Liver TransplantPhase 2OPTIMALNCT02533180
Evaluation of Donor Specific Immune Senescence and Exhaustion as Biomarkers of Tolerance Post Liver Transplantation
A Phase 2 study testing Immunosuppression withdrawal in people with Liver Transplant and Liver Transplantation, run by National Institute of Allergy and Infectious Diseases (NIAID) at 7 sites in United States.
Trial summary
The primary aim of this study is to determine whether a peripheral blood or graft lymphocyte phenotype of immune senescence or exhaustion is different between operationally tolerant and non-tolerant liver allograft recipients. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Liver Transplant, Liver Transplantation
- What is being tested?
- Immunosuppression withdrawal
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 100 participants
- Where
- 7 sitesUnited States
- Study dates
- 15 Dec 2015to 8 Jul 2022
- Phase
- Phase 2
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Recipient participants must meet all of the following criteria to be eligible for this study:
- At the time of screening:
- 18 to 50 years old and more than 6 years post-transplant OR
- Greater than 50 years old and more than 3 years post-transplant
- Recipient of either deceased or living donor liver transplant. Recipients of living donor transplants must have a donor who is also willing to enroll
- Recipient of single organ transplant only
Show all 22Show fewer
- Must have a screening liver biopsy that fulfills the following criteria based on the central pathology reading:
- Portal inflammation and interface activity is preferably absent, but minimal to focal mild portal mononuclear inflammation may be present. Interface necro-inflammatory activity is absent or equivocal/minimal and, if present, involves a minority of portal tracts and not generally associated with fibrosis
- Negative for perivenular inflammation
- Lymphocytic bile duct damage, ductopenia, and biliary epithelial senescence changes are absent unless there is an alternative, non-immunological explanation (e.g. biliary strictures)
- Fibrosis (if present) should be mild overall, and portal-to-portal bridging should not be more than rare. Perivenular and peri-sinusoidal fibrosis should not be more than mild according to the Banff criteria
- Findings for obliterative or foam cell arteriopathy are negative
- Liver function tests (Direct bilirubin, alanine aminotransferase (ALT)), less than twice the upper limit of normal (ULN). ULN values for liver function tests will be defined by ranges from Harrison's Principles of Internal Medicine, 18th edition
- Receiving calcineurin inhibitor (CNI) based maintenance immunosuppression. Participants may also concurrently receive:
- Low dose mycophenolate mofetil (MMF ≤ 1500 mg daily) or mycophenolic acid (≤ 1080 mg daily), OR
- Prednisone ≤ 7.5 mg daily, or equivalent corticosteroid
- Ability to sign informed consent
- Living donor participants must meet all of the following criteria to be eligible for this study:
- At the time of screening: ≥18 years old
- Living donor of the liver allograft of an enrolled recipient participant
- Ability to sign informed consent
- Willingness to donate appropriate biologic samples
Who cannot join
- Recipient participants who meet any of the following criteria will not be eligible for this study:
- History of hepatitis C virus (HCV) infection (defined as a positive HCV antibody test)
- Positive antigen-antibody immunoassay for human immunodeficiency virus, HIV-1/2
- Serum positivity for HBV surface antigen or HBV-DNA
- History of immune-mediated liver disease in which immunosuppression discontinuation is inadvisable (autoimmune hepatitis, primary sclerosing cholangitis, primary biliary cirrhosis)
- Any medical condition associated with a likely need for systemic corticosteroid administration, e.g., reactive airways disease
Show all 22Show fewer
- Prospective baseline liver biopsy showing any of the following: (see recipient inclusion criteria #4)
- acute rejection according to the Banff global assessment criteria
- early or late chronic rejection according to the Banff global assessment criteria
- inflammatory activity and/or fibrosis in excess of permissive criteria according to Banff 2012 criteria
- any other histological findings that might make participation in the trial unsafe. Eligibility will be determined by the findings on the central biopsy reading
- Rejection within the 52 weeks prior to screening
- Estimated glomerular filtration rate (GFR) <40 ml/min as calculated by CKD-EPI method (to mitigate the risk of worsening renal failure should rejection occur and high level of CNI be required)
- The need for chronic anti-coagulation that cannot be safely discontinued for a minimum of 1 week to safely perform a liver biopsy
- Pregnant females and females of childbearing age who are not using an effective method of birth control
- Current drug or alcohol dependency
- Inability to comply with the study visit schedule and required assessments, including frequent liver function monitoring and protocol biopsies
- Inability to comply with study directed treatment
- Any medical condition that in the opinion of the principal investigator would interfere with safe completion of the trial
- Participation in another interventional clinical trial within the 4 weeks prior to screening
- Living donor participants who meet any of the following criteria will not be eligible for this study:
- 1. Any medical condition, such as anemia, coagulopathy, etc., that in the opinion of the principal investigator would interfere with safe participation in the trial
Trial locations and contacts
7 sites in 1 country.
