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临床试验/NCT00396071
NCT00396071已完成3 期

A Single-center, Double-blind, Randomized, Placebo-controlled, Cross-over Study to Assess the Effect of Vildagliptin on the Incretin Effect in Patients With Type 2 Diabetes Treated With Metformin

Novartis Pharmaceuticals2 个研究点 分布在 2 个国家目标入组 22 人开始时间: 2006年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
22
试验地点
2
主要终点
Change in C-peptide IAUC (0-4hr)

研究概览

简要总结

This mechanistic study will evaluate the effect of vildagliptin on glucose-stimulated insulin secretion to improve the incretin effect in patients with type 2 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

入排标准

年龄范围
30 Years 至 78 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with type 2 diabetes on metformin for at least 3 months and have been on a stable dose of at least 1500 mg daily for a minimum of 4 weeks
  • Agreement to maintain the same dose of metformin throughout the study
  • Body mass index (BMI) in the range of 22-35 kg/m2
  • HbA1c in the range of 7.0 to 9.0%
  • FPG <200 mg/dl (11.1 mmol/L)
  • Agreement to maintain prior diet and exercise habits during the full course of the study
  • Ability to comply with all study requirements and signed informed consent to participate in the study

排除标准

  • A history of type 1 diabetes
  • A history of acute metabolic diabetic complications
  • Evidence of significant diabetic complications
  • Insulin treatment for longer than 10 days within the past 6 months
  • Treatment with any oral anti-diabetic other than metformin within 3 months prior to visit 1
  • Other protocol-defined inclusion/exclusion criteria may apply

研究组 & 干预措施

1

Experimental

Vildagliptin 100 mg qd

干预措施: vildagliptin (Drug)

2

Placebo Comparator

Matching placebo

干预措施: Placebo (Drug)

结局指标

主要结局

Change in C-peptide IAUC (0-4hr)

时间窗: 2 weeks after treatment

次要结局

  • Change in postprandial insulin(after two weeks of treatment)
  • Change in postprandial GLP-1(after 2 weeks of treatment)
  • Change in insulin secretion rate (ISR) relative to glucose (0-2hr)(after 2 weeks of treatment)
  • Change in postprandial C-peptide(after two weeks of treatment)
  • Change in postprandial glucagon(after two weeks of treatment)

研究者

申办方类型
Industry

研究点 (2)

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