主要目标包括:了解免疫原性风险因素的性质,确定使用的分析工具以及动物模型和管理策略以提高其预测价值,最后确定合作机会以提高风险预测的可靠性,缓解和管理。本次会议报告提供了论坛参与者和作者对推进该领域的障碍的观点,并提出了通过合作努力克服这些障碍的建议。

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