难治性癌症ORR达71%！再生元制药(REGN.US)双特异性抗体获FDA优先审评资格

智通财经02-22

智通财经APP获悉，2月22日，再生元制药(REGN.US)宣布，美国FDA已接受其靶向B细胞成熟抗原(BCMA)与CD3的双特异性抗体疗法linvoseltamab的生物制品许可申请(BLA)并授予优先审评资格，用以治疗患有复发/难治性(R/R)多发性骨髓瘤(MM)的成年患者，患者在接受至少三种既往疗法后发生疾病进展。该申请的PDUFA日期为2024年8月22日。据了解，...

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