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奥贝卡替吉仑自体白细胞介素-2:首次获批。

Obecabtagene Autoleucel: First Approval.

作者信息

Lee Arnold

机构信息

Springer Nature, Private Bag 65901, Mairangi Bay, Auckland, 0754, New Zealand.

出版信息

Mol Diagn Ther. 2025 May;29(3):419-423. doi: 10.1007/s40291-025-00771-z. Epub 2025 Jan 31.

Abstract

Obecabtagene autoleucel (AUCATZYL) is a CD19-directed genetically modified autologous T cell immunotherapy which is being developed by Autolus for the treatment of hematological cancers and systemic lupus erythematosus. In comparison with other chimeric antigen receptor T (CAR T) therapies, obecabtagene autoleucel has a fast off-rate binder for CD19. Obecabtagene autoleucel received approval following positive results from the FELIX phase I/II trial in adults with relapsed or refractory B-cell precursor acute lymphoblastic leukemia (ALL), and it is the first CAR T therapy that does not have mandatory Risk Evaluation Mitigation Strategy monitoring requirements. This article summarizes the milestones in the development of obecabtagene autoleucel leading to this first approval for the treatment of adults with relapsed or refractory B-cell precursor ALL.

摘要

奥贝卡他基因自体白细胞介素(AUCATZYL)是一种靶向CD19的基因修饰自体T细胞免疫疗法,由Autolus公司研发,用于治疗血液系统癌症和系统性红斑狼疮。与其他嵌合抗原受体T(CAR T)疗法相比,奥贝卡他基因自体白细胞介素对CD19具有快速解离速率的结合物。在针对复发或难治性B细胞前体急性淋巴细胞白血病(ALL)成人患者的FELIX I/II期试验取得阳性结果后,奥贝卡他基因自体白细胞介素获得批准,它是首个没有强制性风险评估缓解策略监测要求的CAR T疗法。本文总结了奥贝卡他基因自体白细胞介素研发过程中的重要节点,这些节点促成了其首次获批用于治疗复发或难治性B细胞前体ALL成人患者。

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