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Immune Tolerance Induction After Liver Transplantation

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

Condition(s)Liver Transplantation, Immune Tolerance, Immune Tolerance/Drug Effects, Graft Survival, Hematopoietic Stem Cell, Chimerism, Immunosuppression After Liver Transplantation, Immunosuppression Disorders,
StatusRecruiting
PhasePhase 1, Phase 2
Study typeInterventional
SummaryThis 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."
Who can participateRecipient 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 contra
Ages18 Years
SexAll
Lead sponsorUniversity of California, Los Angeles
LocationsLos Angeles, California, United States
Start date2026-02-20
NCT IDNCT07269041
Official listinghttps://clinicaltrials.gov/study/NCT07269041

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