LivingGLP1
Study S000752

Efficacy and Safety of LY2148568 in Japanese Patients With Type 2 Diabetes Who Are Treated With Oral Antidiabetic(s) But Not Well Controlled

Registration

Registration
NCT00577824
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
DOUBLE
Status
COMPLETED
Enrollment
181
Start
2008-01
Primary completion
2008-11
Lead sponsor
AstraZeneca
Conditions
Type 2 Diabetes
Interventions
DRUG:exenatide; DRUG:placebo
Results posted
TRUE

Registered primary outcomes

  • Change in Glycosylated Hemoglobin (HbA1c) From Baseline to Week 24 [baseline, 24 weeks]

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
R0018919Exenatide twice daily: analysis of effectiveness and safety data stratified by age, sex, race, duration of diabetes, and body mass index.
Pencek R, Postgraduate medicine
2012Randomized trialPMID 22913891DOIcites ClinicalTrials.gov:NCT00577824; registry reference DERIVED:22913891
R0018881Improved glycemic control and reduced bodyweight with exenatide: A double-blind, randomized, phase 3 study in Japanese patients with suboptimally controlled type 2 diabetes over 24 weeks.
Kadowaki T, Journal of diabetes investigation
2011Randomized trialPMID 24843486DOIcites ClinicalTrials.gov:NCT00577824; registry reference RESULT:24843486
R0026876Long-term safety and efficacy of exenatide twice daily in Japanese patients with suboptimally controlled type 2 diabetes.
Inagaki N, Journal of diabetes investigation
2011Randomized trialPMID 24843529DOIcites ClinicalTrials.gov:NCT00577824; registry reference RESULT:24843529