7 sites in 1 country
United States7 sites
Massachusetts General Hospital
Boston, Massachusetts, 02114
Northwestern University Feinberg School of Medicine
Chicago, Illinois, 60611
Baylor University Medical Center at Dallas
Dallas, Texas, 75246
Columbia University Medical Center
New York, New York, 10032
Hospital of the University of Pennsylvania
Philadelphia, Pennsylvania, 19104
University of Pittsburgh Medical Center
Pittsburgh, Pennsylvania, 15213
University of California, San Francisco Medical Center
San Francisco, California, 94143
About this study
Official title: Evaluation of Donor Specific Immune Senescence and Exhaustion as Biomarkers of Operational Tolerance Following Liver Transplantation in Adults (ITN056ST)
The primary aim of this study is to determine whether a peripheral blood or graft lymphocyte phenotype of immune senescence or exhaustion is different between operationally tolerant and non-tolerant liver allograft recipients.
Read the detailed description
People who have liver transplants must take anti-rejection medication (immunosuppression) for the rest of their lives. If they stop, their immune system may reject the transplanted liver. All anti-rejection medications have side effects. Because of the side effects of anti-rejection medications, an important goal of transplant research is to allow people to accept their transplanted organ without long term use of anti-rejection medications. This is called tolerance. In this study, participants who received a liver transplant will have their anti-rejection medication(s) gradually reduced over a period of time and then stopped. The study calls this 'immunosuppression withdrawal'.
The purpose of this research study is to see how many people will develop tolerance after immunosuppression withdrawal. The researchers also want to find out if there are blood or liver biopsy tests that can help transplant doctors in the future predict whether it is safe to decrease or stop anti-rejection medications in people who received a liver transplant.
- Conditions
- Liver Transplant, Liver Transplantation
- Being tested
- Immunosuppression withdrawal
- Keywords
- Liver allograft recipient, Immunosuppression withdrawal, Calcineurin inhibitor (CNI) based immunosuppression, Living Donor (of the Respective Liver Transplant Recipient)
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Immunosuppression withdrawalBiological
Also called ISW
Participants will initiate calcineurin inhibitor (CNI) withdrawal after at least 3 weeks of stable liver function, as documented by liver function tests (direct bilirubin, alanine aminotransferase and gamma-glutamyl transferase) separated by at least 1 week in the 3 week period prior to withdrawal.
CNI withdrawal will occur in eight 3 week intervals with each subsequent reduction based on liver function tests over the prior 3 week interval.
Participants on CNI and prednisone will undergo withdrawal from the two therapies concurrently.
If participants are weaned off the CNI successfully, they will initiate non-CNI withdrawal. The non-CNI withdrawal includes two dose reductions of approximately 50% over a 6 week period each, after which the drug will be discontinued.
| Study group | Role | What they receive |
|---|---|---|
| Immunosuppression withdrawal (ISW) | Other | Gradual immunosuppression withdrawal according to the protocol defined algorithm Receives: Biological: Immunosuppression withdrawal |
What is being measured
The primary outcome is the main question the study is designed to answer.
