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乌布雷昔替尼:首次获批。

Umbralisib: First Approval.

机构信息

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

出版信息

Drugs. 2021 May;81(7):857-866. doi: 10.1007/s40265-021-01504-2.

Abstract

Umbralisib (UKONIQ™) is an oral, first-in-class dual phosphatidylinositol 3-kinase delta (PI3Kδ) and casein kinase 1 epsilon (CK1ε) inhibitor being developed by TG Therapeutics for the treatment of various haematological malignancies. In February 2021, umbralisib received its first approval in the USA for the treatment of adults with relapsed or refractory marginal zone lymphoma (MZL) who have received ≥ 1 prior anti-CD20-based regimen, and relapsed or refractory follicular lymphoma (FL) who have received ≥ 3 prior lines of systemic therapy. Clinical studies in various haematological malignancies, including chronic lymphocytic leukaemia and non-Hodgkin's lymphoma, are underway in multiple countries. This article summarizes the milestones in the development of umbralisib leading to this first approval.

摘要

乌布雷利昔布(UKONIQ™)是一种口服、首创的双磷脂酰肌醇 3-激酶 δ(PI3Kδ)和酪蛋白激酶 1ε(CK1ε)抑制剂,由 TG Therapeutics 开发用于治疗各种血液恶性肿瘤。2021 年 2 月,乌布雷利昔布在美国首次获得批准,用于治疗接受过≥1 种基于抗 CD20 的方案治疗后复发或难治性边缘区淋巴瘤(MZL)的成年患者,以及接受过≥3 种系统性治疗方案后复发或难治性滤泡性淋巴瘤(FL)的成年患者。在多个国家,正在进行包括慢性淋巴细胞白血病和非霍奇金淋巴瘤在内的各种血液恶性肿瘤的临床研究。本文总结了乌布雷利昔布的开发里程碑,这些里程碑促成了这一首次批准。

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