Safety of Immunosuppression Minimization in Children and Adolescents After Kidney Transplantation

National Institute of Allergy and Infectious Diseases (NIAID)

Status and phase: Completed; Phase 1

Conditions: Kidney Transplantation; Immunosuppression; Kidney Failure, Chronic

Treatments: Drug: Sirolimus; Drug: MMF or Azathioprine

Study type: Interventional

Funder types: NIH

Identifiers

NCT00768729

DAIT CTOTC-01

Details and patient eligibility

About

Kidney transplantation is widely considered to be the treatment of choice for children with End Stage Renal Disease (ESRD). The purpose of this study is to determine the safety of sirolimus monotherapy for long-term immunosuppression in children and adolescents after kidney transplantation.

Full description

Improvements in surgical techniques, donor selection, immunosuppression practices, and the enhanced experience of specialized pediatric transplant teams have all led to marked improvements in patient and kidney graft survival in infants and young children Long-term graft survival rates decrease in adolescents 11 to 17 years of age. Several studies have suggested this decrease may be the result of noncompliance with immunosuppressive medications in this age group. Therefore, protocols that minimize the use of immunosuppressive medications, while retaining kidney function are necessary for improving graft and patient survival in children. The purpose of this study is to determine the safety of sirolimus monotherapy for long-term immunosuppression in children and adolescents after kidney transplantation.

This study will enroll 10 participants who previously completed the CCTPT-PC01 study. The accrual period is scheduled for 12 months. The study follow-up period will last 96 weeks. Patients from the CCTPT-PC01 study have been maintained on sirolimus and mycophenolate mofetil (MMF) since 2-3 months post transplant. Enrolled participants receiving (MMF) or Azathioprine at study entry will have their doses withdrawn gradually over a period of 6 months. Dosage will be reduced by 25% initially and by 25% every 2 months resulting in complete withdrawal by 6 months.

This study will consist of 11 study visits after screening and study entry. Study visits will occur at weeks 1, 8, 16, 24, 32, 40, 48, 60, 72, 84, and 96. A physical exam, vital signs, sirolimus levels, as well as blood and urine collection will occur at all visits. A renal biopsy will be performed at week 96.

Enrollment: 7 patients

Sex: All

Ages: 1 to 20 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Participant and/or parent guardian able to understand and willing to provide informed consent
• Previously enrolled and completed the CCTPT-PC01 study and within the 36 months post-completion timeframe prior to study entry
• Currently receiving sirolimus and MMF or azathioprine therapy
• No history of acute rejection episodes
• No evidence of acute or chronic rejection on the 24 month CCTPT-PC01 protocol biopsy or any subsequent biopsy obtained after that time prior to study entry
• PRA (Class I and II) less than 5% at study entry
• No evidence of donor specific antibody at study entry
• Stable renal function with GFR greater than 60 cc/min 1.73M^2 using the Schwartz calculated method
• A negative pregnancy test for female participants of childbearing potential at study entry
• Agreement by female and male participants to use FDA approved methods of contraception.

Exclusion criteria

• Total lymphocyte count less than 400 mm^3
• Acute or chronic infection at study entry
• Treatment with investigational drug within 1 month prior to study entry
• Mental illness or history of drug or alcohol abuse that, in the opinion of the investigator, would interfere with the study
• History of allergic reaction to Iodine GFR assay
• History of malignancy within the past 12 months
• Inability or unwillingness to give informed consent or comply with the study protocol

Trial design

Primary purpose: Prevention

Allocation: Non-Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)

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7 participants in 1 patient group

1

Experimental group

Description:

Participants who have been maintained on MMF at study entry will start the study on 600 mg/m2 MMF orally daily. Participants who have been maintained on Azathioprine due to MMF intolerance will receive 1 mg/kg Azathioprine orally daily. Participants will continue receiving sirolimus throughout the study. However, MMF or Azathioprine will be withdrawn gradually over a period of at least 6 months. Dosage will be reduced by 25% initially and by 25% every subsequent 2 months resulting in complete withdrawal by 6 months.

Treatment:

Drug: MMF or Azathioprine

Drug: Sirolimus