Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX.
Blood. 2024 Aug 15;144(7):708-713. doi: 10.1182/blood.2023023719.
In September 2023, the US Food and Drug Administration approved momelotinib for the treatment of myelofibrosis (MF) with anemia, marking the fourth US regulatory approval of a Janus kinase inhibitor for MF. A positive opinion from the European Medicines Agency followed in November 2023. Momelotinib's ability to address splenomegaly, symptoms, and anemia, including in patients with thrombocytopenia (with platelet counts of ≥25 × 109/L), the ease of switching from ruxolitinib, and good tolerability uniquely position it to substantially impact the MF treatment landscape.
2023 年 9 月,美国食品药品监督管理局批准 momelotinib 用于治疗伴贫血的骨髓纤维化(MF),这是第四款获得美国监管机构批准用于 MF 的 JAK 抑制剂。2023 年 11 月,欧洲药品管理局也给出了积极意见。momelotinib 具有缩小脾脏、改善症状和贫血的能力,包括血小板计数≥25×109/L 的患者,与 ruxolitinib 转换方便,且具有良好的耐受性,这些独特的优势使其能够显著改变 MF 的治疗格局。