A Study to Compare Treatment With Sirolimus Versus Standard Treatment in Patients Who Have Received a Kidney Transplant

NCT ID: NCT00005113

Last Updated: 2012-03-13

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE3
• Total Enrollment: 102 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 1999-07-31
• Study Completion Date: 2006-03-31

Brief Summary

The purpose of this study is to compare treatment with the new drug sirolimus (SRL) versus the standard treatment with cyclosporine (CsA) or tacrolimus in children who have received kidney transplants. SRL is a new medication that may prevent the body's immune system from rejecting organ transplants.

After receiving a kidney transplant, the body recognizes the donated kidney as a foreign invader and triggers the immune system to attack the kidney. This can lead to rejection of the new kidney and a failed transplant. To help reduce the risk of kidney rejection, transplant patients are given immunosuppressant drugs, which reduce the body's normal immune response and allow the transplanted organ to function. CsA or tacrolimus are two drugs that are often given to transplant patients. However, these are powerful drugs, and it can cause serious side effects and put a patient at increased risk for infections. SRL is a new drug that has been shown to reduce a transplant patient's chance of rejecting a new kidney, without serious side effects. This study is necessary to test the safety and effectiveness of SRL in children.

Detailed Description

Successful kidney transplantation has gradually improved over the years; much of the improvement has resulted from the use of CsA. However, adequate and tolerable immunosuppression is difficult to achieve with CsA, and rejection episodes are still frequent. CsA is nephrotoxic, with drug toxicity often masking rejection episodes. Other immunosuppressant therapies can result in a range of complications, including metabolic disturbances, adrenocortical insufficiency, and increased risk for infections. Therefore, more effective drugs with less toxicity are needed to prevent acute rejection, especially in the pediatric population where the overall graft survival rate remains significantly lower when compared with that of adult transplant recipients. SRL is an immunosuppressive agent being developed for the prophylaxis of acute renal allograft rejection. SRL has a unique mechanism of action. It inhibits T and B cell activity. In Phase I and II trials in adults, SRL was generally well tolerated and exhibited no apparent nephrotoxic properties, and significantly lower rates of rejection were seen with SRL when compared to placebo.

Patients receive extensive prestudy screening, which includes a renal core biopsy, chest x-ray, bone density study, blood tests, and glomerular filtration rate (GFR). Patients are then randomly assigned to 1 of 2 study treatment groups in a 2:1 ratio (142 patients receive SRL, CsA/tacrolimus, and corticosteroids and 71 patients receive standard CsA or tacrolimus-based double or triple drug therapy). SRL is administered as an oral dose of 3 mg/m2/day. Patients are followed for 3 years on therapy, and then for 1 month of follow-up. A renal core biopsy is performed at the time of study entry and at Months 6, 18, and at early termination of patient in study. Patients undergo physical examinations and various blood tests at specified time intervals during the 37-month study period. Efficacy is assessed by comparing the composite endpoint of biopsy-proven acute rejection, graft loss, or death after 36 months of treatment. Safety is assessed by comparing the composite endpoint of graft loss or death after 36 months of treatment.

Conditions

End-Stage Renal Disease; Kidney Transplantation

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

1

Participants will receive SRL, CsA/tacrolimus, and corticosteroids for up to 36 months

Group Type: EXPERIMENTAL

Cyclosporine

Intervention Type: DRUG

Oral tablet taken daily. Dosage is dependent on weight and is titrated to target trough level.

Sirolimus

Intervention Type: DRUG

Dosage in liquid or tablet form is dependent on body surface area and is titrated to target trough level.

Tacrolimus

Intervention Type: DRUG

dosage is in oral form titrated to target trough level

2

Participants will receive standard CsA or tacrolimus-based double or triple drug therapy for up to 36 months

Group Type: EXPERIMENTAL

Cyclosporine

Intervention Type: DRUG

Oral tablet taken daily. Dosage is dependent on weight and is titrated to target trough level.

Tacrolimus

Intervention Type: DRUG

dosage is in oral form titrated to target trough level

Interventions

Cyclosporine

Oral tablet taken daily. Dosage is dependent on weight and is titrated to target trough level.

Intervention Type: DRUG

Sirolimus

Dosage in liquid or tablet form is dependent on body surface area and is titrated to target trough level.

Intervention Type: DRUG

Tacrolimus

dosage is in oral form titrated to target trough level

Intervention Type: DRUG

Other Intervention Names

CsA; SRL

Eligibility Criteria

Inclusion Criteria

Your child may be eligible for this study if he/she:

• Has received a kidney transplant.
• Has experienced 1 or more episodes of acute rejection or chronic rejection; a rejection episode must have responded to treatment and have occurred at least 30 days before study enrollment.
• Has stable kidney function at the time of study enrollment.
• Is 20 years of age or younger.
• Has written informed consent of parent or guardian if under the age of 18.
• Agrees to use birth control during the study and for 3 months following treatment.

Exclusion Criteria

Your child will not be eligible for this study if he/she:

• Has a history of cancer.
• Has received a multi-organ transplant (more than a kidney).
• Has an active infection.
• Has an abnormal chest X-ray.
• Cannot provide a kidney biopsy at time of study entry.
• Is allergic to sirolimus.
• Has received experimental drugs within 4 weeks of study entry.
• Is pregnant.

• Maximum Eligible Age: 20 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Boston Children's Hospital

OTHER

Sponsor Role: lead

Responsible Party

William Harmon

Director, Division of Nephrology

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Children's Hospital Boston

Boston, Massachusetts, United States

Countries

United States

Other Identifiers

DAIT 0468E1-217-US

Identifier Type: -

Identifier Source: secondary_id

DAIT SRL1

Identifier Type: -

Identifier Source: org_study_id