Gene therapy trial targets tough T-Cell cancers
NCT ID NCT07055477
First seen Jun 25, 2026 · Last updated Jul 17, 2026 · Updated 2 times
Summary
This early-stage trial tests a new gene therapy for certain T-cell lymphomas that have come back or not responded to treatment. The therapy uses a patient's own white blood cells, modified to attack cancer cells that carry a protein called CCR4. Up to 60 adults will receive the modified cells after chemotherapy, and researchers will monitor safety and side effects for up to 15 years.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- Active substance
- CCR4 CAR T cells (a type of gene therapy using the patient's own immune cells)
- What this could lead to
- If it works, this could lead to a new treatment option for people with hard-to-treat T-cell lymphomas.
- What could go wrong
- This is an early phase 1 trial with only 60 participants, focused on safety. It may not work for everyone, and side effects could be serious.
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
Locations
-
National Institutes of Health Clinical Center
RECRUITINGBethesda, Maryland, 20892, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can a targeted pill boost Chemo's power against a rare blood cancer?