Tasquinimod in Patients with Myelofibrosis Refractory to or Intolerant for JAK2 Inhibition

The goal of this clinical trial is to learn if therapy can be improved in patients with myelofibrosis (MF) who have primary resistance or who have progressed after treatment with a Janus kinase (JAK) inhibitor or are intolerant for this category of drugs. The main questions it aims to answer are: * To evaluate the feasibility and safety of once daily dose of tasquinimod for 24 weeks (6 cycles) * To determine the optimal dose Patients will be treated once daily with tasquinimod for a maximum period of 24 weeks (6 cycles). During the study most (diagnostic) procedures are part of the standard of care. Different from standard of care: * Participation may lead to extra visits to the outpatient clinic * Additional blood will be drawn when blood is already taken per standard of care * Bone marrow sampling at entry and at the end of the trial * MRI scans (or CT-scans) have to be performed * Quality-of-life questionnaires have to be filled out

NCT Number	NCT06605586
Lead Sponsor	Stichting Hemato-Oncologie voor Volwassenen Nederland
Conditions	Myelofibrosis
Enrollment	20 participants
Start Date	2025-02-20
Primary Completion	2027-12 (estimated)
Study Completion	2030-03 (estimated)
Updated on ClinicalTrials.gov	2025-03-07