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临床试验/NCT02229396
NCT02229396已完成3 期

A 28-week, Multicenter, Randomized, Double-Blind, Active-Controlled, Phase 3 Study With a 24-week Extension Phase Followed by a 52-week Extension Phase to Evaluate the Efficacy and Safety of Simultaneous Administration of Exenatide Once Weekly 2 mg and Dapagliflozin Once Daily 10 mg Compared to Exenatide Once Weekly 2 mg Alone and Dapagliflozin Once Daily 10 mg Alone in Patients With Type 2 Diabetes Who Have Inadequate Glycemic Control on Metformin

AstraZeneca1 个研究点 分布在 1 个国家目标入组 695 人开始时间: 2014年9月4日最近更新:
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
695
试验地点
1
主要终点
Change in HbA1c From Baseline to Week 28

研究概览

简要总结

Study D5553C0003 is a 28-week, randomized, double-blind, active-controlled, multicenter, Phase 3 efficacy and safety study with 24-week and 52-week extension phases of simultaneous administration of exenatide once weekly (EQW) 2 mg and dapagliflozin 10 mg once daily (QD) compared to EQW 2 mg alone and dapagliflozin 10 mg QD alone in patients with Type 2 diabetes who have inadequate glycemic control on metformin.

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
18 Years 至 130 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Exenatide Once Weekly 2 mg and Dapagliflozin Once Daily 10 mg

Experimental

干预措施: Exantide with Dapagliflozin (Drug)

Exenatide Once Weekly 2 mg Alone

Experimental

干预措施: Exentide (Drug)

Dapagliflozin Once Daily 10 mg Alone

Active Comparator

干预措施: Dapagliflozin (Drug)

结局指标

主要结局

Change in HbA1c From Baseline to Week 28

时间窗: Baseline to Week 28

To compare the change from baseline to Week 28 in HbA1c between exenatide once weekly (EQW) 2 mg and dapagliflozin 10 mg administered simultaneously compared to EQW 2 mg alone and dapagliflozin 10 mg alone.

次要结局

  • Change in Body Weight From Baseline to Week 28(Baseline to Week 28)
  • Change in Fasting Plasma Glucose From Baseline to Week 2(Baseline to Week 2)
  • Percentage of Patients Achieving HbA1c <7% at Week 28(Baseline to Week 28)
  • Change in Systolic Blood Pressure From Baseline to Week 28(Baseline to Week 28)
  • Change in Fasting Plasma Glucose From Baseline to Week 28(Baseline to Week 28)
  • Change From Baseline to Week 28 in 2-hour Postprandial Glucose After a Standard Meal Tolerance Test(Baseline to Week 28)
  • Percentage of Patients Achieving Weight Loss ≥5.0% at Week 28(Baseline to Week 28)

研究者

发起方
AstraZeneca
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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