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Drugs. 2015 Jan;75(1):129-39. doi: 10.1007/s40265-014-0335-0.
Nintedanib (Ofev(®)) is an orally available, small, multiple receptor tyrosine kinase inhibitor developed by Boehringer Ingelheim for the treatment of idiopathic pulmonary fibrosis (IPF) and cancer. Nintedanib received its first global approval in the US in October 2014 for the treatment of IPF. Nintedanib has received a positive opinion from the European Medicines Agency's Committee for Medicinal Products for Human Use for the treatment of IPF, and for the second-line treatment in combination with docetaxel of locally advanced, metastatic or locally recurrent non-small cell lung cancer of adenocarcinoma tumour histology. Phase 3 development programmes are also underway for colorectal cancer and ovarian cancer. Phase 2 investigation is being conducted for a variety of other solid tumours, including hepatocellular carcinoma, mesothelioma, prostate cancer, glioblastoma, renal cell carcinoma and endometrial cancer. This article summarizes the milestones in the development of nintedanib leading to this first approval for IPF.
尼达尼布(Ofev(®))是一种口服、小分子、多受体酪氨酸激酶抑制剂,由勃林格殷格翰公司开发,用于治疗特发性肺纤维化(IPF)和癌症。尼达尼布于 2014 年 10 月在美国首次获得全球批准,用于治疗 IPF。尼达尼布已获得欧洲药品管理局人用医药产品委员会的积极意见,用于治疗 IPF,以及联合多西他赛二线治疗局部晚期、转移性或局部复发性非小细胞肺癌,组织学为腺癌。还在开展 3 期开发计划用于结直肠癌和卵巢癌。正在对多种其他实体瘤进行 2 期研究,包括肝细胞癌、间皮瘤、前列腺癌、胶质母细胞瘤、肾细胞癌和子宫内膜癌。本文总结了尼达尼布开发过程中的重要里程碑,这些里程碑促成了该药首次获得 IPF 适应证的批准。