治疗非小细胞肺癌,武田“first-in-class”精准疗法获FDA加速批准
参考资料:
[1] Takeda’s EXKIVITY™ (mobocertinib) Approved by U.S. FDA as the First Oral Therapy Specifically Designed for Patients with EGFR Exon20 Insertion+ NSCLC. Retrieved September 15, 2021, from https://www.businesswire.com/news/home/20210915006101/en
[2] Takeda Presents Positive Results For Mobocertinib in Patients with EGFR Exon20 insertion+ mNSCLC Who Received Prior Platinum-based Chemotherapy. Retrieved January 28, 2021, from https://www.businesswire.com/news/home/20210128005072/en
来源:药明康德
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