中生制药(01177.HK) 公布，集团自主研发的1类创新药贝莫苏拜单抗注射液联合盐酸安罗替尼胶囊已获得中国国家药品监督管理局批准用于既往系统性抗肿瘤失败且不适合进行根治性手术治疗或根治性放疗的非微卫星高度不稳定(非MSI-H)或非错配修复基因缺陷(非dMMR)的复发性或转移性子宫内膜癌的治疗。这是贝莫苏拜单抗注射液在中国获批的第二个适应症，是盐酸安罗替尼胶囊在中国获批的第七个适应症。
除获批适应症外，贝莫苏拜单抗注射液与盐酸安罗替尼胶囊的联合疗法正在开展多项III期临床试验，涵盖一线非小细胞肺癌、非小细胞肺癌放化疗后维持、一线肾癌等多个重要领域。(sl/da)(港股报价延迟最少十五分钟。沽空资料截至 2024-11-27 12:25。)
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