LivingGLP1
Study S000703

A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel Group, Phase 3 Trial to Evaluate the Safety and Efficacy of Once Weekly Exenatide Therapy Added to Titrated Basal Insulin Glargine Compared to Placebo Added to Titrated Basal Insulin Glargine in Patients With Type 2 Diabetes Who Have Inadequate Glycemic Control on Basal Insulin Glargine With or Without Metformin

Registration

Registration
NCT02229383
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
DOUBLE
Status
COMPLETED
Enrollment
464
Start
2014-09-06
Primary completion
2016-08-29
Lead sponsor
AstraZeneca
Conditions
Diabetes Mellitus
Interventions
DRUG:Exenatide; DRUG:Exenatide matching placebo
Results posted
TRUE
Secondary identifiers
EUDRACT_NUMBER:2014-003502-33; NIH:2014

Registered primary outcomes

  • Change in HbA1c From Baseline to Week 28 [Baseline to Week 28]

Linked records (3)

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
R0013562Safety and Efficacy of Exenatide Once Weekly in Participants with Type 2 Diabetes and Stage 2/3 Chronic Kidney Disease.
Guja C, Diabetes therapy : research, treatment and education of diabetes and related disorders
2020Other trialPMID 32306296DOIcites ClinicalTrials.gov:NCT02229383; registry reference DERIVED:32306296
R0014763Effect of exenatide QW or placebo, both added to titrated insulin glargine, in uncontrolled type 2 diabetes: The DURATION-7 randomized study.
Guja C, Diabetes, obesity & metabolism
2018Randomized trialPMID 29473704DOIcites ClinicalTrials.gov:NCT02229383; registry reference DERIVED:29473704
R0053153Wirksamkeit und Verträglichkeit von Depot-Exenatide gegenüber Placebo als Add-on zu Insulin glargin bei Typ-2-Diabetes-Patienten mit unzureichender glykämischer Kontrolle unter Basalinsulin: Duration-7-Studie
JP Frias, Diabetologie und Stoffwechsel
2018OtherDOIcites ClinicalTrials.gov:NCT02229383