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TruGraf Liver Gene Expression Serial Test

StatusTerminated
PhaseNot specified
Started2024-08-01
View on ClinicalTrials.gov ↗
This is an Investigator Initiated, single center, non-randomized, single arm study utilizing TruGraf liver gene expression serial testing in patients with autoimmune liver diseases (AIH, PSC, PBC) monthly for the first 6 months after transplant to help inform immunosuppression (IS) optimization. Approximately 20 patients will be enrolled in the study. Study outcomes will include 1-year graft survival, 1 year BPAR and clinically treated rejection rates, number of changes to IS based on the results of Trugraf, eGFR and immune mediated issues. TruGraf®, (Transplant Genomics, Inc., a member of Eurofins Transplant Diagnostics) is a non-invasive blood-based test to assist the clinician in lowering immunosuppression in liver transplant patients. It is the first and only blood-based test that offers biomarker guidance to aid physicians in minimizing immunosuppression in transplant recipients. Unfortunately, achieving the tight control of therapeutic levels of immunosuppression that is required to maintain the balance between "too much" and "too little" can be difficult. TruGraf liver can help clinicians confirm immune "quiescence" prior to, as well as following, immunosuppression reduction in patients with stable graft function, minimizing the risk of overt graft injury due to rejection. The clinical context of use for TruGraf is to provide reassurance to the clinician who is contemplating a preemptive reduction in IS therapy that a patient's immune status is "quiescent" thus reducing the risk of triggering acute rejection with that IS reduction. Having the ability to assess whether the patient's immune status is "quiescent" or activated when considering an increase or decrease in IS therapy allows the clinician greater confidence in decision making.

Amendment history 5 changes detected by DataLookout

2026-08-08
critical
Trial status changed: Enrolling by Invitation → Terminated
2026-08-08
critical
Trial terminated: Funding discontinued
2026-08-08
critical
Enrollment reduced: 20 → 13 participants
2026-08-08
minor
Primary completion pushed: 2025-11 → 2025-12-03
2026-08-08
minor
Completion moved earlier: 2026-12 → 2025-12-03
Trial Details
NCT Number NCT06061341
Lead Sponsor Washington University School of Medicine
Collaborators: Transplant Genomics, Inc.
Conditions Autoimmune Liver Disease, Autoimmune Hepatitis, Primary Sclerosing Cholangitis, Primary Biliary Cirrhosis
Enrollment 13 participants
Start Date 2024-08-01
Primary Completion 2025-12-03 (estimated)
Study Completion 2025-12-03 (estimated)
Updated on ClinicalTrials.gov 2026-08-07