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寡核苷酸安全工作组夸大了药理学小组委员会共识文件。

Oligo safety working group exaggerated pharmacology subcommittee consensus document.

机构信息

Preclinsight, Reno, Nevada 89502, USA.

出版信息

Nucleic Acid Ther. 2013 Feb;23(1):21-8. doi: 10.1089/nat.2012.0399. Epub 2013 Jan 4.

Abstract

This document summarizes the current consensus opinion of the Exaggerated Pharmacology (EP) Subcommittee of the Oligonucleotide Safety Working Group on the appropriate strategies to assess potential adverse effects caused by an "exaggerated" degree of the intended pharmacologic activity of an oligonucleotide (ON). The Subcommittee focused its discussions primarily on the ON subclasses that impact expression of "host" (i.e., human gene products--antisense, small interfering RNAs, and related ONs that target messenger RNA), with later and more limited discussions on aptamer, immunostimulatory, and microRNA subclasses. It is expected that many of these principles will be relevant to other subclasses but will need to be carefully considered as those development programs advance towards clinical trials. The recommendations may also serve as a frame of reference when designing Good Laboratory Practice safety studies with ONs, with regard to the study design elements that address assessment of EP. It is also hoped that these recommendations will establish a foundation for discussion with regulatory agencies on this subject.

摘要

本文档总结了寡核苷酸安全工作组夸大药理学(EP)小组委员会目前对评估“夸大”程度的寡核苷酸(ON)预期药理学活性引起的潜在不良反应的适当策略的共识意见。小组委员会的讨论主要集中在影响“宿主”(即人类基因产物-反义、小干扰 RNA 和靶向信使 RNA 的相关 ON)表达的 ON 亚类上,后来对适体、免疫刺激和 microRNA 亚类进行了更有限的讨论。预计这些原则中的许多将与其他亚类相关,但在这些开发计划推进到临床试验时,需要仔细考虑。这些建议也可以作为在设计具有 ON 的良好实验室规范安全性研究时的参考框架,考虑到解决 EP 评估的研究设计要素。我们还希望这些建议将为与监管机构就此主题进行讨论奠定基础。

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