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Study to Compare the Outcome of Receiving Continued Immunosuppression Versus Stopping Immunosuppression at 6 Months to Safely Prevent Human Leukocyte Antigen (HLA) Sensitization in Patients With Late Renal Graft Failure

Phase 4
Recruiting
Conditions
Renal Failure , Chronic
Graft Failure
Graft Rejection
Allograft
Renal Failure Chronic Requiring Dialysis
Interventions
Drug: Calcineurin inhibitor withdrawal at 6 months
Drug: Continue low dose calcineurin inhibitor (CNI)
Registration Number
NCT06676696
Lead Sponsor
Hospital Universitari Vall d'Hebron Research Institute
Brief Summary

The goal of this clinical trial is to compare the degree of HLA sensitization at 2 years in patients with late renal graft failure (\> 3 months) when receiving reduced immunosuppressant treatment versus stopping immunosuppression at 6 months.

The main question this study aims to answer is:

Does maintaining long-term immunosuppression in patients with a late renal graft failure (\> 3 months) safely reduce the risk of HLA sensitization?

To answer this question, patients will be assigned to a control arm or investigational arm:

* Patients assigned to the control arm will receive standard treatment, in which immunosuppressant treatment is withdrawn after 6 months.

* Patients assigned to the investigatonal arm will continue immunosuppressant treatment at low doses for 2 years.

Patients recruited in this clinical trial will be followed for up to 2 years. During this time, patients will visit the clinic every 3 months for checkups and tests.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
202
Inclusion Criteria
  • Patient must be able to understand and provide written informed consent
  • Patients older than 18 years who had received at least one previous renal transplant
  • Patients with a retained kidney graft failed for any reason which survived at least 3 months
  • Patients on dialysis, either hemodialysis or peritoneal dialysis. Patients can be on dialysis for a maximum of 6 months at the time of randomization, as long as the patients have taken an uninterrupted immunosuppressive regimen of calcineurin inhibitors (tacrolimus or cyclosporine) and steroids since dialysis was restarted
  • Patients already relisted or candidates to relist to deceased donor kidney transplantation according to the treating physician criteria
  • Patients taking immunosuppressants tacrolimus or cyclosporine
  • cPRA at the time of randomization ≤ 90%
Exclusion Criteria
  • Patients who have received another solid organ transplantation (liver, lung, heart or pancreas)
  • Patients waiting for a living related / unrelated kidney transplant
  • Graft survival of the failed graft lower than 3 months
  • Patients in dialysis more than 6 months at the time of randomization
  • Patients not accomplishing criteria to relist in the transplantation list according to the treating physician criteria
  • Pregnant women
  • Females of childbearing age who have not used or do not plan to use acceptable birth control measures, for the duration of the study. Patients should use one of the acceptable birth control measures recommended in the document "Recommendations related to contraception and pregnancy testing in clinical trials" published by the Clinical Trials Facilitation and Coordination Group (CTFG) (version 1.1, published 21/09/2020). Recommended birth control measures include oral, injected or implanted hormonal contraceptive, barrier methods (condom or diaphragm with spermicide), intrauterine device, surgical sterilization, transdermal delivery, or sexual abstinence. If sexually active, the subject must have been using one of the accepted birth control methods at least one month prior to study entry.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Control ArmCalcineurin inhibitor withdrawal at 6 months-
Investigational armContinue low dose calcineurin inhibitor (CNI)-
Primary Outcome Measures
NameTimeMethod
Degree of HLA sensitization2 years

The difference between the two treatment arms in the degree of HLA sensitization at 2-years measured as cPRA (%).

Secondary Outcome Measures
NameTimeMethod
Incidence of infection2 years

The difference between the two treatment arms at 2-years on incidence of infection

Incidence of cardiovascular events2 years

The difference between the two treatment arms at 2-years on incidence of cardiovascular events

Incidence of cancer2 years

The difference between the two treatment arms at 2-years on incidence of cancer

Incidence of graft-intolerance syndrome requiring graft nephrectomy or percutaneous embolization of the non-functioning graft2 years

The difference between the two treatment arms at 2-years incidence of graft-intolerance syndrome requiring graft nephrectomy or percutaneous embolization of the non-functioning graft

Erythropoietin resistance index2 years

The difference between the two treatment arms at 2-years on erythropoietin resistance index

Residual renal function2 years

The difference between the two treatment arms at 2-years on residual renal function

Number of circulating memory B-cells2 years

The difference between the two treatment arms at 2-years on number of circulating memory B-cells

Adverse events2 years

The difference in the incidence of adverse events (AE) in the two treatment arms

Percentage of patients delisted for any reason2 years

The difference between the two treatment arms at 2-years on percentage of patients delisted for any reason

Mortality for any reason2 years

The difference between the two treatment arms at 2-years on mortality for any reason

Days of hospitalization for any reason2 years

The difference between the two treatment arms at 2-years on days of hospitalization for any reason

Percentage of patients effectively relisted during follow-up2 years

The difference between the two treatment arms at 2-years on percentage of patients effectively relisted during follow-up

Percentage of patients transplanted2 years

The difference between the two treatment arms at 2-years on percentage of patients transplanted

Trial Locations

Locations (1)

Hospital Universitario Vall D'Hebron

🇪🇸

Barcelona, Spain

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