Bela 8 Week Dosing

Emory University166 enrolled

Overview

The purpose of this study is to transition patients who have been stable on Belatacept for one year after kidney transplant from standard 4-week to an investigational 8-week belatacept dosing schedule. The investigators hypothesize that renal function and acute rejection rates will be non-inferior with 8-week belatacept dosing.

The current dosing protocol for patients who have undergone a kidney transplant requires that Belatacept be given as an infusion every 4 weeks. The investigator wants to assess if the patients who have been stable for one year after transplant can be safely transitioned to an 8-week Belatacept infusion schedule. Renal function and any episodes of acute rejection will be closely monitored.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

SUPPORTIVE_CARE

Masking

NONE

Enrollment

166

Conditions

Kidney Transplantation

Interventions

BelataceptDRUG

Belatacept is an immunosuppressive medication and will be given as an intravenous infusion at a dose of 5 mg/kg at 4-weekly or 8-weekly intervals.

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Adult (age ≥18 years currently), * First-time renal transplant recipients of either living donor or deceased donor, 1. who were initiated on belatacept at the time of transplant and 2. are at least one year post-transplant and off CNI therapy for at least 6 months. * Patients at low immunologic risk, defined as 1. patients with a first transplant who have a PRA \< 50 against class I and class II antigens, 2. no DSA (donor-specific antibodies), 3. who have not had more than one episode of rejection, and 4. no episodes of rejection within the last 6 months prior to enrollment, and 5. no rejection with a grade of IIB or above. Exclusion Criteria: * Not first renal transplant, or multi-organ transplant recipient * History of greater than one episode of biopsy-proven acute rejection, or of rejection of Banff 97 grade IIB or greater, or rejection within the last 6 months. * Pregnancy (women of childbearing potential must use adequate contraception during study) * Unwilling to receive all belatacept infusions at the Emory Transplant Center * Calculated Glomerular Filtration Rate (GFR) less than 35. * Serum creatinine at enrollment over 30% higher than 3 months (±4 weeks) prior to randomization * HbA1C greater than 8 at enrollment * Recent history of significant proteinuria (protein/Cr ratio \>1) * Non-standard belatacept dosing (e.g. dose other than 5 mg belatacept/kg body weight) * Cellcept dose less than 500 mg po bid. * Prednisone dose greater than 5mg po qd within 3 months of randomization * Patients not currently taking prednisone * Active infection, or antibiotic or antiviral drug therapy within 1 month of randomization * Evidence of Cytomegalovirus (CMV) viremia or clinical CMV infection within last 3 months. * Polyomavirus BK PCR (polymerase chain reaction) load greater then 4.3 (copy number greater than 20,0000) within 3 months of randomization * Known hepatitis B surface antigen-positive or PCR-positive for hepatitis B (testing not required) * Known HIV (human immunodeficiency virus infection) (testing not required) * Presence of donor specific antibody by Luminex single antigen assessment, or panel reactivity (PRA) above 50%. * History of substance abuse or psychiatric disorder not compatible with study adherence and follow up.

Locations (2)

Emory Clinic

Atlanta, Georgia, United States

Emory University Hospital

Atlanta, Georgia, United States

Outcomes

Primary Outcomes

Mean Estimated Glomerular Filtration Rate (eGFR) at 12 Months From Baseline

The mean estimated Glomerular Filtration Rate (eGFR) will be calculated according to the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation using serum creatinine measurements and the patient's age, gender, and race. An eGFR below 60 ml/min/1.73 m\^2 indicates lower renal function.

Time frame: 12 months from baseline

Secondary Outcomes

Number of Participants With Transplant Rejection at 6 Months and 12 Months Post Baseline

The number of occurrences of transplant rejection at 6 months and 12 months from baseline will be recorded.

Time frame: 6 months post baseline, 12 months post baseline

Number of Subjects With Grade IIA and Lower Rejections at 6 Months and 12 Months Post Baseline

The number of subjects with Grade IIA and lower severity of rejection on the Banff 97 diagnostic categories will be recorded. The severity of acute rejections will be graded based on histopathological findings; Grade IA= significant interstitial infiltration and moderate tubulitis; Grade IB= significant interstitial infiltration and severe tubulitis; Grade IIA= mild to moderate intimal arteritis; Grade IIB= severe intimal arteritis and Grade III= transmural arteritis and/or fibrinoid change and necrosis of cells.

Time frame: 6 months post baseline, 12 months post baseline

Number of Subjects With Grade IIB and Higher Rejections at 6 Months and 12 Months Post Baseline

The number of subjects with Grade IIB and higher severity of rejection on the Banff 97 diagnostic categories will be recorded. The severity of acute rejections will be graded based on histopathological findings; Grade IA= significant interstitial infiltration and moderate tubulitis; Grade IB= significant interstitial infiltration and severe tubulitis; Grade IIA= mild to moderate intimal arteritis; Grade IIB= severe intimal arteritis and Grade III= transmural arteritis and/or fibrinoid change and necrosis of cells.

Data from ClinicalTrials.gov

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