A Trial Comparing the Efficacy and Safety of Insulin Degludec/Liraglutide and Insulin Degludec in Subjects With Type 2 Diabetes
Part of paid clinical trials in Huntsville, Alabama.
- Sponsor
- Novo Nordisk A/S
- Study ID
- NCT01392573
- Phase
- PHASE3
- Status
- Completed
Conditions
- Diabetes
- Diabetes Mellitus, Type 2
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- insulin degludec/liraglutide — DRUGIDeg/Lira treatment will be initiated and titrated (individually adjusted) twice weekly according to the mean self measured plasma glucose (SMPG) (fasting). IDegLira is injected subcutaneously (under the skin) once daily.
- insulin degludec — DRUGIDeg treatment will be initiated and titrated (individually adjusted) twice weekly according to the mean self measured plasma glucose (SMPG) (fasting). IDeg is injected subcutaneously (under the skin) once daily.
Study Details
This trial is conducted in Asia, Europe and the United States of America (USA). The aim of this trial is to compare the efficacy and safety of insulin degludec/liraglutide (IDegLira) and insulin degludec (IDeg) in subjects with type 2 diabetes. Subjects continue their pre-trial treatment with metformin throughout the entire trial.
Key Dates
- Start date
- Nov 28, 2011
- Status verified
- Dec 2018
- Primary completion
- Oct 1, 2012
- Completion
- Oct 4, 2012
Study Design
- Enrollment
- 413 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: IDegLira + metforminIDegLira was injected subcutaneously once daily for 26 weeks.
- Experimental: IDeg + metforminIDeg was injected subcutaneously once daily for 26 weeks.
Primary Outcome Measure
Change From Baseline in HbA1c (Glycosylated Haemoglobin) [ Time Frame: Week 0, week 26 ]
Locations (58)
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