| Literature DB >> 33423550 |
Srdan Verstovsek1, Chih-Cheng Chen2, Miklós Egyed3, Martin Ellis4, Laura Fox5, Yeow T Goh6, Vikas Gupta7, Claire Harrison8, Jean-Jacques Kiladjian9, Mihaela C Lazaroiu10, Adam Mead11, Donal McLornan12, Mary F McMullin13, Stephen T Oh14, Andrew Perkins15, Uwe Platzbecker16, Christof Scheid17, Alessandro Vannucchi18, Sung-Soo Yoon19, Mark M Kowalski20, Ruben A Mesa21.
Abstract
Hallmark features of myelofibrosis (MF) are cytopenias, constitutional symptoms and splenomegaly. Anemia and transfusion dependency are among the most important negative prognostic factors and are exacerbated by many JAK inhibitors (JAKi). Momelotinib (MMB) has been investigated in over 820 patients with MF and possesses a pharmacological and clinical profile differentiated from other JAKi by inhibition of JAK1, JAK2 and ACVR1. MMB is designed to address the complex drivers of iron-restricted anemia and chronic inflammation in MF and should improve constitutional symptoms and splenomegaly while maintaining or improving hemoglobin in JAKi-naive and previously JAKi-treated patients. The MOMENTUM Phase III study is designed to confirm and extend observations of safety and clinical activity of MMB.Entities:
Keywords: ACVR1; JAK inhibitor; Phase III clinical trial; anemia; danazol; hemoglobin; momelotinib; myelofibrosis; transfusion
Year: 2021 PMID: 33423550 DOI: 10.2217/fon-2020-1048
Source DB: PubMed Journal: Future Oncol ISSN: 1479-6694 Impact factor: 3.404