LivingGLP1
Study S001212

The Effect of LY2189265 on Insulin Secretion in Response to Intravenous Glucose Infusion

Registration

Registration
NCT01300260
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
TRIPLE
Status
COMPLETED
Enrollment
32
Start
2011-02
Primary completion
2011-08
Lead sponsor
Eli Lilly and Company
Conditions
Diabetes Mellitus, Type 2
Interventions
BIOLOGICAL:LY2189265; DRUG:Placebo; DRUG:Insulin; DRUG:Glucose; DRUG:Glucagon
Results posted
TRUE
Secondary identifiers
OTHER:H9X-MC-GBCI

Registered primary outcomes

  • Maximum Insulin Concentration (Cmax) - First Phase Response [0-10 minutes after dextrose bolus on Day 3 postdose]
  • Area Under the Insulin Concentration-time Curve (AUC) - First Phase Response [0-10 minutes after dextrose bolus on Day 3 postdose]
  • Maximum Insulin Concentration (Cmax) - Second Phase Response [10-180 minutes after dextrose bolus on Day 3 postdose]
  • Insulin Area Under the Curve (AUC) - Second Phase Response [10-180 minutes after dextrose bolus on Day 3 post dose]

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