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临床试验/NCT00698932
NCT00698932已完成3 期

A 24-Week International, Multi-centre, Randomized, Parallel-group, Double-blind, Placebo-controlled, Phase III Study to Evaluate the Efficacy and Safety of Saxagliptin in Adult Patients With Type 2 Diabetes Who Have Inadequate Glycaemic Control With Diet and Exercise.

AstraZeneca1 个研究点 分布在 1 个国家目标入组 568 人开始时间: 2008年6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
发起方
AstraZeneca
入组人数
568
试验地点
1
主要终点
Absolute Change From Baseline to Week 24 in Glycosylated Haemoglobin A1c (HbA1c)

研究概览

简要总结

Saxagliptin is a new investigational medication being developed for treatment of type 2 diabetes. This study is designed to evaluate the efficacy and safety in adult patients with inadequate glycaemic control with diet and exercise.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Diagnosed with Type 2 diabetes
  • Patients should be drug naïve ie, not received medical treatment for diabetes,
  • HbA1c ≥ 7.2% and ≤10.0% (at enrolment), HbA1c ≥ 7.0% and ≤10.0% (at randomization)

排除标准

  • Insulin therapy within one year of enrolment (with the exception of insulin therapy during a hospitalization or use in gestational diabetes),
  • Type 1 diabetes,history of ketoacidosis or hyperosmolar non-ketonic koma

研究组 & 干预措施

Saxagliptin 5mg

Experimental

干预措施: Saxagliptin (Drug)

Placebo

Placebo Comparator

干预措施: Placebo (Drug)

结局指标

主要结局

Absolute Change From Baseline to Week 24 in Glycosylated Haemoglobin A1c (HbA1c)

时间窗: Baseline , Week 24

Adjusted\* mean change from baseline in HbA1c achieved with saxagliptin 5 mg versus placebo at week 24 (LOCF, Full Analysis set). HbA1c is a continuous measure, the change from baseline for each subject is calculated as the week 24 values minus the baseline value. HbA1c data were excluded on and after rescue medication.

次要结局

  • Absolute Change (mmol/L) From Baseline to Week 24 in Fasting Plasma Glucose (FPG)(Baseline, Week 24)
  • Absolute Change (mg/dL) From Baseline to Week 24 in Fasting Plasma Glucose (FPG)(Baseline, Week 24)
  • Absolute Change (mmol*Min/L) From Baseline to Week 24 in Area Under the Curve (AUC) From 0 to 180 Minutes for Postprandial Glucose (PPG) During Mixed Meal (Instant Noodles) Tolerance Tests (MMTT) in All MMTT Participants(Baseline , Week 24)
  • Absolute Change (mg*Min/dL) From Baseline to Week 24 in Area Under the Curve (AUC) From 0 to 180 Minutes for Postprandial Glucose (PPG) During Mixed Meal (Instant Noodles) Tolerance Tests (MMTT) in All MMTT Participants(Baseline , Week 24)
  • Proportion of Patients Achieving a Therapeutic Glycemic Response Defined as HbA1c <7.0% at Week 24(Baseline, Week 24)

研究者

发起方
AstraZeneca
申办方类型
Industry

研究点 (1)

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