Safety and Efficacy of Liraglutide in Combination With an OAD in Subjects With Type 2 Diabetes Insufficiently Controlled on OAD Alone
- Sponsor
- Novo Nordisk A/S
- Study ID
- NCT01512108
- Phase
- PHASE3
- Status
- Completed
Conditions
- Diabetes
- Diabetes Mellitus, Type 2
Eligibility Criteria
- Sex
- ALL
- Age
- 20 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- liraglutide — DRUG0.9 mg/day liraglutide was injected once daily subcutaneously (s.c., under the skin).
- oral anti-diabetic drug — DRUGAn additional oral anti-diabetic drug (OAD) with a different mechanism of action than the pre-trial OAD. The type and dosage of the additional OAD should be chosen by the investigator within the Japanese labelled dose.
Study Details
This trial was conducted in Japan. The aim of this trial was to evaluate the safety and efficacy of once daily administration of liraglutide in combination with an oral anti-diabetic drug (OAD) in Japanese subjects with type 2 diabetes who are insufficiently controlled on OAD monotherapy. All subjects will continue their pre-trial OAD (either glinide, metformin, alpha-glucosidase inhibitor or thiazolidinedione) during the trial at unchanged type and dose.
Key Dates
- Start date
- Jan 10, 2012
- Status verified
- Nov 2017
- Primary completion
- Apr 26, 2013
- Completion
- Apr 26, 2013
Study Design
- Enrollment
- 363 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Liraglutide + an OAD therapy
- Active Comparator: Two OADs combination therapy
Primary Outcome Measure
Incidence of Treatment Emergent Adverse Events (AEs) [ Time Frame: Week 0 to Week 52 + 7 days ]
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