CAR-T therapy patients monitored for years in new safety study
NCT ID NCT07474051
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study follows 178 patients who previously received an AvenCell CAR-T cell therapy for cancers like lymphoma, leukemia, or prostate cancer. Researchers will track delayed side effects, including new cancers or autoimmune issues, for years. No new treatment is given—this is purely a long-term safety check.
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 (UniCAR or RevCAR platforms)
- What this could lead to
- If successful, this study could provide crucial safety data to support the broader use of these CAR-T therapies.
- What could go wrong
- This is a long-term follow-up study, not a treatment trial. It cannot prove the therapy works, and results depend on patient participation and data quality.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 178 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2026
- Expected to finish
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Jan 2041
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Participants Who Received an AvenCell CAR-T Cell Therapy
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Participant who received an AVC-CAR-T cell therapy within an AVC-sponsored clinical trial. 2. Participant signed written informed consent for the AVC-PERSIST study. Exclusion Criteria: 1. Participant is unable to provide written informed consent. 2. Participant is unable to comply with study requirements in the eyes of the Investigator.
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Get notified about this study
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
5 sites. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Charité Universitätsmedizin Berlin
Berlin, Germany
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Klinikum der Universität (LMU) Muenchen
Munich, Germany
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Technische Universitaet Dresden - Universitaetsklinikum Carl Gustav Carus
Dresden, Germany
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Universitatsklinikum Ulm
Ulm, Germany
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Universitätsklinikum Marburg
Marburg, Germany
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- New PET tracer aims to light up hidden cancer targets
- Can daily adaptive radiotherapy spare healthy tissue in prostate cancer?
- Can a radioactive tracer and MRI reveal prostate Cancer's true extent?
- Five-Fraction radiation plus hormone therapy tested against High-Risk prostate cancer
- Can regional data improve bone marrow transplant results for blood cancers?