LivingGLP1
Study S000246

A Phase 3 Study of LY2189265 Compared to Insulin Glargine in Patients With Type 2 Diabetes Mellitus on a Sulfonylurea and/or Biguanide

Registration

Registration
NCT01584232
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
NONE
Status
COMPLETED
Enrollment
361
Start
2012-04
Primary completion
2013-07
Lead sponsor
Eli Lilly and Company
Conditions
Type 2 Diabetes Mellitus
Interventions
DRUG:LY2189265; DRUG:Insulin glargine; DRUG:Sulfonylureas (SU); DRUG:Biguanide (BG)
Results posted
TRUE
Secondary identifiers
OTHER:H9X-JE-GBDY

Registered primary outcomes

  • Change From Baseline in Glycosylated Hemoglobin (HbA1c) at 26 Weeks [Baseline, 26 weeks]

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
R0021268The cost-effectiveness of dulaglutide versus insulin glargine for the treatment of type 2 diabetes mellitus in Japan.
Ishii H, Journal of medical economics
2018Other trialPMID 29357718DOIcites ClinicalTrials.gov:NCT01584232
R0021009Evaluation of the impact of once weekly dulaglutide on patient-reported outcomes in Japanese patients with type 2 diabetes: comparisons with liraglutide, insulin glargine, and placebo in two randomized studies.
Suzuki S, Health and quality of life outcomes
2017Randomized trialPMID 28606095DOIcites ClinicalTrials.gov:NCT01584232; registry reference DERIVED:28606095