drugset / Trial / NCT03386539

Tacrolimus/Everolimus vs. Tacrolimus/MMF in Pediatric Heart Transplant Recipients Using the MATE Score

NCT03386539

RandomizedParallel-groupSingle-blindTreatment

Summary

The TEAMMATE Trial will enroll 210 pediatric heart transplant patients from 25 centers at 6 months post-transplant and follow each patient for 2.5 years. Half of the participants will receive everolimus and low-dose tacrolimus and the other half will receive tacrolimus and mycophenolate mofetil. The trial will determine which treatment is better at reducing the cumulative risk of coronary artery vasculopathy, chronic kidney disease and biopsy proven-acute cellular rejection without an increase in graft loss due to all causes (e.g. infection, PTLD, antibody mediated rejection).

Timeline

Start
2018-01-29
Primary completion
2023-04-17
Completion
2024-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Everolimus Small molecule 0.6 mg/m2 Oral
Comparator Mycophenolate Mofetil Small molecule 600 mg/m2 Oral
Subject Tacrolimus Small molecule 0.0125 mg/kg Oral
Subject Tacrolimus Small molecule 0.05 mg/kg Oral