15-Year watch begins for experimental transplant therapy
NCT ID NCT05987527
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study follows 11 kidney transplant patients who received an experimental cell therapy called TX200-TR101 in an earlier trial. Researchers will monitor them for up to 15 years to check for long-term side effects and how well their transplanted kidney is doing. The goal is to see if this personalized therapy is safe 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
- TX200-TR101 (a personalized cell therapy using the patient's own modified immune cells)
- What this could lead to
- If successful, this could show that TX200-TR101 is safe over many years and may help reduce the need for lifelong anti-rejection drugs in kidney transplant patients.
- What could go wrong
- This is a small, early follow-up study (only 11 people) and does not test whether the therapy works. Long-term risks or side effects may still emerge.
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
-
About 11 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Aug 2023
- Expected to finish
-
Jun 2039
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
Transplant recipients enrolled in the Phase I/IIa study (TX200-KT02) and who have consented to participate in this LTFU study,
- Ages
-
18 to 72 years
- Sex
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Anyone
- Healthy volunteers
-
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. Subjects who enrolled in the Phase I/IIa study TX200-KT02, received a transplanted kidney and have either completed or withdrawn from that study. 2. Willing and able to provide written informed consent (IC) in accordance with local regulations and governing Independent Ethics Committee (IEC)/Institutional Review Board (IRB) requirements prior to any procedure or evaluation performed specifically for the sole purpose of the study. Exclusion Criteria: * N/A
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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
-
Erasmus MC, University Medical Center
Rotterdam, Netherlands
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Leiden University Medical Centre
Leiden, Netherlands
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Oxford University Hospitals NHS Foundation Trust
Oxford, United Kingdom
-
University Hospitals Leuven
Leuven, Belgium
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University Medical Center Groningen
Groningen, Netherlands
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