Efficacy and Safety of Empagliflozin (BI 10773) With Metformin in Patients With Type 2 Diabetes
Status: | Completed |
---|---|
Conditions: | Diabetes |
Therapuetic Areas: | Endocrinology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/21/2016 |
Start Date: | August 2010 |
End Date: | August 2015 |
A Phase III Randomised, Double-blind, Active-controlled Parallel Group Efficacy and Safety Study of BI 10773 Compared to Glimepiride Administered Orally During 104 Weeks With a 104 Week Extension Period in Patients With Type 2 Diabetes Mellitus and Insufficient Glycaemic Control Despite Metformin Treatment
This is a pivotal phase III study, mandatory to seek approval by regulatory authorities for
BI 10773 as an anti-diabetic agent compared to an active comparator in patients with type 2
diabetes mellitus and insufficient glycaemic control.
BI 10773 as an anti-diabetic agent compared to an active comparator in patients with type 2
diabetes mellitus and insufficient glycaemic control.
Inclusion criteria:
- Diagnosis typ 2 diabetes mellitus
- Male and female on diet and exercise regimen, pre-treated with metformin 12 weeks
prior to randomisation
- HbA1c equal or greater than 7.0% and less than or equal to 10% at visit 1
- 18 years or more
- BMI equal or less than 45Kg/m2
Exclusion criteria:
- Uncontrolled hyperglycemia defined as glucose more that 13.3 mmol/L after overnight
fast during placebo run-in
- Any other antidiabetic drug within 12 weeks prior to randomisation except metformin
- Acute coronary syndrome (non-STEMI, STEMI unstable angina pectoris), stroke or
transient ischemic attack within 12 weeks of informed consent
- Indication of liver disease
- Moderate to severe renal impairment
- Bariatric surgery within past 2 years
- Medical history of cancer or treatment for cancer within last 5 years
- Blood dyscrasias or any disorders causing haemolysis or unstable red blood cell
- Contraindications hypersensitivity to concomitant drugs
- Treatment with anti-obesity drugs
We found this trial at
24
sites
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