The Effect of Liraglutide Versus Placebo When Added to Basal Insulin Analogues With or Without Metformin in Subjects With Type 2 Diabetes
Part of paid clinical trials in Phoenix, Arizona.
- Sponsor
- Novo Nordisk A/S
- Study ID
- NCT01617434
- Phase
- PHASE3
- Status
- Completed
Conditions
- Diabetes
- Diabetes Mellitus, Type 2
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 80 Years
- Healthy Volunteers
- Not accepted
Interventions
- liraglutide — DRUGMaximum 1.8 mg administered s.c. (subcutaneously, under the skin) once daily in addition to the subject's stable pre-trial basal insulin analogue regimen plus/minus metformin.
- placebo — DRUGPlacebo administered s.c. (subcutaneously, under the skin) once daily in addition to the subject's stable pre-trial basal insulin analogue regimen plus/minus metformin.
Study Details
This trial is conducted in Asia, Europe and North and South America. The aim of the trial is to investigate the effect of liraglutide versus placebo when added to basal insulin analogues with or without metformin in subjects with type 2 diabetes.
Key Dates
- Start date
- Sep 30, 2012
- Status verified
- Jan 2017
- Primary completion
- Oct 31, 2013
- Completion
- Oct 31, 2013
Study Design
- Enrollment
- 451 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Liraglutide
- Placebo Comparator: Placebo
Primary Outcome Measure
Change in Glycosylated Haemoglobin (HbA1c) From Baseline to Week 26 [ Time Frame: Week 0 to Week 26 ]
Locations (31)
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