跳至主要内容
临床试验/NCT03183804
NCT03183804已完成不适用

A Follow-up Study to Evaluate the Safety for the Patients With ALLO-ASC-DFU Treatment in Phase 2 Clinical Trial of ALLO-ASC-DFU-201

Anterogen Co., Ltd.4 个研究点 分布在 1 个国家目标入组 54 人开始时间: 2015年12月29日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
54
试验地点
4
主要终点
Number of Participants with Adverse Events as a Measure of Safety and Tolerability

研究概览

简要总结

This is an open-label follow up study to evaluate the safety for the subjects with ALLO-ASC-DFU treatment in phase 2 clinical trial (ALLO-ASC-DFU-201) for 23 months.

详细描述

This is an open-label follow up study to evaluate the safety for the subjects with ALLO-ASC-DFU treatment in phase 2 clinical trial (ALLO-ASC-DFU-201) for 23 months.

ALLO-ASC-DFU is a hydrogel sheet containing allogenic adipose-derived mesenchymal stem cells. Adipose-derived stem cells have anti-inflammatory effect and release growth factors such as vascular endothelial growth factor (VEGF) and hepatocyte growth factor (HGF), which can enhance wound healing and regeneration of new tissue, finally may provide a new option in treating a Diabetic Foot Ulcer.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects who are treated with ALLO-ASC-DFU sheet in phase 2 clinical trial of ALLO-ASC-DFU-
  • Subjects who are able to give written informed consent prior to study start and to comply with the study requirements.

排除标准

  • Subjects who are considered not suitable for the study by the principal investigator.

结局指标

主要结局

Number of Participants with Adverse Events as a Measure of Safety and Tolerability

时间窗: up to 24 months

Evaluation of AE

次要结局

未报告次要终点

研究者

发起方
Anterogen Co., Ltd.
申办方类型
Industry
责任方
Sponsor

研究点 (4)

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