LivingGLP1
Study S000233

A 52-week, Multi-centre, Open-labelled, Randomised (2:1), Parallel-group Trial With an Active Control (Two OADs Combination Therapy) to Evaluate the Safety and Efficacy of Liraglutide in Combination With an OAD in Subjects With Type 2 Diabetes Insufficiently Controlled on OAD Monotherapy

Registration

Registration
NCT01512108
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
NONE
Status
COMPLETED
Enrollment
363
Start
2012-01-10
Primary completion
2013-04-26
Lead sponsor
Novo Nordisk A/S
Conditions
Diabetes; Diabetes Mellitus, Type 2
Interventions
DRUG:liraglutide; DRUG:oral anti-diabetic drug
Results posted
TRUE
Secondary identifiers
OTHER:U1111-1121-3457; REGISTRY:JapicCTI-121744

Registered primary outcomes

  • Incidence of Treatment Emergent Adverse Events (AEs) [Week 0 to Week 52 + 7 days]

Linked records (2)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R0011989Safety and efficacy of the combination of the glucagon-like peptide-1 receptor agonist liraglutide with an oral antidiabetic drug in Japanese patients with type 2 diabetes: Post-hoc analysis of a randomized, 52-week, open-label, parallel-group trial.
Kiyosue A, Journal of diabetes investigation
2018Randomized trialPMID 28984041DOIregistry reference RESULT:28984041
R0026134Liraglutide is effective and well tolerated in combination with an oral antidiabetic drug in Japanese patients with type 2 diabetes: A randomized, 52-week, open-label, parallel-group trial.
Kaku K, Journal of diabetes investigation
2016Randomized trialPMID 26816604DOIcites ClinicalTrials.gov:NCT01512108; registry reference RESULT:26816604