Clinical Development ProgressThe Phase 1 dose-escalation study for CER-1236 moving into the next cohort indicates uninterrupted clinical advancement and continued evaluation in relapsed/refractory AML.
Clinical Safety ProfileNo safety issues reported so far with CER-1236 and one patient cleared for dose intensification, supporting a favorable early safety profile for the program.
Mechanism DifferentiationCER-1236's TIM-4–based design harnesses a natural immune/apoptosis pathway, creating a distinct approach that could reduce toxicities compared with traditional CAR-T therapies.