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临床试验/CTRI/2015/04/005671
CTRI/2015/04/005671Other2 期

Efficacy and safety of EGT0001442 compared with placebo in patients with type 2 diabetes mellitus inadequately controlled by diet and exercise and up to one oral anti-diabetes agent - none

Theracos Inc0 个研究点目标入组 300 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
Other
发起方
Theracos Inc
入组人数
300

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1.Male/female subjects >=18 years old
  • 2.Diagnosed with type 2 diabetes
  • 3.Body mass index(BMI)<= 45 Kg/m2
  • 4.HbA1c between 7 and 10%(Inclusive) as screening
  • 5.FPG <250 mg/dL at screening for subjects not treated with oral anti-diabetic therapies or FPG <240 mg/dL at screening for subjects treated with anti-diabetic therapies
  • 6.Diabetes currently treated with diet and exercise only or diet and exercise along with one approved oral anti-diabetic agent.
  • 7.If taking anti-diabetic medication, dose and regimen must be stable for past 3 months
  • 8.If taking anti-hypertensive medication, dose and regimen must be stable for past 3 months
  • 9.If taking lipid modifying therapy, dose and regimen must be stable for past 3 months
  • 10.Blood glucose level <250 mg/dL based on finger stick blood glucose for all subjects at randomization

排除标准

  • 1.Hemoglobinopathy that affects HbA1c measurement
  • 2.Current use of injected therapy for treatment of diabetes(insulin or GLP-1 receptor based therapy)
  • 3.Genitourinary tract infection within 6 weeks of screening
  • 4.Greater than 2 episodes of genitourinary tract infection in the past year
  • 5.History of kidney stones, bladder malfunctioning or other significant risk factor for urinary tract infections
  • 6.eGFR, as calculated by the modification of diet in renal disease study equation(MDRD), <50 mL/min/1.73 m2
  • 7.Abnormal tests of liver function ALT, AST or bilirubin >= 3x ULN
  • 8.Diagnosis of retinopathy or significant nephropathy (eGFR <50 mL/min/1.73 m2)
  • 9.Uncontrolled hypertension (systolic BP >160 or diastolic BP >95)
  • 10.Not willing to use effective birth control, if female with child bearing potential
  • 11.Life expectancy < 2 years
  • 12.New York Heart Association(NYHA) class 4 heart failure
  • 13.Sera positive of HCV, HIV, or positive on drug screen
  • 14.Currently participating in another interventional trial
  • 15.Previous treatment with EGT0001442 or EGT0001474
  • 16.Not able to comply with the study scheduled visits

研究者

发起方
Theracos Inc

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