NCT02131246已完成1 期
A Randomised Trial Investigating the Pharmacokinetic and Pharmacodynamic Properties of Faster-acting Insulin Aspart in Subjects With Type 1 Diabetes
适应症
干预措施
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 33
- 试验地点
- 1
- 主要终点
- Mean plasma glucose concentration
研究概览
简要总结
This trial is conducted in Europe. The aim of the trial is to investigate the pharmacokinetic (the exposure of the trial drug in the body) and pharmacodynamic (the effect of the investigated drug on the body) properties of faster-acting insulin aspart in subjects with Type 1 diabetes.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 64 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Male or female 18-64 years (both inclusive) at the time of signing informed consent
- •Type 1 diabetes mellitus (as diagnosed clinically) for at least 12 months
- •Body mass index 18.5-28.0 kg/m^2 (both inclusive)
排除标准
- •Subject who has donated any blood or plasma in the past month or more than 500 mL within 3 months prior to screening
- •Smoker (defined as a subject who is smoking at least one cigarette, cigar or pipe daily)
研究组 & 干预措施
Faster-acting insulin aspart
Experimental
Each subject will be allocated to two treatments (in random sequence).
干预措施: Faster-acting insulin aspart (Drug)
NovoRapid®
Active Comparator
Each subject will be allocated to two treatments (in random sequence).
干预措施: insulin aspart (Drug)
结局指标
主要结局
Mean plasma glucose concentration
时间窗: From 0-6 hours after start of a standardised meal
次要结局
- Area under the serum insulin aspart concentration-time curve(From 0 to 12 hours after trial product administration)
研究者
研究点 (1)
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