A Prospective Cohort Study of Operationally Tolerant Allograft Recipients (ITN063ST)
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 41
- 试验地点
- 5
- 主要终点
- Time to Loss of Operational Tolerance
研究概览
简要总结
Antirejection medicines, also known as immunosuppressive drugs, are prescribed to organ transplant recipients to prevent their bodies from rejecting the new organ. Some organ transplant recipients can stop taking anti-rejection medicines without rejecting their transplanted organ (this is called 'tolerance'). The purpose of this study will collect samples and data from 'tolerant' liver or kidney transplant recipients in order to find out:
The purpose of this study is to collect samples and data in order to find out:
- How long liver or kidney transplant recipients can remain tolerant;
- What happens in the tolerant recipient's body over time; and
- If there are patterns in the body that are linked to tolerance.
详细描述
This is a multi-center, prospective, observational study in which operationally tolerant recipients of liver or kidney allografts will be followed longitudinally, with annual collections of clinical data and biological samples. All participants will be followed for the duration of the study, regardless of changes in their tolerance status.
Participants will be recruited by three main pathways:
- Tolerant participants from current and past Immune Tolerance Network (ITN) trials, including those who have already completed trial participation and those who are anticipated to complete trial participation,
- Tolerant participants referred by ITN affiliated investigators, academic and community transplant physicians and directly through outreach to transplant affinity groups such as the National Kidney Foundation (NKF), and
- Tolerant participants from the general transplant community who are reachable through general contact channels such as the ITN website, word-of-mouth referrals from existing participants, and social media.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Recipient of single organ liver or kidney allograft from a living or deceased donor;
- •At screening, operationally tolerant, as defined by:
- •Absence of any immunosuppressive therapy for ≥52 weeks prior to the screening visit, and
- •No evidence of allograft rejection in the 52 weeks prior to the screening visit, based on the allograft recipient's medical history.
- •Normal allograft function, defined as:
- •For liver transplant recipients: Liver function tests (ALT, GGT) both less than or equal to the upper limit of normal (ULN); and,
- •For kidney transplant recipients: Serum creatinine value corresponds to an estimated GFR > 45 ml/min/1.73 m^
- •Receiving regular follow-up for a kidney or liver transplant by a local physician:
- •-Participants must be willing to allow the study team to contact and share medical information with this local physician.
- •Ability to sign informed consent.
排除标准
- •Current malignancy requiring recent surgery, ongoing chemotherapy, or radiation;
- •Transplant of another organ;
- •Current drug or alcohol dependency;
- •Any medical condition that in the opinion of the principal investigator would interfere with safe completion of the trial; and
- •Inability to comply with the study visit schedule and required assessments.
结局指标
主要结局
Time to Loss of Operational Tolerance
时间窗: From operational tolerance to ITN063ST study completion, assessed up to 60 months
A participant is considered to have operational tolerance if they are off all immunosuppression medication while continuing to have stable allograft function and no rejection. For these participants, the date of operational tolerance is considered as 52 weeks from the participant's last documented dose of immunosuppression. A participant will be considered to have lost operational tolerance if they experience rejection, have loss of stable allograft function (in the absence of confounding factors), or restart immunosuppression. The endpoint was analyzed using Kaplan-Meier survival estimate and associated two-sided 95% confidence interval, using a delayed-entry model with left-truncation of survival times by censoring the time from achieving operational tolerance at the time of study enrollment. The survival estimate is at the time of the last of event.
次要结局
- Number of Participants With Graft Loss, Not Including Death With a Functioning Graft(Day 0 (Study Enrollment) to Study Completion (Up to 3.7 years))
- Time to Development of Anti-Human Leukocyte Antigen (HLA) Antibody or Donor Specific Antibodies (DSA)(Day 0 (Study Enrollment) to Study Completion (Up to 3.7 years))
- Number of Participants With Biopsy-Proven or Clinical Acute Rejection, Steroid Resistant Rejection and/or Chronic Rejection(Day 0 (Study Enrollment) to Study Completion (Up to 3.7 years))