LivingGLP1
Study S001852

A Randomized Trial Comparing Insulin Lispro Protamine Suspension With Insulin Glargine in Subjects With Type 2 Diabetes on Oral Antihyperglycemic Medications and Exenatide

Registration

Registration
NCT00560417
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
NONE
Status
COMPLETED
Enrollment
339
Start
2007-11
Primary completion
2009-12
Lead sponsor
Eli Lilly and Company
Conditions
Diabetes Mellitus, Type 2
Interventions
DRUG:Insulin Lispro Protamine Suspension; DRUG:Insulin Glargine
Results posted
TRUE
Secondary identifiers
OTHER:F3Z-US-IOPB

Registered primary outcomes

  • Change From Baseline in Hemoglobin A1C (HbA1c) at Endpoint (Last Observation Carried Forward [LOCF]) [Baseline, Endpoint (LOCF) up to 24 weeks]

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