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Drugs. 2022 May;82(7):831-838. doi: 10.1007/s40265-022-01718-y.
Pacritinib (VONJO™) is an orally administered, small molecule kinase inhibitor being developed by CTI BioPharma for the treatment of myelofibrosis and graft-versus-host disease. Pacritinib received its first approval in February 2022 in the USA for the treatment of adults with intermediate- or high-risk primary or secondary (post-polycythemia vera or post-essential thrombocythemia) myelofibrosis with a platelet count below 50 × 10/L. The accelerated approval was based on results from the randomized, active-controlled, phase III PERSIST-2 trial, in which spleen volume reduction was demonstrated in pacritinib recipients. This article summarizes the milestones in the development of pacritinib leading to this first approval for myelofibrosis.
帕克里替尼(VONJO™)是一种口服小分子激酶抑制剂,由 CTI BioPharma 开发,用于治疗骨髓纤维化和移植物抗宿主病。帕克里替尼于 2022 年 2 月在美国首次获得批准,用于治疗血小板计数低于 50×10/L 的中高危原发性或继发性(真性红细胞增多症后或原发性血小板增多症后)骨髓纤维化的成年患者。加速批准基于随机、活性对照、III 期 PERSIST-2 试验的结果,该试验表明帕克里替尼治疗组的脾脏体积缩小。本文总结了帕克里替尼开发过程中的重要里程碑,最终使其在骨髓纤维化方面获得首次批准。