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Recruiting Phase 1, Phase 2 NCT07269041

Immune Tolerance Induction After Liver Transplantation

Trial Parameters

Condition Liver Transplantation
Sponsor University of California, Los Angeles
Study Type INTERVENTIONAL
Phase Phase 1, Phase 2
Enrollment 12
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2026-02-20
Completion 2029-01
Interventions
Donor Hematopoietic Stem and Progenitor Cell Infusion

Brief Summary

This clinical trial is being conducted to help liver transplant recipients safely discontinue toxic immunosuppressive drugs years after surgery. Lifelong use of these drugs is the current standard, but they come with life-threatening side effects. UCLA has pioneered this "Delayed Tolerance" approach, achieving success in numerous kidney recipients now living drug-free. The process uses a conditioning regimen followed by donor stem cell infusion to retrain the immune system to accept the liver as "self."

Eligibility Criteria

Recipient Inclusion Criteria: 1. Males and females ages 18 years and older with a pre-existing liver transplant from a living donor with a donor-recipient match at 6 or more out of 12 alleles across the HLA-A, -B, -C, -DR, -DQ, and -DP loci, as determined by high-resolution HLA typing. 2. Pre-existing living-donor liver transplant must be 12 months to 20 years from date of scheduled HSPC infusion. 3. Agreement to participate in the study and ability to give informed consent. 4. Liver biopsy within 4 weeks of enrollment without signs of rejection. 5. Meets institutional criteria for HSPC infusion. 6. Resides or is willing to stay within 3 hours distance from UCLA Medical Center by ground transportation for the first three months of the trial at the physician's discretion. 7. No known contraindication to administration of rATG or radiation therapy. 8. If subject is a female of reproductive potential (i.e., no documented absence of ovaries or uterus, history of tubal ligation, or post-men

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