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芦曲泊帕:全球首次获批。

Lusutrombopag: First Global Approval.

机构信息

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

出版信息

Drugs. 2016 Jan;76(1):155-8. doi: 10.1007/s40265-015-0525-4.

Abstract

Lusutrombopag (Mulpleta®) is an orally bioavailable, small molecule thrombopoietin (TPO) receptor agonist being developed by Shionogi for chronic liver disease (CLD) patients with thrombocytopenia prior to elective invasive surgery. Lusutrombopag acts selectively on the human TPO receptor and activates signal transduction pathways that promote the proliferation and differentiation of bone marrow cells into megakaryocytes, thereby increasing platelet levels. In September 2015, lusutrombopag received its first global approval in Japan for the improvement of CLD-associated thrombocytopenia in patients scheduled to undergo elective invasive procedures. This article summarizes the milestones in the development of lusutrombopag leading to this first approval.

摘要

芦曲泊帕(Mulpleta®)是一种口服生物利用度高的小分子血小板生成素(TPO)受体激动剂,由 Shionogi 公司研发,用于慢性肝病(CLD)患者在择期侵入性手术前的血小板减少症。芦曲泊帕选择性作用于人类 TPO 受体,激活信号转导通路,促进骨髓细胞向巨核细胞的增殖和分化,从而增加血小板水平。2015 年 9 月,芦曲泊帕在日本获得全球首次批准,用于改善计划接受择期侵入性手术的 CLD 相关血小板减少症患者的病情。本文总结了芦曲泊帕开发过程中的重要里程碑,直至获得首次批准。

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