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Can engineered immune cells outsmart transplant-related cancer?

NCT ID NCT03131934

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Aug 07, 2026 · Last updated Aug 07, 2026

Summary

This early-phase trial tests a new type of immunotherapy for people who develop a rare blood cancer called post-transplant lymphoproliferative disease (PTLD) after a solid organ transplant. The treatment uses the patient's own immune cells (T-cells) that are engineered to resist the effects of tacrolimus, an immunosuppressant drug needed to prevent organ rejection. The goal is to see if these modified cells can safely fight the cancer while continuing to protect the transplanted organ. The trial compares the engineered cells to a control version to see which persists better in the body.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Autologous EBV-specific cytotoxic T-cells engineered to resist tacrolimus
What this could lead to
If successful, this approach could offer a targeted cellular therapy for post-transplant lymphoproliferative disease, potentially reducing the need for harsh immunosuppression reduction and improving outcomes.
What could go wrong
This is a very early, small phase 1 trial (only 4 participants), so safety and efficacy are far from proven. The engineered T-cells may not persist or control the disease, and there are risks of toxicity or graft rejection.

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.

Phase

Early phase 1

The earliest testing in people: a first look at safety, in a very small group.

Participants

4 people

The number who actually took part.

Started

May 2019

Finished

Mar 2026

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

1 year to 70 years

Sex

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. Adult and paediatric (age 1-70 years) solid organ transplant recipients with histologically proven B-lineage EBV+ post-transplant lymphoproliferative disease (PTLD) either de novo or resistant to Rituximab 2. EBV viraemia at enrolment 3. On immunosuppression with tacrolimus 4. Agreement to have a pregnancy test and use of contraception for duration of trial (if applicable) 5. Written informed consent Exclusion Criteria: 1. Fulminant disease 2. Requirement for supplemental oxygen 3. Burkitt's lymphoma/Mature B-acute lymphoblastic leukaemia with IgH-Myc rearrangement 4. T-lineage PTLD 5. Bilirubin \> 3 x upper limit of normal 6. Creatinine \> 3 x upper limit of normal 7. Active hepatitis B, C or HIV infection 8. Women who are pregnant or breast-feeding 9. ECOG performance score ≥ 4 10. Inability to tolerate leucapheresis

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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

  • Great Ormond Street Hospital

    London, United Kingdom

  • King's College Hospital

    London, United Kingdom

More trials for these conditions

Other studies related to the condition(s) this trial covers.