LivingGLP1
Study S000320

Safety and Efficacy of Exenatide as Monotherapy in Drug Naive Patients With Type 2 Diabetes

Registration

Registration
NCT00381342
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
DOUBLE
Status
COMPLETED
Enrollment
233
Start
2006-09
Primary completion
2007-09
Lead sponsor
AstraZeneca
Conditions
Type 2 Diabetes Mellitus
Interventions
DRUG:exenatide; DRUG:placebo
Results posted
FALSE

Registered primary outcomes

  • Change in HbA1c (glycosylated hemoglobin) from Baseline to Week 24 [Baseline, Week 24]

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:NCT00381342; registry reference DERIVED:22913891
R0026474Clinical relevance of anti-exenatide antibodies: safety, efficacy and cross-reactivity with long-term treatment.
Fineman MS, Diabetes, obesity & metabolism
2012OtherPMID 22236356DOIcites ClinicalTrials.gov:NCT00381342; registry reference DERIVED:22236356
R0027392Efficacy and tolerability of exenatide monotherapy over 24 weeks in antidiabetic drug-naive patients with type 2 diabetes: a randomized, double-blind, placebo-controlled, parallel-group study.
Moretto TJ, Clinical therapeutics
2008Randomized trialPMID 18803987DOIregistry reference RESULT:18803987