TLI- and ATG-Enabled Minimization Protocol in Liver Transplantation

ConditionLiver Failure
Trial statusRecruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age18-55
SponsorStanford University

About this trial

The unmet medical need in solid organ transplantation is to eliminate the lifelong requirement of powerful immune suppression drug combinations with their attendant side effects, and to prevent immune mediated rejection of the organ transplant. The proposed trial is designed to study if following a 'standard of care' deceased donor liver transplant host conditioning using Total Lymphoid Irradiation (TLI) and Anti-Tthymocyte Globulin (ATG) will result in operational tolerance and ultimately allow for immunosuppression drug minimization or cessation.

It has been hypothesized that the ATG and TLI conditioning regimen post liver transplant will be safe and well tolerated and will result in recipients successfully being withdrawn from immunosuppression within 2 years after liver transplantation. We will test the hypothesis that by using a conditioning regimen of ATG and TLI to induce this operational tolerance will allow immunosuppressive drug minimization and cessation while maintaining normal graft function and without the risk of graft rejection.

Importance of this knowledge:

Operational tolerance occurs spontaneously in a minority of liver transplant recipients; however, predictable and reproducible induction of tolerance remains an unmet need. Building on extensive experience with TLI-based tolerance induction in kidney transplantation at Stanford, this study aims to evaluate whether a non-myeloablative conditioning regimen using TLI and ATG can safely facilitate immunosuppression minimization and withdrawal in liver transplant recipients without the use of donor hematopoietic cell infusion.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Undergoing liver transplantation at Stanford University

No contraindications to Total Lymphoid Irradiation or rabbit antithymocyte globulin (rATG)

Disqualifiers

Contraindications to Total Lymphoid Irradiation (e.g. pregnancy, bone marrow suppression or disease, autoimmune disease, prior radiation in the field)

Contraindications to rATG

Patients with history of hepatocellular carcinoma (HCC) or other malignancies with exception of non melanoma skin cancer in remission

Model of End-Stage Liver Disease (MELD) score > 25

Trial design

Design model

Parallel

Treatments tested in this trial

  • Anti-Thymocyte Globulin, ATG (Rabbit)

    Drug

    1.5 mg/kg ATG will be administered intravenously over 3-4 days. The ATG doses will be completed within 5 days of the liver transplant.

  • Total lymphoid irradiation

    Device

    Participants will get 8 doses of TLI over 2 weeks with a total radiation dose of 960 cGy.

Treatment groups

12 Participants
are divided into 2 treatment groups
Group A: Anti-thymocyte globulin and Total Lymphoid Irradiation (synchronous tolerance)Experimental treatment 2 interventions
Group B: Anti-thymocyte globulin and Total Lymphoid Irradiation (delayed tolerance)Experimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

The success rate

The success rate is defined as the percentage of participants free from all immunosuppressive drugs by 18 months after the start of the conditioning regimen). This will be estimated with standard errors by the Kaplan-Meier procedure and the Greenwood formula.

Time frame
After intervention through 18 months and monitored monthly up to 36 months.

Secondary outcomes

Other outcomes

Sponsors and contacts

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