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NCT Number: NCT06557564

Diagnosis of Graft Pathology by TruGraf

The goal of this observational study is to to identify different causes of liver diseases or damage in liver transplant patients and develop a machine learning algorithm as a non-invasive tool leveraging gene expression and patient clinical information to classify transplant liver diseases We will collect blood samples of the participants who had undergone or will undergo the liver biopsy as part of standard of care, and use this blood in TruGarf. TruGraf is a non-invasive test that measures differentially expressed genes in the blood of transplant recipients to rule out liver damage. Researcher will collect the biopsy result from the medical record and this will be compared with the TruGarf results.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Toronto General Hospital -UHN

Toronto, Ontario, M5G 2N2, Canada

Location status: Recruiting

Location contact

Mamatha Bhat, MD

PRINCIPAL_INVESTIGATOR

Sameera Rizvi

CONTACT

[email protected]

416-340-4800 ext. 4878

About this study

Given the significant investment of healthcare resources into transplantation, it is critical to identify recipients with graft pathologies such as Acute Cellular Rejection (ACR), NASH, cholestasis, etc. at an earlier stage to implement the appropriate intervention, rather than initiating empiric treatment that could be unsafe. This project will develop a practical Machine learning-based tool based on the results of the TruGraf assay alongside clinical and laboratory data for non-invasive diagnosis of graft pathology. TruGraf is a non-invasive test that measures differentially expressed genes in the blood of transplant recipients to identify patients who are likely to be adequately immunosuppressed and, in doing so, rule out graft damage. TruGraf measures the difference in gene expression for a precise panel of specific genes that have been empirically determined to discriminate between allografts that are truly healthy (Non-ACR), and those in transplant patients that have acute rejection on biopsy (AR). Nevertheless, the exact etiology of graft damage may be difficult to discern for the transplant clinician. The clinical characteristics and history of the liver transplant recipient as well as liver enzyme patterns can provide a pre-test probability of one diagnosis being more likely than the other (Acute cellular rejection, NASH, biliary or viral disease). The proposed tool will leverage our expertise in Machine Learning tools applied to clinical and molecular data (TruGraf assay results) to enable effective clinical implementation of the TruGraf assay.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • . Single-organ Liver transplant recipients
  • Male or female, age > 18 years at the time of signing informed consent.
  • Willing and able to provide informed consent.
  • Patients will be undergoing liver graft biopsy (for any reason), or have had a liver biopsy within 48 hours of consent.

Exclusion criteria

  • Repeat transplant
  • Recipient of multi organ transplantation
  • Any treatment for graft rejection such as IV steroids has been given before biopsy.
  • Targeted biopsies for diagnosis of malignancy.

Treatment and study plan

TruGraf liver gene expression

Genetic

Blood from the patients undergoing graft liver biopsy will be collected on the day of the liver biopsy, preferable prior to tissue collection or within 48 hours following the biopsy. Two specialized PaxGene tubes containing 2.5mL of blood each will be filled and will be sent to TGI laboratory in USA for processing, storage, and analysis using TGI's proprietary bioinformatics TruGraf will provide UHN with a Liver binary result: ACR or non-ACR. The results data will be batched and sent to UHN at agreed upon timepoints.

Primary outcomes

  1. Develop and validate a ML-based algorithm

    Time frame: 36 months

    Develop and validate a ML-based algorithm that identifies major graft pathologies using liver biopsy as the reference method.

Secondary outcomes

  1. Identify specific etiologies of ongoing graft damage

    Time frame: 36 months

    Identify specific etiologies of ongoing graft damage by examining TruGraf gene expression array.

Study contacts

Contact information is provided by the study sponsor or research team.

Sameera Rizvi

CONTACT

[email protected]

4163404800 ext. 4878

Sponsors and collaborators

Lead sponsor

University Health Network, Toronto

Other

Collaborators

  • Transplant Genomics, Inc.

Registry information

Official study title

Development of a Machine Learning Tool for Non-invasive Diagnosis of Liver Graft Pathology Using TruGraf

Important dates

Study start
2024
Primary completion
2027
Study completion
2027
First posted
Aug 16, 2024
Registry last updated
Aug 16, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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