Efficacy and Safety of FIAsp Compared to Insulin Aspart in Combination With Insulin Glargine and Metformin in Adults With Type 2 Diabetes
Status: | Completed |
---|---|
Conditions: | Diabetes, Diabetes |
Therapuetic Areas: | Endocrinology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 2/1/2019 |
Start Date: | September 9, 2013 |
End Date: | January 22, 2015 |
This trial is conducted in Asia, Europe and North America. The aim of the trial is to compare
FIAsp (faster-acting insulin aspart) to insulin aspart, both in combination with insulin
glargine and metformin in adults with type 2 diabetes.
FIAsp (faster-acting insulin aspart) to insulin aspart, both in combination with insulin
glargine and metformin in adults with type 2 diabetes.
Inclusion Criteria: - Type 2 diabetes (diagnosed clinically) for 6 months or longer at time
of screening (visit 1) - Treated with basal insulin for at least 6 months prior to
screening (visit 1) - Current once daily treatment with insulin NPH (Neutral Protamine
Hagedorn), insulin detemir or glargine for at least 3 months prior to the screening visit
(visit 1) - Current treatment with: a. metformin with unchanged dosing for at least 3
months prior to screening (visit 1). The metformin dose must be at least 1000 mg or b.
metformin in combination with sulfonylurea (SU) or glinide or DPP-IV (dipeptidyl
peptidase-4) inhibitors and/or alpha-glucosidase inhibitors (AGI) with unchanged dosing for
at least 3 months prior to screening (visit 1). The metformin dose must be at least 1000 mg
- HbA1c by central laboratory: a. 7.0 - 9.5% (53 - 80 mmol/mol) (both inclusive) in the
metformin group at the screening visit (visit 1) or b. 7.0 - 9.0% (53 - 75 mmol/mol) (both
inclusive) in the metformin + other OAD (oral antidiabetic drug) (SU, glinide, DDP-IV
inhibitors, AGI) combination group at the screening visit (visit 1) - Body mass index (BMI)
equal to or below 40.0 kg/m^2 Exclusion Criteria: - Any use of bolus insulin, except
short-term use due to intermittent illness (no longer than 14 days consecutive treatment)
and not 3 months prior to the screening visit (visit 1) - Use of GLP-1 (glucagon-like
peptide-1) agonists and/or TZDs within the last 3 months prior to screening (visit 1) -
Recurrent severe hypoglycaemia (more than 1 severe hypoglycaemic event during the last 12
months) or hypoglycaemic unawareness as judged by the Investigator or hospitalisation for
diabetic ketoacidosis during the previous 6 months prior to screening (visit 1) -
Cardiovascular disease, within the last 6 months prior to screening (visit 1), defined as:
stroke, decompensated heart failure New York Heart Association (NYHA) class III or IV,
myocardial infarction, unstable angina pectoris or coronary arterial bypass graft or
angioplasty
We found this trial at
72
sites
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