第六章-临床试验和超说明书用药

Giovanni Maria Cavo
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引用次数: 0

摘要

该贡献旨在分析一个与实验主题密切相关的主题,即在接受药物治疗的患者的保护方面:标签外药物的使用,即总结而言,将药物用于未包括在药物上市许可(ma)范围内的治疗适应症的可能性。从欧洲人用药物的纪律出发,分析重点放在意大利立法的特殊性上,意大利立法代表了欧洲标签外规则的一个标志性案例。特别关注的是药物Avastin R©和Lucentis R©,近年来突出了国家立法的局限性,包括可能与欧洲法规形成对比。特别是,立法者的选择,最近由意大利宪法法院支持,提交的可能性,以及什么是“标签外”药物的安全性和有效性的最低要求的定义,可以开给病人,是我们打算激发读者反思的主要问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chapter 6 - Clinical trials and off-label use of drugs
The contribution aims to analyze a topic closely related to the subject of experimentation, in terms of protection of patients undergoing drug therapy: the use of off-label drugs, that is, in summary, the possibility to use a medicine for therapeutic indications not covered within the marketing authorisation (M.A.) of the drug. Moving from European discipline on medicines for human use, the analysis focuses on the peculiarities of the Italian legislation, representing in Europe an emblematic case of off-label rules. A particular focus is dedicated to the case of drugs Avastin R © and Lucentis R © , which in recent years has highlighted the limits of that national legislation, including the possible contrast with European regulations. In particular, the choice of legislator, recently upheld by the Italian Constitutional Court, to submit the possibility, as well as the definition of what are the minimum requirements of safety and efficacy for a drug “off-label” may be prescribed to patients, are the main issues on which we intend to stimulate reflection on the reader.
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