BENITIONSClinical Trial Intelligence

Precision Guided Tacrolimus Dosing in Pediatric Heart Transplant

N/A Completed NCT04380311

ConditionHeart Transplant Failure and Rejection
PhaseN/A
SponsorUniversity of Utah
StatusCompleted
Enrollment17 participants
InterventionsTacrolimus Dosing Support Tool
Start dateMay 1, 2020
Completion dateApr 30, 2025
Results postedAug 3, 2026

Summary

Immunosuppressive therapy is required to prevent organ rejection, however, dosing of immunosuppressive agents is complicated by patient-specific differences impacting the body's absorption and elimination of these agents. The goal of this research proposal is to clinically validate an innovative precision medicine strategy for dosing the immunosuppressant tacrolimus in pediatric heart transplant, which will in turn lead to improvements in long-term transplant survival outcomes. The strategy and techniques used in this project can be extended to improve drug therapy across multiple pediatric diseases requiring chronic therapy.

Time to Target Concentration Attainment

Within 6 weeks following transplant · days

Personalized Tacrolimus Dosing6.93 ± 3.59 days
p-value0.03

Open in BENITIONS View on ClinicalTrials.gov

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