[创新药物对病毒和传染原的安全性评价]。

Q4 Medicine
Tetsu Kobayashi, Keisuke Yusa, Nana Kawasaki
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引用次数: 0

摘要

近年来,一些新的细胞治疗产品和生物药物正在开发中,以治疗各种以前无法治愈的疾病。关于这些创新的最重要的问题之一是如何确保在使用这些产品进行早期治疗时对包括病毒和朊病毒在内的传染性病原体的安全性。本研究的目的是对人类感染病原体的病例进行风险评估,并在国家卫生科学研究所、大学、销售许可持有人和科学学会合作的基础上提出一份风险管理计划样本。目前有三个研究课题:(1)细胞治疗产品的病毒安全性;(2)生物药物的病毒安全性;(3)朊病毒的安全性。在这份报告中,我们描述了研究对象、项目成员、研究计划大纲和正在进行的计划。基于对该项目第一年获得的文献和病例报告的回顾,还将描述病毒风险识别和细胞治疗产品风险分析的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Evaluation of the safety of innovative drugs against viruses and infectious agents].

Recently, several novel cellular therapy products and biological drugs are being developed to treat various previously untreatable diseases. One of the most important issues regarding these innovations is how to ensure safety over infectious agents, including viruses and prions, in the earliest treatments with these products. The object of this study is a risk assessment of cases of human infectious with the agents and to present a sample risk management plan based on a collaboration among the National Institute of Health Sciences, universities, marketing authorization holders, and scientific societies. There are three subjects of study: (1) the viral safety of cellular therapy products, (2) the viral safety of biological drugs, and (3) the safety of prions. In this report, we describe the objects of the study, the project members, the study plan outline, and the ongoing plans. The results of the viral risk identification and the risk analysis of cellular therapy products will also be described, based on a review of the literature and case reports obtained during the first year of this project.

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