基石药业:CS2009II期临床试验申请获美国FDA批准

人民财讯
Feb 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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