基石药业2025年中期业绩公告:创新管线加速推进,价值潜力凸显

基石药业官微
Aug 14

CS2009(PD-1/VEGF/CTLA-4三特异性抗体)的全球多中心I期研究进展顺利,截至目前在所有已评估的剂量水平中耐受性和安全性良好,并且在低剂量组的“冷肿瘤”及PD-(L)1经治患者中已观察到抗肿瘤活性,临床潜力显著。公司将在2025年欧洲内科肿瘤学会(ESMO)年会上首次揭晓CS2009的临床研究数据。CS5001(ROR1 ADC)目前临床开发进度位居全球前二,正在推进联合标准治疗...

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