• Active Biotech has initiated patient enrollment in a Phase Ib/II clinical trial evaluating tasquinimod for myelofibrosis patients who are refractory or ineligible for JAK2 inhibitor treatment.
• The open-label study will assess tasquinimod's safety and efficacy as monotherapy, with a primary endpoint targeting 35% reduction in spleen volume after 24 weeks of treatment.
• The trial, sponsored by HOVON and financially supported by Oncode Institute, will be conducted across study centers in the Netherlands and Germany, addressing a significant unmet medical need.