Engineered t cells take on deadly childhood brain cancer

NCT ID NCT05478837

First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This early-phase trial tests a new treatment for children and young adults with a rare, aggressive brain tumor called H3.3K27M-mutated diffuse midline glioma. The treatment involves taking a patient's own immune cells (T cells), genetically modifying them in the lab to recognize the tumor, and giving them back after a short course of chemotherapy. The main goals are to see if the treatment is safe and to find the best dose.

What this could mean

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

Active substance

genetically modified T cells (KIND T cells) plus chemotherapy (cyclophosphamide and fludarabine)

What this could lead to

If it works, this could point toward a new treatment option for a rare and aggressive brain tumor that currently has few effective therapies.

What could go wrong

This is a very early, small phase 1 trial with only 12 participants, so it is primarily testing safety and dosing. The treatment may not shrink tumors or improve survival, and there are risks from the chemotherapy and the modified cells themselves.

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.

diffuse midline glioma, H3 K27M-mutant

As listed by the trial registrant

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

Contacts and locations

Locations

  • University of California, San Francisco

    San Francisco, California, 94143, United States