美国食品药品监督管理局（FDA）已正式受理施贵宝（Bristol-Myers Squibb）提交的新药Iberdomide上市申请，该药物旨在治疗复发或难治性多发性骨髓瘤患者。这一进展标志着施贵宝在血液肿瘤领域研发的重要里程碑，为患者提供了新的治疗希望。
多发性骨髓瘤作为一种恶性血液疾病，复发或难治性病例的治疗选择有限，临床需求迫切。Iberdomide作为一种创新疗法，其申请获受理意味着FDA将基于现有数据展开审评，未来可能加速该药物的上市进程。施贵宝持续投入研发，展现了其在肿瘤治疗领域的战略布局与执行力。
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