百时美施贵宝（Bristol Myers Squibb）公司周一宣布，评估Breyanzi药物用于治疗复发难治性惰性B细胞非霍奇金淋巴瘤成人患者的 TRANSCEND FL二期试验在边缘区淋巴瘤队列研究中达到了主要终点。

　　该2期试验显示了具有统计学和临床意义的总体缓解率（ORR）。它还达到了完全缓解率（CRR）的关键次要终点，未观察到新的安全性信号。

　　百时美施贵宝公司指出：“凭借这些数据，Breyanzi证明了其针对第五种癌症类型的疗效和可控的安全性，这是所有针对CD19的CAR-T细胞疗法中数据最高的。”

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