Cancer patients monitored for years after experimental immune cell treatment
NCT ID NCT06701201
First seen Jun 27, 2026 · Last updated Aug 05, 2026 · Updated 2 times
Summary
This study follows 60 cancer patients who have already received SynKIR CAR T cell therapy to check for long-term side effects and see how well the treatment continues to work. Researchers will monitor for delayed reactions and measure survival over time. The goal is to understand the lasting safety and effectiveness of this personalized immune cell treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- SynKIR CAR T cells (immune cells engineered to target cancer)
- What this could lead to
- If successful, this study could show that SynKIR CAR T cell therapy is safe and effective over the long term for certain cancers.
- What could go wrong
- This is a long-term follow-up study, not a new treatment trial. It only includes people who already received the therapy, so results may not apply to new patients. Risks include delayed side effects.
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 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2025
- Expected to finish
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Feb 2042
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
Eligible participants must have received at least 1 infusion of a SynKIR CAR T cell product in a Verismo Therapeutics parent protocol.
- Ages
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18 years and older
- 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: Participants are eligible to be included in the study only if all of the following criteria apply: 1. All adult participants who have received any amount of SynKIR CAR T cell product in a study sponsored by Verismo Therapeutics. 2. Participant is willing and able to comply with the study requirements. Exclusion Criteria: There are no specific exclusion criteria.
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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
7 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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Colorado Blood Cancer Institute, part of Sarah Cannon Research Institute
Denver, Colorado, 80218, United States
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MD Anderson Cancer Center
Houston, Texas, 77030, United States
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Rutgers Cancer Institute
New Brunswick, New Jersey, 08901, United States
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University of Kansas Cancer Center
Westwood, Kansas, 66205, United States
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University of Pennsylvania Abramson Cancer Center
Philadelphia, Pennsylvania, 19104, United States
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University of Wisconsin Carbone Cancer Center
Madison, Wisconsin, 53792, United States
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Winship Cancer Institute of Emory University
Atlanta, Georgia, 30322, United States
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