【中国生物制药(01177.HK):罗伐昔替尼临床前及临床数据在EHA 2025公布】智通财经APP讯,中国生物制药(0

智通财经
18 Jun
【中国生物制药(01177.HK):罗伐昔替尼临床前及临床数据在EHA 2025公布】智通财经APP讯,中国生物制药(01177.HK)发布公告,本集团已在2025年欧洲血液学年会(EHA)以口头报告的形式公布了罗伐昔替尼(Rovadicitinib)用于治疗急性移植物抗宿主病(aGVHD)的临床前及Ib期临床研究结果:28天总体缓解率(ORR)达84.6%,中位应答时间为4天,12个月总生存率为92.3%。

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