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临床试验/NCT04614142
NCT04614142撤回4 期

Single Patient Protocol for Donor HCV-positive to Recipient HCV-negative Kidney Transplant in a Patient at Risk for Loss of Dialysis Access

Massachusetts General Hospital1 个研究点 分布在 1 个国家开始时间: 2020年11月13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
撤回
试验地点
1
主要终点
Hepatitis C viral load (RNA)

研究概览

简要总结

This is a single patient, single center study evaluating if administration of pan-genotypic DAA therapy on day 3 (+/- 2 days) post-kidney transplant prevents the transmission of hepatitis C virus infection from an HCV-positive donor kidney to an HCV-negative recipient.

详细描述

The patient selected for this study previously received a kidney transplant under protocol 2016P002051. Unfortunately, she experienced primary graft nonfunction due to a renal vein thrombus and acute thrombotic microangiopathy and the transplanted HCV+ kidney was removed. She continued glecaprevir and pibrentasvir for the full course (8 weeks of treatment) and was cured of HCV. However, she continues on dialysis requiring ongoing, albeit low dose, immunosuppression after her failed transplant. This causes increased risk of infection and other dialysis-related morbidity. Futhermore, she is at risk of access loss due to multiple failed fistula attempts and prior dialysis catheter line thrombosis. Of note, she also failed a trial of peritoneal dialysis due to development of a large pleural effusion (a known treatment-limiting complication of peritoneal dialysis). Thus, this young patient, is at risk of losing dialysis access which could lead to death. The MGH transplant team has now decided that she could be retransplanted with alterations in peri-transplant anticoagulation and immunosuppression (eculizumab) that they are confident should decrease her risk of peri-transplant thrombosis and recurrent TMA. Thus, we desire to expedite her access to re-transplant. Through this protocol, this recipient will be given the opportunity to accept a kidney that is HCV antibody positive and nucleic acid test (NAT) negative or HCV NAT positive and will be treated with oral glecaprevir (300mg)/pibrentasvir (120mg) (G/P, MavyretTM) on day 3 (+/- 2 days) post-kidney transplant to prevent the transmission of HCV infection at the time of transplant. Our goal is to provide access to kidney transplantation as soon as possible, with a donor of any genotype of infection, with elimination of the potential HCV infection by therapy used on day 3 (+/- 2 days) in the case of HCV NAT+ transplant and surveillance and reactive therapy in the case of HCV antibody positive NAT- transplant.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
34 Years 至 44 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Detectable HCV Antibody Positivity
  • KDPI score is less than ≤ 0.650
  • Traditional Donor Selection Criteria Met - acceptable for transplantation per usual evaluation at MGH
  • Donor exclusion criteria
  • Donor has been known to have previously received and failed HCV treatment with a direct-acting antiviral agent
  • Confirmed HIV
  • Confirmed HBV positive (surface antigen or HBV DNA positive)
  • Kidney anatomical damage or significant pathology noted during recovery
  • Significant liver disease or signs of liver decompensation (splenomegaly, ascites) noted during recovery (advanced fibrosis or cirrhosis)
  • Any standard contra-indication to donation noted in donor (significant malignancy, unusual infection)
  • Recipient Inclusion/Exclusion Criteria
  • Previously enrolled in IRB 2016P002051 and experienced primary graft nonfunction due to renal vein thrombosis and acute thrombotic microangiopathy
  • Willing and able to sign informed consent

排除标准

  • 未提供

研究组 & 干预措施

Experimental: Glecaprevir/pibrentasvir for HCV+ kidney transplant recipient

Experimental

Glecaprevir (100mg) / pibrentasvir (40mg) (fixed dose combination) treatment for Hepatitis C virus (HCV)-naive recipients who receive a kidney transplant from a deceased, HCV-infected donor.

Subject will receive first dose on day 3 (+/- 2 days) post-kideny transplantation and continue daily for 8 weeks.

干预措施: Glecaprevir / Pibrentasvir Oral Tablet [Mavyret] (Drug)

结局指标

主要结局

Hepatitis C viral load (RNA)

时间窗: 20 weeks post-transplant (12-weeks post-treatment)

Negative hepatitis C viral load (RNA) tested using PCR at 12 weeks post-treatment (SVR12)

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

Raymond Chung

Director of Hepatology and Liver Center

Massachusetts General Hospital

研究点 (1)

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