The Percent of Participants Who Achieve Operational Tolerance 52 Weeks After Completion of Immunosuppression Withdrawal.
Participants are considered as successfully withdrawn from immunosuppression if they remain off immunosuppression for at least 52 weeks without evidence of rejection since enrollment and have a liver biopsy at 52 weeks following completion of immunosuppression withdrawal demonstrating histological stability and the absence of rejection per Banff global assessment criteria. This biopsy is assessed by the central pathologist. All participants who fail to complete immunosuppression withdrawal, regardless of reason, or fail to have a biopsy 52 weeks after completion of immunosuppression withdrawal will be considered to have failed.
Measured: From initiation of immunosuppression withdrawal through 52 weeks after stopping all immunosuppression
Secondary outcomes (15)
Proportion of Participants Who Develop Donor-Specific AlloAbs (DSA) or de Novo Anti-human Leukocyte Antigen Human Leukocyte Antigen (HLA) Antibodies
HLA is a molecule formed by a complex of genes which encode cell-surface proteins responsible for the regulation of the immune system. This molecule is unique for each individual. HLA molecules are present in all cells and are responsible for helping the immune system distinguish between your own cells and foreign cells (like pathogens). However, when our immune system encounters HLA molecules from another individual (like during pregnancy, after blood transfusions or transplantation) it recognizes this as foreign and can generate anti-HLA antibodies. These anti-HLA antibodies could cause harm to the transplanted organ by recognizing its cells as foreign triggering the immune system to attack. This endpoint looks at the development of newly developed donor-specific antibodies (DSA). DSA are a subset of anti-HLA antibodies that are specific against the donor organ. These anti-HLA antibodies are categorized into two classes-class I and class II. The data shown is only for class II DSA.
Measured: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
The Incidence of Acute Rejection, Steroid Resistant Rejection, and Chronic Rejection
Incidence will be measured as the proportion of participants who have acute rejection (per Banff criteria), steroid resistant rejection (rejection requiring antibody treatment), and chronic rejection (per Banff criteria), separately. The endpoint is summarized with a two-sided, 95% exact binomial confidence interval.
Measured: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
The Severity of Acute Rejection, Steroid Resistant Rejection, and Chronic Rejection
Severity is based on the Banff global assessment grade according to the central pathology reading of the liver biopsy. For an individual subject, the worst severity is reported. Acute rejection is categorized into mild (rejection infiltrate in a minority of triads that is generally mild and confined within the portal spaces), moderate (rejection infiltrate expanding most or all of the triads), or severe (rejection infiltrate expanding most or all of the triads with spillover into periportal areas and moderate to severe perivenular inflammation that extends into the hepatic parenchyma and is associated with perivenular hepatocyte necrosis). Chronic rejection is categorized into early (bile duct atrophy/loss and foam cell obliterative arteriopathy in <50% of the portal tracts) or late (early criteria but >50% of the portal tracts) stage. Steroid resistant rejection is always considered severe. The endpoint is summarized with a two-sided, 95% exact binomial confidence interval.
Measured: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
The Timing of Acute Rejection, Steroid Resistant Rejection, and Chronic Rejection
Time is measured as the time (in days) from the initiation of immunosuppression withdrawal to the time of the first biopsy showing rejection (per Banff criteria).
Measured: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
The Incidence of Graft Fibrosis in Tolerant Versus Non- Tolerant Patients.
Fibrosis of the liver is the formation of an excessive accumulation of scar tissue in the liver. Graft fibrosis was measured two ways by the ISHAK scale and by Liver Allograft Fibrosis Score (LAFSc) via a liver biopsy. Both scales range from 0 to 6, with a higher score indicating more severe fibrosis. A subject is considered as having graft fibrosis if the score is greater than or equal to 2 at their last available biopsy after the initiation of immunosuppression withdrawal.
