LivingGLP1
Study S000337

The Effect of Dose Titration of LY2189265 in Overweight and Obese Patients With Type 2 Diabetes Mellitus

Registration

Registration
NCT00630825
Acronym
EGO
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
TRIPLE
Status
COMPLETED
Enrollment
262
Start
2008-04
Primary completion
2009-01
Lead sponsor
Eli Lilly and Company
Conditions
Diabetes Mellitus Type 2
Interventions
DRUG:LY2189265; DRUG:Placebo
Results posted
TRUE
Secondary identifiers
OTHER:H9X-MC-GBCJ

Registered primary outcomes

  • Change From Baseline in Glycosylated Hemoglobin (HbA1c) in Overweight and Obese Participants With Type 2 Diabetes Mellitus [Baseline, 16 weeks]

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