基石药业-B(02616)CS2009(PD-1/VEGF/CTLA-4三特异性抗体)II期临床试验申请获美国FDA批准

智通财经02-20

智通财经APP获悉，基石药业-B(02616)宣布公司核心资产CS2009用于晚期实体瘤的II期临床试验IND申请已经获得FDA批准。CS2009(PD-1/VEGF/CTLA-4三特异性抗体)用于晚期实体瘤的II期新药临床试验申请(IND)获美国食品药品监督管理局(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。该II期全球多中心临床试验正在澳大利亚和中国积极入组，共包含15个单药/...

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