赛诺菲(SNY.US)Sarclisa获FDA优先审查用于治疗多发性骨髓瘤

智通财经05-27

智通财经APP获悉，赛诺菲(SNY.US)宣布，其Sarclisa的补充生物制品许可申请 (sBLA)已获得美国FDA优先审查，用于联合硼替佐米、来那度胺和地塞米松治疗不适合移植的新诊断多发性骨髓瘤患者。多发性骨髓瘤是一种恶性浆细胞病。赛诺菲表示，FDA决定的目标行动日期为2024年9月27日。该公司补充说，欧盟也在审查一份监管意见书。

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赛诺菲(SNY.US)Sarclisa获FDA优先审查 用于治疗多发性骨髓瘤

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赛诺菲(SNY.US)Sarclisa获FDA优先审查用于治疗多发性骨髓瘤