LivingGLP1
Study S001267

A Phase 2, Randomized, Triple-Blind, Placebo-Controlled, Multicenter Study to Examine the Effect of Exenatide Monotherapy on Glucose Control in Subjects With Type 2 Diabetes Mellitus

Registration

Registration
NCT00085969
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
DOUBLE
Status
COMPLETED
Enrollment
99
Start
2003-09
Primary completion
2004-01
Lead sponsor
AstraZeneca
Conditions
Diabetes Mellitus, Type 2
Interventions
DRUG:Placebo 0.04 mL twice daily; DRUG:Placebo 0.04 mL once daily; DRUG:Placebo 0.08 mL once daily; DRUG:B - Exenatide 10 mcg twice daily; DRUG:C - Exenatide 10 mcg once daily; DRUG:Exenatide 20 mcg once daily
Results posted
FALSE

Registered primary outcomes

  • Change in HbA1c (glycosylated hemoglobin) from Baseline to Day 28 [Baseline, Day 28]

Linked records (1)

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
R0025690The incretin mimetic exenatide as a monotherapy in patients with type 2 diabetes.
Nelson P, Diabetes technology & therapeutics
2007Randomized trialPMID 17705687DOIcites ClinicalTrials.gov:NCT00085969; registry reference DERIVED:17705687