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奥多柔单抗:首次获批。

Odronextamab: First Approval.

作者信息

Blair Hannah A

机构信息

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

出版信息

Drugs. 2024 Dec;84(12):1651-1658. doi: 10.1007/s40265-024-02112-6. Epub 2024 Nov 19.

Abstract

Odronextamab (Ordspono), a CD20xCD3 bispecific antibody, is being developed by Regeneron Pharmaceuticals for the treatment of B-cell non-Hodgkin's lymphoma. On 26 August 2024, odronextamab received its first approval in the EU as monotherapy for the treatment of adult patients with relapsed/refractory follicular lymphoma (FL) or relapsed/refractory diffuse large B-cell lymphoma (DLBCL) after ≥ 2 lines of systemic therapy. Clinical trials in various other B-cell non-Hodgkin's lymphoma, including mantle cell lymphoma, marginal zone lymphoma and chronic lymphocytic leukaemia, are underway in multiple countries. This article summarizes the milestones in the development of odronextamab leading to this first approval for the treatment of adult patients with relapsed/refractory FL or relapsed/refractory DLBCL.

摘要

奥多雷西单抗(Ordspono)是一种CD20×CD3双特异性抗体,由再生元制药公司研发,用于治疗B细胞非霍奇金淋巴瘤。2024年8月26日,奥多雷西单抗在欧盟首次获批,作为单药疗法用于治疗接受过≥2线全身治疗后的复发/难治性滤泡性淋巴瘤(FL)或复发/难治性弥漫性大B细胞淋巴瘤(DLBCL)的成年患者。多个国家正在进行针对其他多种B细胞非霍奇金淋巴瘤的临床试验,包括套细胞淋巴瘤、边缘区淋巴瘤和慢性淋巴细胞白血病。本文总结了奥多雷西单抗研发过程中的里程碑事件,这些事件促成了其首次获批用于治疗复发/难治性FL或复发/难治性DLBCL的成年患者。

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