基石药业：CS2009II期临床试验申请获美国FDA批准

人民财讯02-16

2月16日，基石药业在港交所公告，公司核心资产CS2009（PD-1/VEGF/CTLA-4三特异性抗体）用于晚期实体瘤的II期新药临床试验（IND）申请已经获得美国食品药品监督管理局（FDA）批准。CS2009用于晚期实体瘤的II期IND申请获FDA批准，标志着这一创新免疫疗法的全球开发取得重要进展。（文章来源：人民财讯）

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