Phase 4
N=52
Kidney Biopsy Controlled Trial of Calcineurin Inhibitor Withdrawal
Kidney Transplantation
Bottom Line
View on ClinicalTrials.gov: NCT00896012 ↗Enrolled (actual)
52
Serious AEs
19.2%
Results posted
Dec 2020
Primary outcome: Primary: Number of Participants With Graft Survival at 12 Months — 18; 12 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 4
- Interventions
- Kidney Biopsy (Procedure); Rapamune (sirolimus/rapamycin) (Drug); Tacrolimus (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- University at Buffalo
- Primary completion
- Nov 2011
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Participants With Graft Survival at 12 Months |
18; 12 | — |
| PRIMARY Either Equivalent or Improved Estimated Glomerular Filtration Rate (eGFR) at One Year in the Rapamycin Group |
65.5; 58.3; 68.6; 58.7; 75; 67 | 0.222 |
| PRIMARY Improved Histology at 12 Months in the Rapamycin Group |
1.1; 1.0; 2.8; 2.0 | — |
Summary
Current therapy to prevent organ rejection relies on the use of calcineurin inhibitors either cyclosporine or tacrolimus. Although these agents have been very successful in preventing early acute rejection, this success has not translated into improved long-term kidney transplant function. One of the important factors that leads to premature kidney transplant failure is chronic allograft nephropathy (CAN). CAN is characterized by progressive interstitial fibrosis or "scarring", vascular wall thickening, and finally glomerular sclerosis leading to slow progressive loss of kidney function. Calcineurin inhibitors have been shown to play an important role in the pathogens of CAN. Renal transplant recipients in whom calcineurin inhibitors are discontinued enjoy better and longer kidney function. Therefore, immunosuppressive strategies are being designed with the intention of withdrawing calcineurin inhibitors.
The purpose of this trial is to test if tacrolimus can be safely substituted by sirolimus (Rapamycin) and this substitution will yield improved renal function, less CAN and better graft survival rates over the first year.
Eligibility Criteria
Inclusion Criteria
- All patients receiving their first renal allograft transplant will be considered eligible for study
- Patients receiving both living and cadaveric donors will be eligible
Exclusion Criteria
- If less than 18 years of age
- Severe hyperlipidemia
- If pregnant or cannot comply with proper birth control during the study
- Recipients of kidney together with another solid organ or bone marrow transplant
- Patients receiving any investigational medications or participating in a clinical trial
- Patients receiving a second or third renal allograft
- PRA > 30%
- Active infections
- Chronic antiarrhythmic therapy for ventricular arrhythmia
- Malignancy except for basal cell carcinoma
- HIV
- ANC count 400 mg/dl and cholesterol > 300 mg/dl
- HCV-positive, HBVSAg-positive, HBVCoreAb-positive and HBVSAntibody negative or HCV/HBV co-infected patients
- Breastfeeding women
Data sourced from ClinicalTrials.gov (NCT00896012). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.