Measured: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
The Progression of Graft Fibrosis in Tolerant Versus Non- Tolerant Patients
Fibrosis of the liver is the formation of an excessive accumulation of scar tissue in the liver. Graft fibrosis was measured two ways by the ISHAK scale and by Liver Allograft Fibrosis Score (LAFSc) via a liver biopsy. Both scales range from 0 to 6, with a higher score indicating more severe fibrosis. Progression was calculated as the final available biopsy score minus the baseline biopsy score. A positive value indicates a worsening of fibrosis.
Measured: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
The Incidence of Graft Loss
A participant is considered to have graft loss when the donated liver needs to be removed and the participant is retransplanted with another donor liver or the participant is listed for retransplant. The endpoint will be summarized with a two-sided, 95% exact binomial confidence interval.
Measured: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
The Incidence of All-Cause Mortality
This number reflects all deaths observed in all participants in the study period, regardless of the cause. The endpoint will be summarized with a two-sided, 95% exact binomial confidence interval.
Measured: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
The Incidence of Study-related SAEs
An adverse event is considered a serious adverse event (SAE) if it results it any one of the following: death, life-threatening, inpatient hospitalization or prolongation of existing hospitalization, persistent or significant incapacity or substation disruption to conduct normal life functions, congenital anomaly or birth defect, or an important medical event. The event is considered study related if the medical monitor deems it to be at least possibly or definitely related to any of the study interventions/procedures (immunosuppression withdrawal, the blood draw, or the liver biopsy). The endpoint will be summarized with a two-sided, 95% exact binomial confidence interval.
Measured: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
The Proportion of Operationally Tolerant Subjects Who Remain Free of Rejection at 3 Years After Completing Immunosuppression Withdrawal.
Participants are considered operationally tolerant if they remain off immunosuppression for at least 52 weeks without evidence of rejection since enrollment and have a liver biopsy at 52 weeks following completion of immunosuppression withdrawal demonstrating histological stability and the absence of rejection per Banff global assessment criteria (as assessed by the central pathologist). This number reflects the participants that continue to show the absence of rejection per the Banff global assessment criteria (as assessed by the central pathologist) in the 3 years following completion of immunosuppression withdrawal. The endpoint will be summarized with a two-sided, 95% exact binomial confidence interval.
Measured: From initiation of immunosuppression withdrawal through 3 years after completing immunosuppression withdrawal.
Changes in Renal Function (Defined as Estimated GFR Calculated by the CKD-EPI Creatine Equation 2021) in Tolerant Versus Non-tolerant Participants at 1, 2 and 3 Years After Completing Immunosuppression Withdrawal.
Glomerular filtration rate (GFR) is a measure of kidney function and helps determine the stage of kidney disease. A value less than 15 indicates kidney failure, 15 to 29 indicates severe loss of kidney function, 30 to 44 indicates moderate to severe loss of kidney function, 45 to 59 mild to moderate loss of kidney function, 60 to 89 indicates mild loss of kidney function, and 90 or higher indicates normal kidney function. The equation developed by the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) is used to estimate GFR from serum creatinine. The baseline value was selected as the value collected immediately prior to the initiation of immunosuppression withdrawal. The year 1, 2, and 3, values are the values closest to and within 2 months of the expected date. Change was calculated as the year 1, 2, or 3 value minus baseline. A positive value indicates an increase in kidney function.
Measured: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
Changes in Quality of Life in Tolerant Versus Non-tolerant Participants and in All Participants at Baseline Versus the End of Study Participation, as Measured by the NIDDK Liver Transplantation Database Quality of Life Form.
NIDDK Liver Transplantation Database Quality of Life Form is a patient-reported survey of patient health. The questionnaire is summarized into five domains-measures of disease (ranges from 0-21 with higher score indicating worse quality), psychological status (ranges from 0-5 with higher score indicating worse quality), personal function (ranges from 0-4 with higher score indicating better quality), social and role function (ranges from 0 to 20 with higher score indicating worse quality), and general health perception (ranges from 0 to 10 with higher score indicating better quality). Change was calculated as the difference between the questionnaire completed at the initiation of withdrawal and the questionnaire completed closest to the end of study participation. This change was calculated separately for tolerant and non-tolerant subjects.
