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Myelofibrosis (MF) is a clonal myeloproliferative neoplasm, typically associated with disease-related symptoms, splenomegaly, cytopenias and bone marrow fibrosis. Patients experience a significant symptom burden and a reduced life expectancy. Patients with MF receive ruxolitinib as the current standard of care, but the depth and durability of responses and the percentage of patients achieving clinical outcome measures are limited; thus, a significant unmet medical need exists. Pelabresib is an investigational small-molecule bromodomain and extraterminal domain inhibitor currently in clinical development for MF. The aim of this article is to describe the design of the ongoing, global, phase III, double-blind, placebo-controlled MANIFEST-2 study evaluating the efficacy and safety of pelabresib and ruxolitinib versus placebo and ruxolitinib in patients with JAKi treatment-naive MF. Clinical Trial Registration: NCT04603495 (ClinicalTrials.gov)
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Harrison et al. (Thu,) studied this question.
synapsesocial.com/papers/6a1027ea5725bbd5cc609648 — DOI: https://doi.org/10.2217/fon-2022-0484
Claire Harrison
National Health Service
Vikas Gupta
Sher-e-Kashmir University of Agricultural Sciences and Technology of Jammu
Aaron T. Gerds
Cleveland Clinic
Future Oncology
University of Michigan
University of Oxford
University of Toronto
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