Fed Regist. 2010 Mar 8;75(44):10487-8.
The Food and Drug Administration (FDA) is announcing the availability of a guidance entitled "S9 Nonclinical Evaluation for Anticancer Pharmaceuticals." The guidance was prepared under the auspices of the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH). The guidance provides recommendations for nonclinical studies for the development of pharmaceuticals, including both drugs and biotechnology derived products, intended to treat patients with advanced cancer. The recommendations describe the type and timing of nonclinical studies to support an investigational new drug application (IND) and the submission of a new drug application (NDA) or biologics license application (BLA). The guidance is intended to provide information on internationally accepted recommendations for nonclinical studies to facilitate the development of anticancer pharmaceuticals.
美国食品药品监督管理局(FDA)宣布发布一份题为《S9 抗癌药物的非临床评价》的指南。该指南是在人用药品注册技术要求国际协调会议(ICH)的主持下制定的。该指南为用于治疗晚期癌症患者的药品(包括药物和生物技术衍生产品)的研发提供非临床研究建议。这些建议描述了支持研究性新药申请(IND)以及新药申请(NDA)或生物制品许可申请(BLA)提交的非临床研究的类型和时间安排。该指南旨在提供关于非临床研究国际公认建议的信息,以促进抗癌药物的研发。