A Study Of Biomarkers To Optimize Immunosuppression Late Post-Liver Transplant

Overview

About this study

The purpose of this study is to determine the safety and feasibility of a clinical protocol using transplant rejection biomarkers to reduce immunosuppression late post-liver transplant.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

Participants must meet all of the below inclusion criteria in order to participate in this study:

  • ≥ 18 years of age at the time of transplant.

  • First or subsequent liver transplant from a deceased (DBD or DCD) or living donor.

 Exclusion Criteria: 

Candidates meeting any of the below exclusion criteria will be excluded from study participation.

  • Recipient of a multiorgan transplant.

  • History of a non-liver solid organ transplant, bone marrow transplant, hemopoietic stem cell transplant, or islet cell transplant.

  • Inability or unwillingness of individual or legal guardian/representative to give written informed consent.

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 6/09/2025. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Rochester, Minn.

Mayo Clinic principal investigator

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Scottsdale/Phoenix, Ariz.

Mayo Clinic principal investigator

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Jacksonville, Fla.

Mayo Clinic principal investigator

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More information

Publications

Publications are currently not available
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CLS-20598352

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