Engineered immune cells take aim at Hard-to-Treat childhood leukemia
NCT ID NCT07695012
First seen Jul 10, 2026 · Last updated Jul 10, 2026
Summary
This trial investigates a personalized cell therapy called CAR-T for children and young adults (ages 5–50) with B-cell acute lymphoblastic leukemia that has relapsed or not responded to standard treatment. The therapy involves collecting a patient's own immune cells, engineering them to recognize and attack cancer cells, and infusing them back. The study aims to assess whether this approach is safe and feasible to manufacture locally, with a focus on monitoring side effects like cytokine release syndrome.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- Active substance
- CAR-T cell therapy (anti-CD19 chimeric antigen receptor T-cells)
- What this could lead to
- If successful, this approach could offer a new treatment option for patients whose leukemia has returned or not responded to standard therapies, potentially improving remission rates.
- What could go wrong
- This is an early-phase, small study (10 participants) focused on safety, so it may not show strong effectiveness. Risks include severe immune reactions like cytokine release syndrome (CRS) and neurological side effects.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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National University of Medical Sciences, Clinical Trial Unit
RECRUITINGRawalpindi, 46000, Pakistan
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact Phone: •••-•••-•••• Email: •••••@•••••
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