Measured: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
Changes in SF-36 in Tolerant Versus Non-tolerant Participants and in All Participants at Baseline Versus the End of Study Participation.
SF-36 is a patient-reported survey of patient health. There are eight different scales that can be summarized into two summary scores-Mental Component Score and Physical Component Score. Each score ranges from 0-100, with a higher score indicating a better quality of life. Change was calculated as the difference between the questionnaire completed at the initiation of withdrawal and the questionnaire completed closest to the end of study participation. This change was calculated separately for tolerant and non-tolerant subjects.
Measured: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
Predictive Value of the Following Parameters With Regard to Operational Tolerance: Time Post-transplant.
Time post-transplant is calculated as time in years from transplant to enrollment. Participants are considered operationally tolerant if they remain off immunosuppression for at least 52 weeks without evidence of rejection since enrollment and have a liver biopsy at 52 weeks following completion of immunosuppression withdrawal demonstrating histological stability and the absence of rejection per Banff global assessment criteria (as assessed by the central pathologist). The odds ratio and corresponding 95% confidence interval are presented. The odds ratio represents the probability of achieving operational tolerance per year increase in time post-transplant. An odds ratio greater than 1 means that as the factor increases, operational tolerance is more likely to occur. Whereas less than 1 means operational tolerance is less likely to occur. Since the confidence interval contains 1, this means that as the corresponding factor increases, the likelihood of tolerance does not change.
Measured: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
Predictive Value and the Correlative Value of the Following Parameters With Regard to Operational Tolerance: Recipient Age.
Recipient age is the age at the time of enrollment. Participants are considered operationally tolerant if they remain off immunosuppression for at least 52 weeks without evidence of rejection since enrollment and have a liver biopsy at 52 weeks following completion of immunosuppression withdrawal demonstrating histological stability and the absence of rejection per Banff global assessment criteria (as assessed by the central pathologist). The odds ratio and corresponding 95% confidence interval are presented. The odds ratio represents the probability of achieving operational tolerance per year increase in recipient age. An odds ratio greater than 1 means that as the factor increases, operational tolerance is more likely to occur. Whereas less than 1 means operational tolerance is less likely to occur. Since the confidence interval contains 1, this means that as the corresponding factor increases, the likelihood of tolerance does not change.
Measured: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 Aug 2015 (estimated)
- Study start15 Dec 2015
- Primary completion10 Feb 2020
- Study completion8 Jul 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Liver TransplantStudies of the same condition, open and under way.
- More trials run by National Institute of Allergy and Infectious Diseases (NIAID)The sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 100 participants (actual)
Sponsor and investigators
- Sponsor type
- US National Institutes of Health
- Collaborators
- Immune Tolerance Network (ITN), PPD Development, LP, Rho Federal Systems Division, Inc.
- Responsible party
- Sponsor
- Investigators
- James F. Markmann, MD, PhD, Study chair, Massachusetts General Hospital: Transplantation
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02533180
- Sponsor's protocol ID
- DAIT ITN056ST
- Acronym
- OPTIMAL
- Status last verified
- Sep 2023
- First submitted
- 21 Aug 2015
- Last updated
- 14 Sep 2023
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
Publications
Sanchez-Fueyo A, Markmann JF. Immune Exhaustion and Transplantation. Am J Transplant. 2016 Jul;16(7):1953-7. doi: 10.1111/ajt.13702. Epub 2016 Feb 16.
