Lamb Yvette N
Springer Nature, Private Bag 65901, Mairangi Bay, Auckland, 0754, New Zealand.
Drugs. 2024 Dec;84(12):1665-1671. doi: 10.1007/s40265-024-02120-6. Epub 2024 Nov 26.
Fulzerasib (Dupert; Innovent Biologics/GenFleet Therapeutics) is an orally active small molecule inhibitor of the KRAS G12C mutant protein being developed for the treatment of solid tumors harboring the KRAS G12C oncogenic driver mutation, including non-small cell lung cancer (NSCLC) and colorectal cancer. Fulzerasib received its first approval on 21 August 2024 in China, for the treatment of adults with KRAS G12C-mutated advanced NSCLC who have received at least one line of systemic therapy. This conditional approval was based on the positive results of a single-arm, phase II study. This article summarizes the milestones in the development of fulzerasib leading to this first approval for KRAS G12C-mutated advanced NSCLC.
伏泽拉西布(都伯特;信达生物/健飞医药)是一种口服活性小分子抑制剂,可抑制KRAS G12C突变蛋白,正被开发用于治疗携带KRAS G12C致癌驱动突变的实体瘤,包括非小细胞肺癌(NSCLC)和结直肠癌。伏泽拉西布于2024年8月21日在中国首次获批,用于治疗接受过至少一线全身治疗的KRAS G12C突变的晚期NSCLC成人患者。该附条件批准基于一项单臂II期研究的阳性结果。本文总结了伏泽拉西布在开发过程中取得的里程碑式进展,这些进展促成了其首次获批用于KRAS G12C突变的晚期NSCLC。