LivingGLP1
Study S000536

Multiple-Dose Study to Examine Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of LY2148568 Long-Acting Release in Japanese Patients With Type 2 Diabetes Mellitus

Registration

Registration
NCT00612794
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
30
Start
2007-09
Primary completion
2008-05
Lead sponsor
AstraZeneca
Conditions
Type 2 Diabetes
Interventions
DRUG:exenatide once weekly; DRUG:placebo
Results posted
FALSE

Registered primary outcomes

  • To assess the safety and tolerability of exenatide administered once weekly by subcutaneous (SC) injection in subjects with type 2 diabetes mellitus. [10 weeks]

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
R0027116Safety, tolerability, pharmacokinetics, and pharmacodynamics of exenatide once weekly in Japanese patients with type 2 diabetes.
Iwamoto K, Endocrine journal
2009Randomized trialPMID 19706990DOIcites ClinicalTrials.gov:NCT00612794; registry reference DERIVED:19706990