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临床试验/NCT02659891
NCT02659891已完成1 期

Immunoglobulin (Privigen®) Therapy to Treat BK Viremia and Prevent Alloimmune Activation in Kidney Transplant Recipients

Massachusetts General Hospital4 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2016年5月最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
16
试验地点
4
主要终点
BK Viremia

研究概览

简要总结

The overall goal of this study is to rapidly improve clearance of BK viremia with Immunoglobulin (Privigen®) thereby decreasing the potential for formation of alloantibodies in renal transplant recipients that have had immunosuppression reduction due to BK viremia. Our approach is to perform a prospective, randomized, placebo controlled trial intravenous immune globulin (IVIg; Privigen®) plus protocolized immunosuppression reduction versus placebo and protocolized immunosuppression reduction in patients with BK viremia post-kidney transplantation.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Voluntary written informed consent before performance of any study-related procedure not part of normal medical care, with the understanding that consent may be withdrawn by the subject at any time without prejudice to future medical care.
  • Female subject is either postmenopausal for at least 1 year before the screening visit, is surgically sterilized or if they are of childbearing potential, agree to practice effective methods of contraception from the time of signing the informed consent form through 30 days after the last dose of intravenous immune globulin, or agree to completely abstain from heterosexual intercourse.
  • Kidney transplant recipients (living and deceased donors) with new onset BK viremia (defined as BKV plasma DNA load >1000 copies/mL by real-time PCR within 2 weeks of enrollment). For values >5000 copies/mL repeat testing is not required. For values ≤5000 copies/mL repeat testing should be performed to confirm viremia before enrollment.
  • Immunosuppression therapy at enrollment with tacrolimus, MPA, +/- prednisone.
  • Men and Women 18 to 75 years of age.

排除标准

  • Absence of a DQ mismatch to the donor.
  • Patient had known HLA antibodies directed to the donor antigens (pre-formed DSA) prior to transplant.
  • Known to be positive for donor specific anti-HLA antibodies (IgG) at time of enrollment from the most recently drawn sample. (DSA MFI>1000 is considered positive). DSA is detected via center's standard of care testing. If center does not routinely screen then patient may still be enrolled.
  • History of biopsy proven acute rejection (cellular or antibody) at any time prior to enrollment.
  • BKV plasma DNA viral load >300,000 copies/ml.
  • Patient who have received intravenous immune globulin for any reason within 1 month prior to enrollment.
  • Patient with an estimated glomerular filtration rate (MDRD) ≤ 30 ml/min at time of study entry.
  • Patient with selective IgA deficiency or have known antibodies to IgA.
  • Patient with history of hyperprolinemia.
  • Patient with a previous history of a severe systemic or anaphylactic response to intravenous immune globulin.
  • Female subject is pregnant or lactating.
  • Current HCV positivity (by PCR).
  • History of HBsAg-positive.
  • Patients who are HIV-positive.
  • Recipients of a kidney from a donor who tests positive for HIV or HBsAg
  • Participation in clinical trials with other investigational agents not included in this trial, within 14 days of the start of this trial and throughout the duration of this trial.
  • Inability to perform follow-up or to undergo renal allograft biopsy.
  • Serious medical or psychiatric illness likely to interfere with participation in this clinical study.

结局指标

主要结局

BK Viremia

时间窗: 3 Months

Resolution of BK viremia by 3 months post-enrollment. Resolution is defined as a decrease in viral load of BKV in the plasma to \<1000 copies/mL.

次要结局

  • BK Nephropathy(12 Months)
  • Acute Antibody Mediated Rejection(12 Months)
  • Donor specific anti-HLA antibodies(12 Months)
  • Kidney graft survival(12 Months)
  • Acute Cellular Rejection(12 Months)
  • Interstitial Fibrosis or Transplant Glomerulopathy(12 Months)
  • Glomerular Filtrition Rate (GFR)(12 Months)
  • BKV remission(Up to 24 Months)

研究者

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

Hannah Gilligan

Transplant Nephrologist

Massachusetts General Hospital

研究点 (4)

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