Precision Guided Tacrolimus Dosing in Pediatric Heart Transplant
不适用
已完成
NCT04380311
| 适应症 | Heart Transplant Failure and Rejection |
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| 分期 | 不适用 |
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| 申办方 | University of Utah |
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| 状态 | 已完成 |
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| 受试者人数 | 17 人 |
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| 干预(药物) | Tacrolimus Dosing Support Tool |
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| 开始日期 | 2020年5月1日 |
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| 完成日期 | 2025年4月30日 |
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| 结果公布日 | 2026年8月3日 |
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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 Dosing | 6.93 ± 3.59 days |
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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。