Engineered immune cells take aim at returning leukemia

NCT ID NCT03326921

First seen Nov 15, 2025 · Last updated Jun 20, 2026 · Updated 27 times

Summary

This early-phase trial tests a new type of immunotherapy for children and adults whose acute leukemia has come back or not responded after a donor stem cell transplant. The treatment uses specially engineered donor immune cells (T cells) that are designed to recognize and attack a protein called HA-1 found on leukemia cells. The study will enroll 24 participants to find the safest dose and see if the cells can be successfully made and given.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

  • Contact

    Phone: •••-•••-••••

Locations

  • Fred Hutch/University of Washington Cancer Consortium

    RECRUITING

    Seattle, Washington, 98109, United States

    Contact

    Contact Phone: •••-•••-•••• Email: •••••@•••••

    Contact Phone: •••-•••-••••

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

HA-1-specific T cells (immune cells engineered to recognize and attack leukemia cells)

What this could lead to

If successful, this could offer a new treatment option for leukemia that returns after a stem cell transplant, potentially improving outcomes for patients with limited alternatives.

What could go wrong

This is an early phase 1 trial with only 24 participants, so safety and dosing are still being evaluated. The therapy may not work for everyone, and there are risks of side effects like graft-versus-host disease or immune reactions.

Conditions

The condition(s) this trial relates to.

acute biphenotypic leukemia acute lymphoblastic leukemia acute myeloid leukemia blast phase chronic myelogenous leukemia, BCR-ABL1 positive Blastic Plasmacytoid Dendritic Cell Neoplasm childhood acute myeloid leukemia chronic myelomonocytic leukemia juvenile myelomonocytic leukemia leukemia Leukemia, Myelogenous, Chronic, BCR-ABL Positive myelodysplastic syndrome Myelodysplastic Syndromes Neoplasm, Residual Precursor Cell Lymphoblastic Leukemia-Lymphoma

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.