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临床试验/NCT02324842
NCT02324842已完成不适用

Effect of Combined Incretin-Based Therapy Plus Canagliflozin on Glycemic Control and the Compensatory Rise in Hepatic Glucose Production in Type 2 Diabetic Patients

The University of Texas Health Science Center at San Antonio1 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2014年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
45
试验地点
1
主要终点
HbA1c at 4 Months

研究概览

简要总结

Specific Aim 1.To examine whether the combination of liraglutide plus canagliflozin can prevent the increase in Hepatic Glucose Production (HGP) following institution of canagliflozin therapy and produce an additive or even synergistic effect to lower the plasma glucose concentration and A1c.

Specific Aim 2: To examine whether combination therapy with liraglutide plus canagliflozin can produce an additive, or even synergistic, effect to promote weight loss and reduction in hepatic and visceral fat content.

Specific Aim 3. To examine whether combination therapy with liraglutide plus canagliflozin can produce an additive or even synergistic effect to reduce systolic/diastolic blood pressure and 24-hour integrated blood pressure.

详细描述

Specific Aim 1.To examine whether the combination of liraglutide plus canagliflozin can prevent the increase in HGP following institution of canagliflozin therapy and produce an additive or even synergistic effect to lower the plasma glucose concentration and A1c. We will examine this hypothesis by comparing the effect of administration of liraglutide alone, canagliflozin alone, and the combination of liraglutide plus canagliflozin on:(i) the rate of HGP; (ii) decrease in fasting plasma glucose concentration; (iii) counter-regulatory hormone response and (iv) A1c. We anticipate that the addition of liraglutide to canagliflozin will prevent the increase in plasma glucagon concentration, augment insulin secretion, and blunt/block the increase in HGP in response to canagliflozin, resulting in a greater decrease in fasting plasma glucose concentration and A1c than observed with each therapy alone.

Specific Aim 2: To examine whether combination therapy with liraglutide plus canagliflozin can produce an additive, or even synergistic, effect to promote weight loss and reduction in hepatic and visceral fat content.

Specific Aim 3. To examine whether combination therapy with liraglutide plus canagliflozin can produce an additive or even synergistic effect to reduce systolic/diastolic blood pressure and 24-hour integrated blood pressure.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male and female subjects between the ages of 18-70
  • Subjects with Type 2 Diabetes Mellitus (T2DM)
  • Drug naïve or on stable dose (more than 3 months) of metformin with or without sulfonylurea
  • Have an HbA1c levels ≥7.0% and <10.0%
  • Stable weight (± 3 lbs) over the preceding 3 months

排除标准

  • Subjects taking drugs known to affect glucose metabolism (other than metformin) will be excluded.
  • Individuals with evidence of proliferative diabetic retinopathy or plasma creatinine >1.4 females or >1.5 males or estimated Glomerular Filtration Rate (eGFR)< 60 ml/min.172m2 will be excluded
  • Unstable body weight (change of greater than ±3 lbs over the preceding 3 months)
  • Participates in excessively heavy exercise program

研究组 & 干预措施

Canagliflozin

Active Comparator

canagliflozin (film-coated tablet), 100 mg/day, increased to 300 mg/day after week two if tolerated without side effects

干预措施: Canagliflozin (Drug)

liraglutide

Active Comparator

liraglutide, 1.2 mg/day, increased to 1.8 mg/day after week two if tolerated without side effects

干预措施: Liraglutide (Drug)

canagliflozin plus liraglutide

Active Comparator

canagliflozin, 100 mg/day, plus liraglutide, 1.2 mg/day, increased to 300 mg/day and 1.8 mg/day, respectively at week two, if tolerated without side effects

干预措施: Canagliflozin (Drug)

canagliflozin plus liraglutide

Active Comparator

canagliflozin, 100 mg/day, plus liraglutide, 1.2 mg/day, increased to 300 mg/day and 1.8 mg/day, respectively at week two, if tolerated without side effects

干预措施: Liraglutide (Drug)

结局指标

主要结局

HbA1c at 4 Months

时间窗: Approximately 4 months

Primary end point of the study is the HbA1c level in response to canagliflozin alone, liraglutide or canagliflozin with liraglutide.

Fasting Plasma Glucose (FPG) at 4 Months

时间窗: Baseline to Approximately 4 months

Values will be presented as the mean + (Standard Deviation) SD. The difference in HGP and all secondary endpoints at study end versus baseline will be calculated and compared between each active treatment group with ANOVA.

次要结局

  • Body Mass Index (BMI) at 4 Months(Approximately 4 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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