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临床试验/NCT01030926
NCT01030926已完成1 期

A Trial Investigating the Pharmacokinetic Properties of NN1250 in Children, Adolescents and Adults With Type 1 Diabetes

Novo Nordisk A/S1 个研究点 分布在 1 个国家目标入组 39 人开始时间: 2009年12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
入组人数
39
试验地点
1
主要终点
Area under the NN1250 concentration-time curve after single dose

研究概览

简要总结

This trial was conducted in Europe. The aim of this clinical trial was to look into the concentration of NN1250 (insulin degludec/insulin 454) in the blood after one injection of NN1250 in children, adolescents and adults 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
Double (Participant, Investigator)

入排标准

年龄范围
6 Years 至 65 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male or female aged 6-65 years (both inclusive)
  • Type 1 diabetes mellitus (as diagnosed clinically) for at least 12 months
  • Body mass index for children: 15.0-20.0 kg/m^2 (both inclusive), for adolescents: 18.0-28.0 kg/m^2 (both inclusive) and for adults maximum 30.0 kg/m^2

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
  • Not able or willing to refrain from smoking during the inpatient period
  • Female of childbearing potential who is pregnant, breast-feeding or intends to become pregnant or is not using adequate contraceptive methods

研究组 & 干预措施

A1, first period

Experimental

干预措施: insulin degludec (Drug)

A2, second period

Active Comparator

干预措施: insulin glargine (Drug)

B1, first period

Active Comparator

干预措施: insulin glargine (Drug)

B2, second period

Experimental

干预措施: insulin degludec (Drug)

结局指标

主要结局

Area under the NN1250 concentration-time curve after single dose

时间窗: 0-72 hours after dosing

次要结局

  • Maximum observed NN1250 concentration after single dose(0-72 hours after dosing)
  • Time to maximum observed NN1250 concentration after single dose(0-72 hours after dosing)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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