Engineered immune cells under Long-Term watch: will the benefits last?
NCT ID NCT07683897
First seen Jul 06, 2026 · Last updated Jul 31, 2026 · Updated 3 times
Summary
This study follows people who have already been treated with Senza5 CART5, a personalized cell therapy that uses a patient's own immune cells engineered to target cancer. The goal is to track long-term safety and how well the treatment continues to control the disease. Participants will be monitored for any side effects related to the therapy over time.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Senza5 CART5 (a type of engineered immune cell therapy)
- What this could lead to
- If successful, this follow-up could show that Senza5 CART5 provides lasting disease control with an acceptable long-term safety profile.
- What could go wrong
- This is a small, non-randomized follow-up study, so results may not apply to all patients. Long-term side effects or loss of effectiveness are possible.
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 30 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Jul 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 treated with Senza5 CART5 who have met all eligibility criteria and provided written informed consent for LTFU-Viper 101 (or have written informed consent from their parent\[s\]/legal guardian\[s\] and have provided assent, as applicable).
- Ages
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18 to 100 years
- Sex
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Anyone
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 meeting the following criteria are eligible for trial participation: * Provision of written informed consent by the participant or provision of written informed consent from the participant's parent\[s\]/legal guardian\[s\] and provision of assent from the participant, as applicable * Treated with Senza5 CART5 in a Vittoria BioTherapeutics sponsored clinical trial * Able to comply with trial requirements Exclusion Criteria: * There are no exclusion criteria.
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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 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.