BENITIONSClinical Trial Intelligence

Precision Guided Tacrolimus Dosing in Pediatric Heart Transplant

不适用 已完成 NCT04380311

适应症Heart Transplant Failure and Rejection
分期不适用
申办方University of Utah
状态已完成
受试者人数17 人
干预(药物)Tacrolimus Dosing Support Tool
开始日期2020年5月1日
完成日期2025年4月30日
结果公布日2026年8月3日

摘要

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

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本页整理自 ClinicalTrials.gov 的公开数据,不构成医疗建议,也不构成投资建议。请务必咨询专业医师。