LivingGLP1
Study S000697

A 52-Week, Open-Label, Long-Term Safety Study of LY2189265 in Combination With Monotherapy of Oral Antihyperglycemic Medications in Patients With Type 2 Diabetes Mellitus

Registration

Registration
NCT01468181
Study type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Phase
PHASE3
Masking
NONE
Status
COMPLETED
Enrollment
394
Start
2011-11
Primary completion
2013-12
Lead sponsor
Eli Lilly and Company
Conditions
Type 2 Diabetes Mellitus
Interventions
DRUG:LY2189265; DRUG:Sulfonylureas (SU); DRUG:Biguanides (BG); DRUG:alpha-glucosidase inhibitor (a-GI); DRUG:Thiazolidinedione (TZD); DRUG:Glinides
Results posted
TRUE
Secondary identifiers
OTHER:H9X-JE-GBDQ

Registered primary outcomes

  • Percentage of Participants With Treatment-Emergent Adverse Events (TEAEs) [Baseline through 52 Weeks]
  • Percentage of Participants With Hypoglycemic Episodes [Baseline through 52 Weeks]

Linked records (0)

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