Department of Drug Metabolism & Pharmacokinetics, Genentech Inc., South San Francisco, California, USA,
AAPS J. 2013 Oct;15(4):933-40. doi: 10.1208/s12248-013-9495-1. Epub 2013 Jun 21.
The investigation of therapeutic protein drug-drug interactions has proven to be challenging. In May 2012, a roundtable was held at the American Association of Pharmaceutical Scientists National Biotechnology Conference to discuss the challenges of preclinical assessment and in vitro to in vivo extrapolation of these interactions. Several weeks later, a 2-day workshop co-sponsored by the U.S. Food and Drug Administration and the International Consortium for Innovation and Quality in Pharmaceutical Development was held to facilitate better understanding of the current science, investigative approaches and knowledge gaps in this field. Both meetings focused primarily on drug interactions involving therapeutic proteins that are pro-inflammatory cytokines or cytokine modulators. In this meeting synopsis, we provide highlights from both meetings and summarize observations and recommendations that were developed to reflect the current state of the art thinking, including a four-step risk assessment that could be used to determine the need (or not) for a dedicated clinical pharmacokinetic interaction study.
治疗性蛋白药物-药物相互作用的研究已被证明具有挑战性。2012 年 5 月,在美国药物科学家协会国家生物技术会议上举行了一次圆桌会议,讨论了这些相互作用的临床前评估和体外到体内外推的挑战。几周后,美国食品和药物管理局与国际药物创新与质量联盟共同主办了为期两天的研讨会,以促进更好地了解这一领域的当前科学、研究方法和知识空白。两次会议都主要集中在涉及治疗性蛋白的药物相互作用上,这些蛋白是促炎细胞因子或细胞因子调节剂。在本次会议摘要中,我们提供了两次会议的要点,并总结了观察结果和建议,以反映当前的最新思维,包括可用于确定是否需要(或不需要)专门的临床药代动力学相互作用研究的四步风险评估。