ENCRT-103-hPI: Evaluation of an Immune-protected ENCRT-103-hPI Containing Primary Human Islets in Adults With Type 1 Diabetes, With and Without Standard-of-care Portal Vein Islet Infusion.
Evaluation of ENCRT-103-hPI, an Immune-protected Combination Product Containing Primary Human Islets in Adults With Type 1 Diabetes, With and Without Standard-of-care Portal Vein Islet Infusion.
研究概览
地位
条件
详细说明
This study is a dual-arm, three-centre, non-randomized, FIH trial that will evaluate the safety of the ENCRT-103-hPI in patients with T1D. Study subjects may be receiving standard of care islet infusion (cohort A), or not (cohort B). Cohort B will receive a different drug regimen compared to cohort A's standard of care immune management.
Both cohorts will experience equivalent processes: donor matching, comparable ENCRT-103-hPI dosages, implant into the upper arm or abdomen, explant at 4 mo and post surgical followup.
The primary objective is to evaluate the safety, tolerability, and local tissue response of fully immune-protected ENCRT devices containing primary human islets in adults with Type 1 Diabetes. Included in assessments are vascular integration and immune cell exclusion.
The secondary objectives are to evaluate of the activity, function, and survival of the donor islets from the retrieved ENCRT-103-hPI.
The exploratory objectives include measures of circulating and stimulated C-peptide, HbA1c, insulin use doses, and when available, CGM trends.
研究类型
注册 (估计的)
阶段
- 阶段1
联系人和位置
学习地点
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British Columbia
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Vancouver、British Columbia、加拿大
- Vancouver General Hospital
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首席研究员:
- Michael Bleszynski, MD
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Ontario
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Toronto、Ontario、加拿大
- UHN
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首席研究员:
- Trevor Reichman, MD
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接触:
- Site coordinator, DDM
- 电话号码:416-340-4800
- 邮箱:honey.lad@uhn.ca
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-
参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
- follows those of the institutions' standard of care (cohort A) or care team's guidelines (cohort B).
Exclusion Criteria:
- - follows those of the institutions' standard of care (cohort A) or care team's guidelines (cohort B).
学习计划
研究是如何设计的?
设计细节
- 主要用途:设备可行性
- 分配:非随机化
- 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 |
|---|---|
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实验性的:Cohort A: ENCRT-103-hPI with standard of care
Patients receive standard of care islet infusion and the intervention of an ENCRT implant on the same day.
Cohort A also receives standard of care drug regimen for immune management.
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The ENC-103-CED is a unique device on the landscape. It is a soft, device made of non-fibrosis inducing material and design features. ENCRT-103-hPI that will be implanted consists of this device loaded with primary islets. Both cohorts A and B will receive the intervention of an ENCRT-103-hPI implant.
其他名称:
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实验性的:Cohort B: ENCRT-103-hPI only
Patients receive only an ENCRT implant (the intervention) and a drug for engraftment and immune management.
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The ENC-103-CED is a unique device on the landscape. It is a soft, device made of non-fibrosis inducing material and design features. ENCRT-103-hPI that will be implanted consists of this device loaded with primary islets. Both cohorts A and B will receive the intervention of an ENCRT-103-hPI implant.
其他名称:
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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 |
|---|---|---|
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Rate of device-related adverse events (AEs)
大体时间:4.5-5 months
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The primary objective is to evaluate the safety, tolerability, and local tissue response of fully immune-protected ENCRT devices containing primary human islets in adults with Type 1 Diabetes.
Included in assessments are vascular integration and immune cell exclusion.
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4.5-5 months
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Assessment of IEQ (islet equivalent) population present in explants
大体时间:4 months
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The secondary objectives are to evaluate of the activity, function, and survival of the donor islets from the retrieved ENCRT-103-hPI through marker expression in histological sections.
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4 months
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其他结果措施
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Exploratory functional outcomes
大体时间:4 months
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Characterize potential functional engraftment via device removal and fixation for histopathological analysis (post-explant).
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4 months
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合作者和调查者
赞助
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他研究编号
- ENCRT-103-hPI
- 2-IND-2026-1973-I-X (其他赠款/资助编号:Breakthrough T1D)
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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