LivingGLP1
Study S001305

Safety and Efficacy of Exenatide in Patients With Type 2 Diabetes Using Thiazolidinediones or Thiazolidinediones and Metformin

Registration

Registration
NCT00099320
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
DOUBLE
Status
COMPLETED
Enrollment
182
Start
2004-05
Primary completion
2005-08
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 16, and if measured, any visits in between [Baseline, Week 4, Week 8, Week 12, Week 16]
  • Change from Baseline to Week 16 in fasting serum glucose (FSG) and glucose [Baseline, Week 16]

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
R0026474Clinical relevance of anti-exenatide antibodies: safety, efficacy and cross-reactivity with long-term treatment.
Fineman MS, Diabetes, obesity & metabolism
2012OtherPMID 22236356DOIcites ClinicalTrials.gov:NCT00099320; registry reference DERIVED:22236356
R0027482The effect of adding exenatide to a thiazolidinedione in suboptimally controlled type 2 diabetes: a randomized trial.
Zinman B, Annals of internal medicine
2007Randomized trialPMID 17404349DOIcites ClinicalTrials.gov:NCT00099320; registry reference DERIVED:17404349