Core Viewpoint - The approval of a new indication for Sugli monoclonal antibody by the European Commission marks a significant advancement for the company, providing new treatment options for a broader patient population with advanced non-small cell lung cancer (NSCLC) [1] Company Summary - 基石药业-B (02616) experienced a stock price increase of nearly 7% during trading, closing up 5.22% at HKD 6.25, with a trading volume of HKD 39.03 million [1] - The European Commission has approved Sugli monoclonal antibody for the treatment of adult patients with unresectable stage III non-small cell lung cancer (NSCLC) who have PD-L1 expression ≥1%, no EGFR sensitive mutations or ALK, ROS1 genomic alterations, and have not shown disease progression after platinum-based chemoradiotherapy [1] - The CEO of the company, Dr. Yang Jianxin, highlighted that this new indication approval comes just one year after the initial approval for first-line treatment of metastatic squamous and non-squamous NSCLC, indicating comprehensive coverage from stage III to IV NSCLC in Europe [1] Industry Summary - The approval signifies a broader treatment landscape for NSCLC patients in Europe, enhancing the accessibility of Sugli monoclonal antibody globally [1]
港股异动 | 基石药业-B(02616)现涨超5% 欧盟委员会批准舒格利单抗用于治疗III期非小细胞肺癌