LivingGLP1
Study S000232

Assessment of Dose-Dependent Effects of LY2189265 on Glycemic Control in Japanese Patients With Type 2 Diabetes

Registration

Registration
NCT01001104
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
TRIPLE
Status
COMPLETED
Enrollment
145
Start
2009-10
Primary completion
2010-12
Lead sponsor
Eli Lilly and Company
Conditions
Diabetes Mellitus, Type 2
Interventions
DRUG:LY2189265; DRUG:Placebo
Results posted
TRUE
Secondary identifiers
OTHER:H9X-JE-GBCZ

Registered primary outcomes

  • Change From Baseline in Glycosylated Hemoglobin (HbA1c) at 12 Weeks [Baseline, 12 weeks]

Linked records (0)

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