Literature DB >> 20383918

International Conference on Harmonisation; Guidance on S9 Nonclincal Evaluation for Anticancer Pharmaceuticals; availability. Notice.

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Abstract

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.

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Year:  2010        PMID: 20383918

Source DB:  PubMed          Journal:  Fed Regist        ISSN: 0097-6326


  6 in total

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Review 2.  Mechanisms contributing to ado-trastuzumab emtansine-induced toxicities: a gateway to better understanding of ADC-associated toxicities.

Authors:  Yukinori Endo; Nishant Mohan; Milos Dokmanovic; Wen Jin Wu
Journal:  Antib Ther       Date:  2021-03-16

3.  Safety and activity of WX-0593 (Iruplinalkib) in patients with ALK- or ROS1-rearranged advanced non-small cell lung cancer: a phase 1 dose-escalation and dose-expansion trial.

Authors:  Yuankai Shi; Jian Fang; Xuezhi Hao; Shucai Zhang; Yunpeng Liu; Lin Wang; Jianhua Chen; Yi Hu; Xiaosheng Hang; Juan Li; Chunling Liu; Yiping Zhang; Zhehai Wang; Yanping Hu; Kangsheng Gu; Jian'an Huang; Liangming Zhang; Jinlu Shan; Weiwei Ouyang; Yanqiu Zhao; Wu Zhuang; Yan Yu; Jun Zhao; Helong Zhang; Pei Lu; Weidong Li; Meimei Si; Mingjing Ge; Huaize Geng
Journal:  Signal Transduct Target Ther       Date:  2022-01-28

4.  Exploring the Definition of "Similar Toxicities": Case Studies Illustrating Industry and Regulatory Interpretation of ICH S6(R1) for Long-Term Toxicity Studies in One or Two Species.

Authors:  Helen Prior; David O Clarke; David Jones; Eleni Salicru; Melissa M Schutten; Fiona Sewell
Journal:  Int J Toxicol       Date:  2022-04-18       Impact factor: 2.380

5.  Determination of starting dose of the T cell-redirecting bispecific antibody ERY974 targeting glypican-3 in first-in-human clinical trial.

Authors:  Shun-Ichiro Komatsu; Yoko Kayukawa; Yoko Miyazaki; Akihisa Kaneko; Hisashi Ikegami; Takahiro Ishiguro; Mikiko Nakamura; Werner Frings; Natsuki Ono; Kiyoaki Sakata; Toshihiko Fujii; Shohei Kishishita; Takehisa Kitazawa; Mika Endo; Yuji Sano
Journal:  Sci Rep       Date:  2022-07-19       Impact factor: 4.996

6.  Use of a failure probability constraint to suggest an initial dose in a phase I cancer clinical trial.

Authors:  Shu-Chen Chang; Chee-Jen Chang; Yu-Jr Lin; Ie-Bin Lian; Cathy S J Fann
Journal:  J Food Drug Anal       Date:  2014-03-12       Impact factor: 6.157

  6 in total

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