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临床试验/NCT00976495
NCT00976495已完成2 期

An Exploratory Phase 2 Study to Assess the Effect of Dapagliflozin on Glomerular Filtration Rate (GFR) in Subjects With Type 2 Diabetes Who Have Inadequate Glycemic and Blood Pressure (BP) Control

AstraZeneca10 个研究点 分布在 2 个国家目标入组 154 人开始时间: 2009年10月最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
发起方
AstraZeneca
入组人数
154
试验地点
10
主要终点
Adjusted Percent Change From Baseline in Glomerular Filtration Rate (GFR) at Week 12 (Modified Last Observation Carried Forward [MLOCF])

研究概览

简要总结

The purpose of this study is to evaluate the effects of dapagliflozin on kidney function, as assessed by glomerular filtration rate.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Double (Participant, Care Provider)

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

  • Type 2 diabetes and inadequate glycemic control, defined as A1C ≥ 6.6 and ≤ 9.5%
  • Stable dose of metformin AND/OR a sulfonylurea, for at least 4 weeks prior to the enrollment visit
  • Inadequate blood pressure (BP) control, defined as systolic BP (SBP) ≥ 130 and < 165 mmHg, AND/OR diastolic BP (DBP) ≥ 80 and < 105 mmHg
  • C-peptide ≥ 0.8 ng/mL
  • Estimated GFR by the Modification of Diet in Renal Disease (MDRD) formula > 60 mL/min/1.73m² and < 150 mL/min/1.73m²
  • Urine albumin:creatinine ratio (UACR) < 300 mg/g
  • BMI ≤ 45.0 kg/m2

排除标准

  • Administration of diuretics or other medication approved for the treatment of hypertension (with the exception of either ACEI or ARB), at any dose during the 12 weeks prior to the enrollment visit
  • History of adverse reaction to radio-contrast dye
  • Allergy or contraindication to use of thiazide diuretics
  • Aspartate Aminotransferase (AST) > 3X Upper limit of normal (ULN)
  • Alanine aminotransferase (ALT) > 3X ULN
  • Serum Total Bilirubin > 1.5X ULN
  • Serum Creatinine (Scr) ≥ 1.50 mg/dL (133 μmol/l) for men; SCr ≥ 1.40 mg/dL (124 μmol/l) for women
  • Currently unstable or serious cardiovascular, renal, hepatic, hematological, oncologic, endocrine, psychiatric, or rheumatic diseases

研究组 & 干预措施

Dapagliflozin

Experimental

干预措施: Dapagliflozin (Drug)

Dapagliflozin

Experimental

干预措施: Placebo (Drug)

Hydrochlorothiazide

Active Comparator

干预措施: Hydrochlorothiazide (Drug)

结局指标

主要结局

Adjusted Percent Change From Baseline in Glomerular Filtration Rate (GFR) at Week 12 (Modified Last Observation Carried Forward [MLOCF])

时间窗: From Baseline to Week 12

Baseline was defined as the last assessment prior to the start date and time of the first dose of the double-blind study medication. In cases where time of the first dose or time of the assessment was not available, baseline was defined as the last assessment on or prior to the date of the first dose of the double-blind study medication. If no Week 12 measurement was available, the last available post-baseline measurement obtained on or after Day 23 was used regardless of rescue medication. Measurements were obtained during radomization visit, and Week 12 in the double-blind period by a central laboratory.

次要结局

  • Adjusted Mean Change From Baseline in Daytime (0900 to 2100 Hours) Ambulatory Systolic Blood Pressure (ASBP) at Week 12 (Last Observation Carried Forward [LOCF])(From Baseline to Week 12)
  • Adjusted Mean Change From Baseline in Nighttime (0100 to 0600 Hours) Ambulatory Systolic Blood Pressure (ASBP) at Week 12 (Last Observation Carried Forward [LOCF])(From Baseline to Week 12)
  • Adjusted Mean Change From Baseline in 24-Hour Ambulatory Systolic Blood Pressure (ASBP) at Week 12 (Last Observation Carried Forward [LOCF])(From Baseline to Week 12)

研究者

发起方
AstraZeneca
申办方类型
Industry
责任方
Sponsor

研究点 (10)

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