PubMed 26729653
Study at a glance
From the registry record, last updated by the sponsor on 14 Sep 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Evaluation of Donor Specific Immune Senescence and Exhaustion as Biomarkers of Operational Tolerance Following Liver Transplantation in Adults (ITN056ST)
- ClinicalTrials.gov ID
- NCT02533180
- Acronym / sponsor ID
- OPTIMAL / DAIT ITN056ST
- Conditions
- Liver Transplant, Liver Transplantation
- Keywords
- Liver allograft recipient, Immunosuppression withdrawal, Calcineurin inhibitor (CNI) based immunosuppression, Living Donor (of the Respective Liver Transplant Recipient)
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 100 participants (actual)
- Lead sponsor
- National Institute of Allergy and Infectious Diseases (NIAID)US National Institutes of Health
- Collaborators
- Immune Tolerance Network (ITN), PPD Development, LP, Rho Federal Systems Division, Inc.
- Study start
- 15 Dec 2015 (actual)
- Primary completion
- 10 Feb 2020 (actual)
- Study completion
- 8 Jul 2022 (actual)
- First posted
- 26 Aug 2015 (estimated)
- Results
- Posted 5 Mar 2021
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The primary aim of this study is to determine whether a peripheral blood or graft lymphocyte phenotype of immune senescence or exhaustion is different between operationally tolerant and non-tolerant liver allograft recipients.
Detailed description
People who have liver transplants must take anti-rejection medication (immunosuppression) for the rest of their lives. If they stop, their immune system may reject the transplanted liver. All anti-rejection medications have side effects. Because of the side effects of anti-rejection medications, an important goal of transplant research is to allow people to accept their transplanted organ without long term use of anti-rejection medications. This is called tolerance. In this study, participants who received a liver transplant will have their anti-rejection medication(s) gradually reduced over a period of time and then stopped. The study calls this 'immunosuppression withdrawal'.
The purpose of this research study is to see how many people will develop tolerance after immunosuppression withdrawal. The researchers also want to find out if there are blood or liver biopsy tests that can help transplant doctors in the future predict whether it is safe to decrease or stop anti-rejection medications in people who received a liver transplant.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Immunosuppression withdrawal (ISW) | Other | Biological: Immunosuppression withdrawalGradual immunosuppression withdrawal according to the protocol defined algorithm |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (22 listed)
- Recipient participants must meet all of the following criteria to be eligible for this study:
- At the time of screening:
- Recipient of either deceased or living donor liver transplant. Recipients of living donor transplants must have a donor who is also willing to enroll
- Recipient of single organ transplant only
- Must have a screening liver biopsy that fulfills the following criteria based on the central pathology reading:
Key exclusion criteria (22 listed)
- Recipient participants who meet any of the following criteria will not be eligible for this study:
- History of hepatitis C virus (HCV) infection (defined as a positive HCV antibody test)
- Positive antigen-antibody immunoassay for human immunodeficiency virus, HIV-1/2
- Serum positivity for HBV surface antigen or HBV-DNA
- History of immune-mediated liver disease in which immunosuppression discontinuation is inadvisable (autoimmune hepatitis, primary sclerosing cholangitis, primary biliary cirrhosis)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Immunosuppression withdrawalAlso: ISWParticipants will initiate calcineurin inhibitor (CNI) withdrawal after at least 3 weeks of stable liver function, as documented by liver function tests (direct bilirubin, alanine aminotransferase and gamma-glutamyl transferase) separated by at least 1 week in the 3 week period prior to withdrawal. CNI withdrawal will occur in eight 3 week intervals with each subsequent reduction based on liver function tests over the prior 3 week interval. Participants on CNI and prednisone will undergo withdrawal from the two therapies concurrently. If participants are weaned off the CNI successfully, they will initiate non-CNI withdrawal. The non-CNI withdrawal includes two dose reductions of approximately 50% over a 6 week period each, after which the drug will be discontinued. | Biological | Immunosuppression withdrawal (ISW) |
Primary outcome
The Percent of Participants Who Achieve Operational Tolerance 52 Weeks After Completion of Immunosuppression Withdrawal.
