文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

依马芦单抗:全球首次获批。

Emapalumab: First Global Approval.

机构信息

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

出版信息

Drugs. 2019 Jan;79(1):99-103. doi: 10.1007/s40265-018-1046-8.


DOI:10.1007/s40265-018-1046-8
PMID:30623346
Abstract

Emapalumab-Izsg (hereafter referred to as emapalumab) [Gamifant] is a monoclonal antibody directed against interferon gamma that is available as an intravenous infusion. Emapalumab is being developed by Novimmune and Swedish Orphan Biovitrum for the treatment of haemophagocytic lymphohistiocytosis (HLH). In November 2018, emapalumab received its first global approval in the USA, for the treatment of paediatric (newborn and older) and adult patients with primary HLH, who have refractory, recurrent or progressive disease or intolerance to conventional HLH therapy. Emapalumab is under regulatory review in the EU for the treatment of primary HLH. This article summarizes the milestones in the development of emapalumab leading to this first global approval for HLH in the USA.

摘要

依帕珠单抗-IZSG(以下简称依帕珠单抗)[Gamifant]是一种针对干扰素 γ 的单克隆抗体,可通过静脉输注给药。依帕珠单抗由诺华免疫公司和瑞典 Orphan Biovitrum 公司开发,用于治疗噬血细胞性淋巴组织细胞增生症(HLH)。2018 年 11 月,依帕珠单抗在美国获得全球首次批准,用于治疗新生儿和年龄较大的儿童以及成人原发性 HLH 患者,这些患者患有难治性、复发性或进行性疾病,或对常规 HLH 治疗不耐受。依帕珠单抗正在欧盟接受监管审查,用于治疗原发性 HLH。本文总结了依帕珠单抗开发过程中的重要里程碑,这些进展促成了该药在美国的 HLH 全球首次批准。

相似文献

[1]
Emapalumab: First Global Approval.

Drugs. 2019-1

[2]
Emapalumab in Children with Primary Hemophagocytic Lymphohistiocytosis.

N Engl J Med. 2020-5-7

[3]
Emapalumab for the treatment of hemophagocytic lymphohistiocytosis.

Drugs Today (Barc). 2020-7

[4]
Emapalumab for adult and pediatric patients with hemophagocytic lymphohistiocytosis.

Expert Rev Clin Pharmacol. 2021-5

[5]
Novel Therapeutic Approaches to Familial HLH (Emapalumab in FHL).

Front Immunol. 2020-12-2

[6]
Emapalumab for the treatment of relapsed/refractory hemophagocytic lymphohistiocytosis.

Blood. 2019-11-21

[7]
Real-world treatment patterns and outcomes in patients with primary hemophagocytic lymphohistiocytosis treated with emapalumab.

Blood Adv. 2024-5-14

[8]
Thinking Beyond HLH: Clinical Features of Patients with Concurrent Presentation of Hemophagocytic Lymphohistiocytosis and Thrombotic Microangiopathy.

J Clin Immunol. 2020-7

[9]
Treatment of refractory hemophagocytic lymphohistiocytosis with emapalumab despite severe concurrent infections.

Blood Adv. 2019-1-8

[10]
Emapalumab as a therapeutic intervention for Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis: A case series.

Medicine (Baltimore). 2024-9-27

引用本文的文献

[1]
Neurological Complications in Inborn Errors of Immunity: A Scoping Review of Clinical Spectrum, Pathophysiological Mechanisms, and Therapeutic Strategies.

Clin Rev Allergy Immunol. 2025-7-18

[2]
Latest updates on pathogenesis mechanisms and management strategies for cytokine release syndrome, neurotoxicity, and hemophagocytic lymphohistiocytosis related to CAR-T cell therapies.

Ann Hematol. 2025-6-19

[3]
Deep insight into cytokine storm: from pathogenesis to treatment.

Signal Transduct Target Ther. 2025-4-16

[4]
CXCL9 and IL-18: potential biomarkers for efficacy evaluation in refractory hemophagocytic lymphohistiocytosis treated with RED (ruxolitinib, emapalumab and dexamethasone).

Ann Hematol. 2025-3

[5]
Efficacy of emapalumab in the management of anti‑CD19 chimeric antigen receptor T‑cell therapy‑associated cytokine release syndrome: A report of two cases.

Oncol Lett. 2024-11-22

[6]
Hemophagocytic lymphohistiocytosis: current treatment advances, emerging targeted therapy and underlying mechanisms.

J Hematol Oncol. 2024-11-7

[7]
Therapeutic antibodies in oncology: an immunopharmacological overview.

Cancer Immunol Immunother. 2024-10-3

[8]
Emapalumab as a therapeutic intervention for Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis: A case series.

Medicine (Baltimore). 2024-9-27

[9]
[Hemophagocytic syndrome secondary to invasive NK cell leukemia and T-cell lymphoma treated with the modified MINE protocol: report of three cases and literature review].

Zhonghua Xue Ye Xue Za Zhi. 2024-6-14

[10]
IL-1 Family Blockade in Cytokine Storm Syndromes.

Adv Exp Med Biol. 2024

本文引用的文献

[1]
Neutralization of IFN-γ reverts clinical and laboratory features in a mouse model of macrophage activation syndrome.

J Allergy Clin Immunol. 2017-8-12

[2]
A consensus review on malignancy-associated hemophagocytic lymphohistiocytosis in adults.

Cancer. 2017-9-1

[3]
Neutralization of IFNgamma defeats haemophagocytosis in LCMV-infected perforin- and Rab27a-deficient mice.

EMBO Mol Med. 2009-5

[4]
An animal model of hemophagocytic lymphohistiocytosis (HLH): CD8+ T cells and interferon gamma are essential for the disorder.

Blood. 2004-8-1

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索