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临床试验/NCT04063865
NCT04063865终止3 期

Protection of Renal Function After Liver Transplant Using Everolimus Monotherapy as the Immunosuppression Regimen

Indiana University1 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2019年5月9日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
终止
入组人数
14
试验地点
1
主要终点
Long-Term Renal Function With Tacrolimus Monotherapy

研究概览

简要总结

Tacrolimus is the standard immunosuppressive drug used to prevent organ rejection post liver transplant. One side effect of Tacrolimus is nephrotoxicity. Everolimus does not have the nephrotoxicity side effects of Tacrolimus.

Replacement of Tacrolimus by Everolimus may have a reduced incidence of renal dysfunction in liver transplant patients who have near normal kidney function prior to liver transplantation. Other investigators have already shown a benefit in terms of renal function with introduction of Everolimus with reduced-exposure tacrolimus at 1 month after liver transplantation, this benefit has been shown was maintained to 3 years in patients who continued Everolimus therapy with comparable efficacy and no late safety concerns. Investigators in this trial are proposing to advance this approach further by completely eliminating Tacrolimus from patients' immunosuppression protocol. The rationale for this approach is based on a unique induction immunosuppression protocol.

Liver transplant patients receive potent induction immunosuppression in the form of rabbit anti thymocyte globulin.

Investigators believe that in conjunction with this induction regimen, patients can be maintained on Everolimus monotherapy without the risk of rejection. By completely eliminating Tacrolimus, investigators believe that there may be further benefit in terms of renal function. Additionally, Everolimus is known to induce tolerance in transplant recipients. Tolerant patients do not require immunosuppression to accept transplant organs.

The long-term efficacy and safety of Everolimus monotherapy as the maintenance immunosuppression in patients receiving rATG induction is unknown.

Primary Aim: Assess the effect of Everolimus monotherapy versus Tacrolimus monotherapy on long term renal function measured by Glomerular Filtration Rate (GFR).

详细描述

Following enrollment, subjects will be randomized at one month post transplant to Tacrolimus (control) or to Everolimus (study) as maintenance immunosuppression.

After liver transplant, all patients will receive the standard induction regimen and Tacrolimus monotherapy.

INDUCTION:

Rabbit anti-thymocyte globulin (rATG) 1.5 mg/kg of actual body weight rounded to nearest 25 mg and capped at 150 mg for up to three doses given IV on post-operative day (POD) 1, 3, and 5. Some patients may receive only one dose if considered too frail to need all three doses.

30 minutes prior to infusion, pre-medicate with the following: Daily steroid dose Acetaminophen (Tylenol®) 650 mg PO or per nasogastric (NG) x 1 dose Diphenhydramine (Benadryl®) 25 mg IV push x 1 dose

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Liver transplant recipients >= 18 years old
  • Normal baseline renal dysfunction (GFR > 60 mL/min)
  • Rabbit anti-thymocyte globulin (rATG) induction (cumulative dose 1.5 - 5 mg/kg)
  • Indication for transplant: ethanol, hepatitis C, or nonalcoholic steatohepatitis or any combination of these

排除标准

  • Increased risk of rejection: autoimmune hepatitis, primary biliary cirrhosis, primary sclerosing cholangitis, positive crossmatch, retransplantation
  • Incompletely healed incision or other wound healing issues at time of randomization
  • Multiple or previous organ transplantation
  • Severe, uncontrolled hypercholesterolemia (> 9mmol/L) or hypertriglyceridemia (>8.5 mmol/L) in the 6 months prior to transplantation
  • Insurance company unwilling to pay for the cost of the everolimus or patient does not qualify for the Novartis Patient Assistance Program.
  • Pregnant women
  • Unable to provide informed consent

研究组 & 干预措施

Control Arm

Active Comparator

Tacrolimus as maintenance immunosuppression

干预措施: Tacrolimus (Drug)

Study Arm

Experimental

Everolimus monotherapy maintenance immunosuppression

干预措施: Everolimus (Drug)

结局指标

主要结局

Long-Term Renal Function With Tacrolimus Monotherapy

时间窗: 36 months post-transplant

Glomerular Filtration Rate

Long-Term Renal Function With Everolimus Monotherapy

时间窗: 36 months post-transplant

Glomerular Filtration Rate

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Chandrashekhar Kubal

Princial Investigator

Indiana University

研究点 (1)

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