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临床试验/NCT04773392
NCT04773392终止4 期

SIMPLE Study: A Prospective and Randomized Trial of a Simplified Immunosuppressive Protocol Utilizing Low Dose EnvarsusXR

University of Southern California1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2021年11月23日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
终止
入组人数
20
试验地点
1
主要终点
To compare the composite incidence of biopsy proven acute rejection, graft survival and patient survival

研究概览

简要总结

The purpose of this study is to determine if the combination of once-daily tacrolimus extended-release (EnvarsusXR) and Azathioprine is non inferior with respect to the composite outcome of acute rejection, graft and patient survival as compared to a combination of twice-daily immediate release tacrolimus and mycophenolate mofetil/mycophenolic acid.

详细描述

While short-term graft outcomes in kidney transplantation have improved, this requires adherence to a complex medication regimen. The current twice-daily immunosuppressive regimen, immediate release tacrolimus and mycophenolate mofetil/mycophenolic acid, has reduced rejection rates significantly, but frequently cause neurologic and gastrointestinal side effects which impact recipient quality of life. These side effects often require dose adjustments and studies have shown inferior outcomes when multiple changes are made to the immunosuppressive regimen. Furthermore, patients taking twice-daily medications have poorer compliance and yet adherence to these medications is critical to mitigate the risk of allograft rejection. Acute and chronic rejection are important causes of graft failure and patient survival.

Immediate release (IR) tacrolimus based immunosuppressive regimens have become the standard of care at most US centers. With the introduction of a once-daily tacrolimus formulation, kidney transplant recipients can now be on a combination regimen (EnvarsusXR and azathioprine) that permits all immunosuppressive medications to be taken once a day instead of twice . Previous studies suggest that therapeutic goals with EnvarsusXR may be achieved at a lower dose than the currently recommended dose. This once a day medication schedule has the potential to simplify the immunosuppressive regimen by reducing adverse side effects and facilitating compliance.

The investigators seek to demonstrate that a once-daily regimen, including EnvarsusXR and azathioprine, will be at least equally effective with respect to acute rejection, graft and patient survival as compared to the standard, twice-daily, immediate release tacrolimus and mycophenolate mofetil/mycophenolic acid. The investigators will also assess graft function, medication complications and side effects in each arm.

研究设计

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

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •De- Novo Kidney transplant patients between 18 and 85 years old
  • •Cold ischemia time (CIT) < 24 hours for 3-6 HLA mismatches between donor and recipient and CIT >24 hours for HLA mismatch of less than 3 between donor and recipient
  • •Most recent pre-transplant cPRA (calculated panel reactive antibody) ≤ 20%

排除标准

  • •Repeat kidney transplant recipients
  • •cPRA >20%
  • •rATG (rabbit anti-thymocyte globulin) induction >6mg/kg at time of induction
  • •Crossmatches deemed positive by accepting physician
  • •Presence of pre-formed anti-HLA (anti-Human Leukocyte Antigen) DSA (Donor-Specific Antibody) as defined by MFI (mean fluorescence intensity) approaching 3000 using flow cytometry/Luminex-based, specific anti-HLA antibody testing.
  • •Receipt of desensitization protocols
  • •History of skin cancer
  • •Recipient of multi-organ or dual kidney transplants
  • •For any condition, in which the investigator's opinion makes the subject unsuitable for study

研究组 & 干预措施

Twice-daily Regimen

Active Comparator

Twice-daily regimen of immediate release tacrolimus, mycophenolate mofetil (MMF)/mycophenolic acid (MPA) plus daily methylprednisolone or prednisone.

干预措施: Mycophenolate mofetil (MMF) or Mycophenolic acid (MPA) (Drug)

Once-daily Regimen

Active Comparator

Once-daily regimen of Envarsus, azathioprine plus methylprednisolone or prednisone.

干预措施: Once-daily envarsus XR (Drug)

Once-daily Regimen

Active Comparator

Once-daily regimen of Envarsus, azathioprine plus methylprednisolone or prednisone.

干预措施: Azathioprine (Drug)

Once-daily Regimen

Active Comparator

Once-daily regimen of Envarsus, azathioprine plus methylprednisolone or prednisone.

干预措施: Methylprednisolone, prednisone (Drug)

Once-daily Regimen

Active Comparator

Once-daily regimen of Envarsus, azathioprine plus methylprednisolone or prednisone.

干预措施: Induction Immunosuppression with Basiliximab or Rabbit Anti Thymoglobulin (rATG) (Drug)

Twice-daily Regimen

Active Comparator

Twice-daily regimen of immediate release tacrolimus, mycophenolate mofetil (MMF)/mycophenolic acid (MPA) plus daily methylprednisolone or prednisone.

干预措施: Methylprednisolone, prednisone (Drug)

Twice-daily Regimen

Active Comparator

Twice-daily regimen of immediate release tacrolimus, mycophenolate mofetil (MMF)/mycophenolic acid (MPA) plus daily methylprednisolone or prednisone.

干预措施: Induction Immunosuppression with Basiliximab or Rabbit Anti Thymoglobulin (rATG) (Drug)

Twice-daily Regimen

Active Comparator

Twice-daily regimen of immediate release tacrolimus, mycophenolate mofetil (MMF)/mycophenolic acid (MPA) plus daily methylprednisolone or prednisone.

干预措施: Twice-daily Tacrolimus (Drug)

结局指标

主要结局

To compare the composite incidence of biopsy proven acute rejection, graft survival and patient survival

时间窗: 12 months

Biopsies will be performed for unexplained rise in serum creatinine or proteinuria and the development of donor specific antibodies. Biopsies will be assessed by a pathologist using standard Banff classification of renal allograft pathology. Graft loss will be defined as return to chronic dialysis or graft removal.

次要结局

  • Cancer(3, 6, and 12 months)
  • Diabetes(3, 6, and 12 months)
  • Renal allograft function(Every month, for a duration of 12 months)
  • Proteinuria(Every month, for a duration of 12 months)
  • Donor-specific antibodies (DSA)(3, 6, and 12 months)
  • Cytomegalovirus (CMV)(3, 6, and 12 months)
  • Liver Function(3, 6, and 12 months)
  • Gastrointestinal side effects(3, 6, and 12 months)
  • Dyspepsia and quality of life(3, 6, and 12 months)
  • Tremor(3, 6, and 12 months)
  • Perception of quality of life(3, 6, and 12 months)
  • Electrolytes(3, 6, and 12 months)
  • Adverse Events(3, 6, and 12 months)
  • Dose changes(3, 6, and 12 months)
  • BK Viremia(3, 6, 12 months)

研究者

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

Santhi Voora

Assistant Professor

University of Southern California

研究点 (1)

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