Effect of Liraglutide or Exenatide Added to an Ongoing Treatment on Blood Glucose Control in Subjects With Type 2 Diabetes
Part of paid clinical trials in Birmingham, Alabama.
- Sponsor
- Novo Nordisk A/S
- Study ID
- NCT00518882
- 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 — DRUG1.8 mg once daily for s.c. (under the skin) injection.
- exenatide — DRUG10 mcg twice daily for s.c. (under the skin) injection.
Study Details
This trial is conducted in Europe and the United States of America (USA). The aim of this trial is to compare the effect on glycaemic control of liraglutide or exenatide when added to subject's ongoing OAD (oral anti-diabetic drug) treatment of either metformin, sulphonylurea or a combination of both in subjects with type 2 diabetes. Two trial periods: A 26 week randomised, followed by a 52 week extension (14 + 38 weeks) where all subjects received liraglutide + OAD after previous randomisation to either liraglutide or exenatide, both combined with OAD treatment.
Key Dates
- Start date
- Aug 31, 2007
- Status verified
- Jan 2017
- Primary completion
- Apr 30, 2008
- Completion
- Apr 30, 2009
Study Design
- Enrollment
- 467 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: LiraglutideLiraglutide 1.8 mg once daily + subject's own OAD treatment
- Active Comparator: ExenatideExenatide 10 mcg twice daily + subject's own OAD treatment
Primary Outcome Measure
Change in Glycosylated A1c (HbA1c) at Week 26 [ Time Frame: week 0, week 26 ]
Locations (61)
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