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临床试验/NCT03544996
NCT03544996已完成不适用

A Comparison of Injected Insulin Replacement Therapy With A Novel Transdermally Delivered Human Insulin Product

Transdermal Delivery Solutions Corp1 个研究点 分布在 1 个国家目标入组 1 人开始时间: 2017年9月9日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
1
试验地点
1
主要终点
Insulin response

研究概览

简要总结

An Early Feasibility Study of a device formulation to deliver human insulin across intact skin

详细描述

An attempt was made to formulate an insulin product that would complex human insulin in a stable anhydrous solution and when applied to the skin enable the uptake and release of insulin in a brittle T1D patient.

A series of formulations were produced at varing dose strengths and in conjunction with injected insulin products, applied and serum glucose measured to ascertain response and optimize a fomrula to be submitted for IND approval.

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
60 Years 至 61 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • Brittle T1D patient with poor insulin sensitivity requiring more than 3,000 IUs on insulin a day

排除标准

  • High insulin sensitivity
  • well managed serum glucose

结局指标

主要结局

Insulin response

时间窗: 8-24 hours

Measurement of down modulation of serum glucose as measured by a standard blood glucose meter not otherwise attributable to injected insulin

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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