辉瑞与礼来达成18亿美元交易降低Tanezumab风险

Heather Cartwright
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引用次数: 0

摘要

三年前,由于严重的安全问题,美国FDA暂停了所有神经生长因子(NGF)抑制剂的临床开发,辉瑞公司决定与礼来公司合作继续其抗NGF抗体tanezumab的III期开发,这是一项潜在价值高达18亿美元的交易的一部分。2012年3月,FDA咨询委员会同意NGF抑制剂可以在某些患者群体中进行研究。辉瑞希望在2014年上半年向FDA提交非临床数据后,恢复该药治疗骨关节炎、慢性腰痛和癌症疼痛的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pfizer Mitigates Tanezumab Risk with Potential US$1.8 B Deal with Eli Lilly
Three years after development of the entire class of nerve growth factor (NGF) inhibitors was put on clinical hold by the US FDA over serious safety concerns related to joint destruction, Pfizer has decided to continue Phase III development of its anti-NGF antibody tanezumab in collaboration with Eli Lilly as part of a deal potentially worth up to US$1.8 B. In March 2012, an FDA advisory committee agreed that NGF inhibitors could be studied in certain patient populations. Pfizer hopes to resume studies of the drug in osteoarthritis, chronic low back pain and cancer pain after submitting nonclinical data to the FDA in the first half of 2014.
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