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The Role of interferOn and Complement in SecondAry thRombotic micrioangiOpathy (ROSARIO)

2026年7月14日 更新者:Sofie Dhaese

The Role of interferOn and Complement in SecondAry thRombotic micrioangiOpathy (ROSARIO)

Study rationale: Viral infections, such as CMV, are a risk factor for TA-TMA (transplantation-associated TMA). Viral infections increase interferon (IFN) levels and high IFN levels are associated with thrombotic microangiopathy (TMA). IFNs contribute to TMA pathogenesis through suppression of VEGF transcription. Disruption of the VEGF signalling pathway in the kidney is associated with TMA.

Primary objective: To determine the association between IFN levels and the development of biopsy-proven or clinically diagnosed TA-TMA.

Secondary objective(s): To explore the relationship between complement activation and IFN in patients with TMA.

To explore if high IFN levels are associated with low VEGF-A levels. Endpoint: The study aims to investigate the role of IFN in the pathogenesis of secondary thrombotic microangiopathy (focusing on patients with TA-TMA). It seeks to clarify whether IFN, next to complement dysregulation, is a driver of endothelial damage and TMA in these patients.

研究概览

研究类型

介入性

注册 (估计的)

40

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

Participants eligible for inclusion in this study must meet all of the following criteria:

  1. Voluntary written informed consent of the participant or their legally authorized representative has been obtained prior to any screening procedures
  2. At least 18 years of age at the time of signing the Informed Consent Form (ICF)

Specifically for the patients with TMA (G1 and G4):

  1. Patients after allogeneic or autologous hematopoietic stem cell transplantation (HSCT) OR patients after solid organ transplantation OR patients with DITMA AND
  2. Tissue diagnosis of TMA (pathological diagnosis) OR
  3. Clinical diagnosis of TMA based on the following criteria, with ≥4 out of 6 features fulfilled within 14 days (15,52,53):

    • de novo Coombs negative hemolytic anemia OR (in case of HSCT)

      • failure to achieve transfusion independence despite neutrophil engraftment
      • hemoglobin decline by ≥ 1g/dL
      • new onset transfusion dependence
    • otherwise unexplained de novo thrombocytopenia (< 50 x 109/L) OR a 25% decrease in platelet count OR (in case of HSCT)

      • failure to achieve platelet engraftment despite neutrophil engraftment
      • higher than expected transfusion needs
      • refractory to platelet transfusion *≥50% reduction in platelet count after full platelet engraftment
    • lactate dehydrogenase (LDH) above the upper limit of normal
    • schistocytes (=>2 / high power field (HPF)
    • new onset hypertension OR worsening of existing hypertension requiring additional antihypertensive therapy
    • proteinuria > 1g/g creatinine on a random urine protein-to-creatinine ratio Date of TMA diagnosis = first date when ≥4 out of the 6 features are fulfilled.

Specifically for the group of patients without TMA, with infection (G2):

  1. Patients after allogeneic or autologous hematopoietic stem cell transplantation (HSCT) OR patients after solid organ transplantation AND
  2. Symptomatic viral infection (evaluated by the treating physician).

Specifically for the group of patients without TMA, without infection (G3):

  1. Patients after allogeneic or autologous hematopoietic stem cell transplantation (HSCT) OR patients after solid organ transplantation AND
  2. No symptomatic viral infection (evaluated by the treating physician).

Exclusion Criteria:

Participants eligible for this study must not meet any of the following criteria:

  1. Participant has a personal or family history of aHUS
  2. Participant has a history of malignant hypertension
  3. Participant has a history of active cancer, excluding the haematological cancer for which the patient received the stem cell transplantation (if applicable)
  4. The participant received prior complement inhibition
  5. The participant received prior anti-interferon treatment
  6. If applicable: Female who is pregnant, breast-feeding or intends to become pregnant the following year or is of child-bearing potential and not using an adequate, highly effective contraceptive
  7. Participation in an interventional study with an investigational medicinal product (IMP) or device

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:不适用
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
其他:Patients with HSCT-TMA or SOT-TMA
blood and urine collection
blood sampling at designated time points
urine collection at designated time points
其他:Patients after HSCT or SOT with a viral infection, without TMA
blood and urine collection
blood sampling at designated time points
urine collection at designated time points
其他:Patients after HSCT or SOT without a viral infection, without TMA
blood and urine collection
blood sampling at designated time points
urine collection at designated time points
其他:Patients with drug-induced TMA (DITMA)
blood and urine collection
blood sampling at designated time points
urine collection at designated time points

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Interferon signature
大体时间:Time point 1: baseline Time point 2: up to week 52
6-gene interferon signature
Time point 1: baseline Time point 2: up to week 52
VEGF-A
大体时间:Time point 1: baseline Time point 2: up to week 52
VEGF-A level
Time point 1: baseline Time point 2: up to week 52
Complement analysis (serum)
大体时间:Time point 1: baseline Time point 2: up to week 52
CH50, AP50, C3, C3d, C4 and C5b-9 at timepoint 1 and C5b-9 at time point 2
Time point 1: baseline Time point 2: up to week 52

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年9月1日

初级完成 (估计的)

2031年12月31日

研究完成 (估计的)

2031年12月31日

研究注册日期

首次提交

2026年6月19日

首先提交符合 QC 标准的

2026年7月14日

首次发布 (实际的)

2026年7月15日

研究记录更新

最后更新发布 (实际的)

2026年7月15日

上次提交的符合 QC 标准的更新

2026年7月14日

最后验证

2026年7月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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