Clinical Trial SuccessThe trial met its primary endpoint of 6-month durable complete remission (dCR), as well as its secondaries.
Pipeline AdvancementPositive data from the completed P1b combination trial of Actimab-A + CLAG-M showed high rates of response, measurable residual disease negativity, bone marrow transplant access, and improved survival outcomes in high-risk patients.
Regulatory ProgressActinium announced FDA clearance for an IND to study Iomab-ACT as targeted conditioning before CAR-T therapy and for BMT for sickle cell patients.