Engineered immune cells take aim at stubborn leukemia

NCT ID NCT05995041

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This phase 1 trial tests a new type of immunotherapy called universal CAR T cells in people with acute myeloid leukemia (AML) that has come back or not responded to treatment. The cells are engineered to recognize and attack leukemia cells by targeting four different proteins (CLL-1, CD33, CD38, and CD123). The study aims to see if this treatment is safe and whether it can shrink tumors or lead to remission.

What this could mean

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

Active substance

universal CAR T cells targeting CLL-1, CD33, CD38, and CD123

What this could lead to

If successful, this approach could offer a new treatment option for patients with hard-to-treat acute myeloid leukemia, potentially improving remission rates.

What could go wrong

This is an early phase 1 trial with a small number of participants, so safety and effectiveness are not yet proven. CAR T cell therapy can cause severe side effects like cytokine release syndrome.

Disclaimer Read more

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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Conditions

The condition(s) this trial relates to.

acute myeloid leukemia

As listed by the trial registrant

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

Contacts and locations

Study contacts

  • Contact

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

  • Contact

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

Locations

  • Shenzhen Geno-Immune Medical Institute

    RECRUITING

    Shenzhen, Guangdong, 518000, China

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