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临床试验/EUCTR2017-002644-32-EE
EUCTR2017-002644-32-EE进行中(未招募)1 期

A Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Study to Demonstrate the Effects of Sotagliflozin on Cardiovascular and Renal Events in Patients with Type 2 Diabetes, Cardiovascular Risk Factors and Moderately Impaired Renal Function

exicon Pharmaceuticals, Inc.0 个研究点目标入组 16,154 人开始时间: 2017年11月2日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
16,154

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

  • -Type 2 Diabetes Mellitus with glycosylated hemoglobin (HbA1c) = 7%.
  • -Estimated glomerular filtration rate (eGFR) = 25 and = 60 mL/min/1.73 m2.
  • -Age 18 years or older with at least one major cardiovascular risk factor or age 55 years or older with at least two minor cardiovascular risk factors.
  • -Signed written informed consent..
  • 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 9700
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 6454

排除标准

  • -Antihyperglycemic treatment has not been stable within 12 weeks prior to screening.
  • -Planned coronary procedure or surgery after randomization.
  • -Lower extremity complications (such as skin ulcer, infection, osteomyelitis, and gangrene) identified during screening and requiring treatment at randomization.
  • -Planning to start a sodium-glucose linked transporter-2 (SGLT2) inhibitor during the study.

研究者

发起方
exicon Pharmaceuticals, Inc.

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Effect of Sotagliflozin on Cardiovascular and Renal... | 临床试验