Time frame: From initiation of immunosuppression withdrawal through 52 weeks after stopping all immunosuppression
Participants are considered as successfully withdrawn from immunosuppression if they remain off immunosuppression for at least 52 weeks without evidence of rejection since enrollment and have a liver biopsy at 52 weeks following completion of immunosuppression withdrawal demonstrating histological stability and the absence of rejection per Banff global assessment criteria. This biopsy is assessed by the central pathologist. All participants who fail to complete immunosuppression withdrawal, regardless of reason, or fail to have a biopsy 52 weeks after completion of immunosuppression withdrawal will be considered to have failed.
15 secondary outcomes
Proportion of Participants Who Develop Donor-Specific AlloAbs (DSA) or de Novo Anti-human Leukocyte Antigen Human Leukocyte Antigen (HLA) Antibodies
Time frame: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
The Incidence of Acute Rejection, Steroid Resistant Rejection, and Chronic Rejection
Time frame: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
The Severity of Acute Rejection, Steroid Resistant Rejection, and Chronic Rejection
Time frame: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
The Timing of Acute Rejection, Steroid Resistant Rejection, and Chronic Rejection
Time frame: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
The Incidence of Graft Fibrosis in Tolerant Versus Non- Tolerant Patients.
Time frame: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
The Progression of Graft Fibrosis in Tolerant Versus Non- Tolerant Patients
Time frame: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
The Incidence of Graft Loss
Time frame: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
The Incidence of All-Cause Mortality
Time frame: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
The Incidence of Study-related SAEs
Time frame: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
The Proportion of Operationally Tolerant Subjects Who Remain Free of Rejection at 3 Years After Completing Immunosuppression Withdrawal.
Time frame: From initiation of immunosuppression withdrawal through 3 years after completing immunosuppression withdrawal.
Changes in Renal Function (Defined as Estimated GFR Calculated by the CKD-EPI Creatine Equation 2021) in Tolerant Versus Non-tolerant Participants at 1, 2 and 3 Years After Completing Immunosuppression Withdrawal.
Time frame: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
Changes in Quality of Life in Tolerant Versus Non-tolerant Participants and in All Participants at Baseline Versus the End of Study Participation, as Measured by the NIDDK Liver Transplantation Database Quality of Life Form.
Time frame: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
Changes in SF-36 in Tolerant Versus Non-tolerant Participants and in All Participants at Baseline Versus the End of Study Participation.
Time frame: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
Predictive Value of the Following Parameters With Regard to Operational Tolerance: Time Post-transplant.
Time frame: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
Predictive Value and the Correlative Value of the Following Parameters With Regard to Operational Tolerance: Recipient Age.
Time frame: From initiation of immunosuppression withdrawal to study completion, up to 4.5 years.
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 14 Sep 2023.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Derived from this study: PubMed 26729653Sanchez-Fueyo A, Markmann JF. Immune Exhaustion and Transplantation. Am J Transplant. 2016 Jul;16(7):1953-7. doi: 10.1111/ajt.13702. Epub 2016 Feb 16.
- ITN OPTIMAL Study WebsiteLink provided by the sponsor.
- Division of Allergy, Immunology, and Transplantation (DAIT)Link provided by the sponsor.
- National Institute of Allergy and Infectious Diseases (NIAID)Link provided by the sponsor.
- Immune Tolerance Network (ITN)Link provided by the sponsor.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
James F. Markmann, MD, PhD study chair
Massachusetts General Hospital: Transplantation
7 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing Immunosuppression withdrawal in people with Liver Transplant and Liver Transplantation, run by National Institute of Allergy and Infectious Diseases (NIAID) at 7 sites in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 22 inclusion and 22 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 14 Sep 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 7 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Yes. Results are posted in the registry (first posted 5 Mar 2021). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
The Percent of Participants Who Achieve Operational Tolerance 52 Weeks After Completion of Immunosuppression Withdrawal. (time frame: From initiation of immunosuppression withdrawal through 52 weeks after stopping all immunosuppression). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT02533180, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Sep 2023.