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临床试验/NCT02169531
NCT02169531已完成1 期

Pilot Study of a Cell-Based Therapy for Treatment of Hyperglycemia in Type 2 Diabetes Mellitus

B & Y Technologies2 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2014年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
25
试验地点
2
主要终点
Change from Baseline Hemoglobin A1c (HbA1c) at up to 27 weeks.

研究概览

简要总结

Diabetes mellitus type 2 is a long-term metabolic disorder that is primarily characterized by insulin resistance, relative insulin deficiency and hyperglycemia. Our hypotheses is that liver would be the primary organ responsible for the metabolic disorder because of some unknown defects, where sugar would not be efficiently converted to glycogen and fat, leading to hyperglycemia. The constant hyperglycemia would keep pressure on beta-cells in the pancreas to eventually exhaust their ability to produce and secret sufficient amount of insulin, exacerbating the disease. The Immunotherapy would enhance the liver functions and correct the abnormal sugar metabolism. In addition, the ex vivo activated cells produce and secret growth factors which would help endothelial cells of blood vessels to reproduce and grow, resulting in reduced arteriosclerosis.

详细描述

We plan to recruit 20 patients with type 2 diabetes mellitus who suffer hyperglycemia with or without medication. The patients will come to our hospitals for the treatment. A small amount of peripheral blood will be drawn and processed and cultured in our laboratory. The cultured cells (autologous) will be infused intravenously back to patients. Levels of plasma hemoglobin A1c (HbA1c) and other metabolic parameters before and after the therapy will be compared. The therapy is planned to take four weeks for each patient.

研究设计

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

入排标准

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

入选标准

  • Patients diagnosed with type 2 diabetes mellitus.
  • 25 years of age or older. Both sexes.
  • HbA1c ≧6.5% for more than 6 months with or without medication.
  • Capability of providing informed consent.

排除标准

  • History of malignancy.
  • Patients with active infections.
  • Seropositivity for HIV infection.
  • History of myocardial infarction or unstable angina in the previous 3 months.
  • Pregnancy or nursing.

研究组 & 干预措施

ex vivo activated immune cells

Experimental

Up to 20 patients diagnosed with type 2 diabetes mellitus and hyperglycemia will be enrolled and assigned to a single treatment group. Patients will give a small amount of peripheral blood and the blood will be processed and cultured in our laboratory. The ex vivo activated autologous blood cells will be infused intravenously back to patients. The treatment will be done twice a week for consecutive 4 weeks. The metabolic parameters of patients before and after the therapy will be compared to determine if the therapy is safe and effective.

干预措施: ex vivo Activated Immune Cells (Drug)

结局指标

主要结局

Change from Baseline Hemoglobin A1c (HbA1c) at up to 27 weeks.

时间窗: Point 1: The week (week 1) before the first cell infusion assessed as the baseline; Point 2: The week (week 6) after the last cell infusion; Point 3 and after: every 4 weeks up to 27 weeks.

次要结局

  • Change from Baseline Lipid Profile at up to 27 weeks.(Point 1: The week (week 1) before the first cell infusion assessed as the baseline; Point 2: The week (week 6) after the last cell infusion; Point 3 and after: every 4 weeks up to 27 weeks.)

研究者

发起方
B & Y Technologies
申办方类型
Industry
责任方
Principal Investigator
主要研究者

Demao Yang

Chief Scientist

B & Y Technologies

研究点 (2)

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