Peter te Boekhorst, MD, PhD, Erasmus University Medical Center, Rotterdam, Netherlands, introduces a Phase Ib/II trial (NCT06327100) that will evaluate the safety and efficacy of tasquinimod in patients with myelofibrosis (MF) who are refractory or intolerant to JAK2 inhibitors. The study’s primary endpoint will be a reduction in spleen volume measured by magnetic resonance imaging (MRI) after 24 weeks. This interview took place at the 29th Congress of the European Hematology Association (EHA) in Madrid, Spain.
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