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Olmutinib: First Global Approval

机译:Olmutinib:首次全球批准

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摘要

Olmutinib (Olita (TM)) is an oral, third-generation epidermal growth factor receptor tyrosine kinase inhibitor (EGFR TKI) that is being developed by Boehringer Ingelheim and Hanmi Pharmaceutical Co. Ltd for the treatment of non-small cell lung cancer (NSCLC). Third-generation EGFR TKIs with covalent binding to the receptors demonstrate irreversible enzymatic inhibition of activating EGFR mutations and T790M mutation (a common reason for acquired EGFR TKI resistance), while sparing wild-type EGFR. In December 2015, olmutinib was granted breakthrough therapy designation in NSCLC by the US FDA. In May 2016, olmutinib received its first global approval in South Korea for the treatment of patients with locally advanced or metastatic EGFR T790M mutation-positive NSCLC. This article summarizes the milestones in the development of olmutinib leading to this first approval.
机译:Olmutinib(Olita(TM))是口服的第三代表皮生长因子受体酪氨酸激酶抑制剂(EGFR TKI),由勃林格殷格翰公司和Hanmi Pharmaceutical Co. Ltd开发,用于治疗非小细胞肺癌(NSCLC) )。与受体共价结合的第三代EGFR TKI表现出不可逆的酶抑制作用,可抑制激活的EGFR突变和T790M突变(获得性EGFR TKI耐药的常见原因),同时保留野生型EGFR。 2015年12月,奥美替尼被美国FDA授予NSCLC突破性治疗称号。 2016年5月,奥尔穆替尼在韩国获得了全球首个批准,用于治疗局部晚期或转移性EGFR T790M突变阳性NSCLC患者。本文总结了导致该首次批准的olmutinib开发中的里程碑。

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