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临床试验/NCT00931476
NCT00931476已完成1 期

A Single-centre, Randomised, Double-blind, Placebo-controlled, Parallel Group, Single Dose Trial in Healthy Caucasians and Japanese Subjects Investigating the Pharmacokinetics of Norditropin® (Norditropin® PenSet® 24)

Novo Nordisk A/S2 个研究点 分布在 1 个国家目标入组 86 人开始时间: 2000年4月6日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
86
试验地点
2
主要终点
Area under the hGH concentration-time curve (GH AUC0-24h)

研究概览

简要总结

This trial was conducted in the United States of America (USA). The aim of this clinical trial was to investigate the pharmacokinetics of somatropin in healthy Japanese and Caucasian subjects, and to identify somatostatin-related adverse events.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
20 Years 至 50 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • Signed informed consent before any trial related activities
  • Japanese and Caucasian males respectively
  • Healthy subjects based upon medical history, physical examination, vital signs, ECG, serum biochemistry and haematology and urinalysis
  • Body Mass Index (BMI) between 17 and 30 m2/kg, inclusive

排除标准

  • 未提供

结局指标

主要结局

Area under the hGH concentration-time curve (GH AUC0-24h)

时间窗: from 0 to 24 hours following injection

Treatment Emergent Adverse Events

时间窗: from 0 to 24 hours following injection

Maximum hGH concentration (GH Cmax)

时间窗: from 0 to 24 hours following injection

次要结局

  • Area under the hGH concentration-time curve GH AUC0-∞)
  • Elimination half-life (GH t½)
  • Non-treatment Emergent Adverse Events
  • Time to maximum hGH concentration (GH tmax)
  • Growth Factors (IGF-I and IGFBP-3)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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