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临床试验/EUCTR2015-001702-33-ES
EUCTR2015-001702-33-ES进行中(未招募)1 期

A 24-week International, Multicenter, Randomized, Open-Label, Active-Controlled, Parallel Group, Phase 3b Trial with a 28-week Extension to Evaluate the Efficacy and Safety of Saxagliptin Co-administered with Dapagliflozin Compared to Insulin Glargine in Subjects with Type 2 Diabetes who have Inadequate Glycemic Control on Metformin with or without Sulfonylurea Therapy

AstraZeneca AB0 个研究点目标入组 598 人开始时间: 2015年11月5日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
598

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • ? Males and females aged ? 18 years old at the time of screening visit.
  • ? Subjects with T2DM with inadequate glycemic control, defined as a central laboratory HbA1c ? 8 % and ? 12 % obtained at the screening visit.
  • ? Note: At Week -2 (Lead-In), a central laboratory fasting plasma glucose (FPG) qualification check will be performed. Subjects will only be randomized on Day 1 if their FPG is ? 270 mg/dL (15 mmol/L) at the Week -2 qualification check. A re-test will be permitted within (7) days if the Week -2 central lab FPG result was > 270mg/dL (15 mmol/L) but < 300 mg/dL (16.6 mmol/L). Subjects will be excluded if the central lab FPG value at Week -2 (Lead-In) is ? 300 mg/dL (16.6 mmol/L) or if the central lab FPG value at Week -2 (Lead-In) and the re-test FPG value are both > 270 mg/dL (15 mmol/L).
  • ? Subjects must be taking a stable dose of metformin ? 1500 mg/day for at least 8 weeks prior to screening visit with or without a stable dose of SU of at least 50% maximal dose per local label for at least 8 weeks prior to screening visit. Subjects must not take any other antidiabetic therapy for more than 14 days (consecutive or not) during 12 weeks prior to screening.
  • ? BMI ? 45.0 kg/m2 at the screening visit.
  • ? Women of childbearing potential (WOCBP) must have a negative serum or urine pregnancy test (minimum sensitivity 25 IU/L or equivalent units of HCG) at screening and within 24 hours prior to the start of study drug.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 478
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 120

排除标准

  • ? Clinical diagnosis of Type 1 Diabetes.
  • ? History of unstable or rapidly progressing renal disease, hepatic insufficiency or current, acute or chronic pancreatitis.
  • ? Any of the following cardiovascular/vascular diseases within 3 months of enrollment visit: MI, CABG, PTCA, valvular disease or repair, unstable angina or unstable CHF, TIA, Class III or IV heart failure, known left ventricular ejection fraction of < 40%, or significant cerebrovascular disease.
  • ? Impairment of renal function (defined as creatinine clearance [CrCl] < 60 mL/min [estimated by Cockcroft-Gault] or serum creatinine [SCr] ? 1.5 mg/dL in males or ? 1.4 mg/dL in females).
  • ? Hematuria (confirmed by microscopy at screening) with no explanation as judged by the investigator up to randomization. If bladder cancer is identified, subjects are not eligible to participate.
  • ? Hematological or oncological diseases or conditions.
  • ? Participation in a commercial weight loss program or history of bariatric surgery.
  • ? Replacement or chronic systemic corticosteroid therapy.
  • ? Administration of any other investigational drug or participation in any interventional clinical study within (30) days prior to screening for this study.

研究者

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