Plain-English translation of NCT04881240 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
Phase 1 — Testing in a small group (usually 20–80 people) to find a safe dose and watch for side effects.
This is a Phase I study testing allogeneic memory T-cell therapy—immune cells taken from a healthy family member, engineered in a lab to recognize and fight leukemia cells, and then given to a young patient. The trial is designed to find the safest dose and evaluate how well this treatment works in children and young adults up to age 21 whose leukemia has returned or is no longer responding to standard therapies.
Many children with relapsed or refractory leukemia don't have good treatment options left. Some cannot receive the standard engineered cell therapy (called autologous CAR T-cell therapy) because they're too young, too small, or their disease is growing too fast. This new treatment uses cells from a matched family member instead, offering hope to patients who might otherwise have no options.
You likely qualify if…
You likely don't qualify if…
You and your matched family member will both be part of the study. Your family member will undergo a procedure called apheresis to collect immune cells, which are then sent to a laboratory where they are engineered to recognize your leukemia cells. After the cells are manufactured, you will receive them as an infusion. The study includes careful monitoring through clinic visits to watch for side effects and to see how well the treatment is working. The exact number and timing of visits will depend on your health and how you respond to the treatment.
AI-generated summary from trial data · Jun 30, 2026 · Not medical advice
United States