Lorlatinib: First Global Approval

Lorlatinib: First Global Approval
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DOI:
10.1007/s40265-018-1041-0
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发表时间:
2019-01-01
期刊:
影响因子:
11.5
通讯作者:
Syed, Yahiya Y.
Syed, Yahiya Y.
中科院分区:
医学1区
文献类型:
--
作者:
Syed, Yahiya Y.

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Lorlatinib是辉瑞公司开发的间变性淋巴瘤激酶(ALK)和C-ros癌基因1(ROS1)激酶的口服小分子抑制剂,用于治疗ALK阳性非小细胞肺癌(NSCLC)。根据 I/II 期试验的结果,lorlatinib 于 2018 年 9 月在日本获得批准,并于 2018 年 11 月在美国获得批准用于治疗 ALK 阳性 NSCLC。本文总结了 lorlatinib 开发过程中的里程碑,导致该适应症首次获得全球批准。
Lorlatinib is an oral small molecule inhibitor of anaplastic lymphoma kinase (ALK) and C-ros oncogene 1 (ROS1) kinase developed by Pfizer for the treatment of ALK-positive non-small cell lung cancer (NSCLC). Based on results from a phase I/II trial, lorlatinib received approval in Japan in September 2018 and in the USA in November 2018 for the treatment of ALK-positive NSCLC. This article summarizes the milestones in the development of lorlatinib leading to the first global approval for this indication.