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Clinical Trial Details

Trial ID: L3385
Source ID: NCT01588366
Associated Drug: Placebo
Title: The Effects of LY2409021 on the Liver
Acronym:
Status: COMPLETED
Study Results: YES
Results: https://ClinicalTrials.gov/show/NCT01588366/results
Conditions: Diabetes Mellitus, Type 2
Interventions: DRUG: Placebo|DRUG: LY2409021
Outcome Measures: Primary: Change From Baseline to Day 28 in Liver Fat Average Percent (%), Measured by magnetic resonance (MR) scanning., Baseline, Day 28 (Pre-meal)|Change From Baseline to Day 28 in Hepatic Glycogen Content, Measured by MR scanning., Baseline, Day 28 (Pre-meal) | Secondary: Change From Baseline to Day 28 in Transaminase Levels, Baseline, Day 28|Change From Baseline to Day 29 in Glucose Response to an Arginine Stimulation Test (AST) (Part A), Acute glucose response to an AST at a blood glucose level of approximately 250 milligrams per deciliter (mg/dL)., Baseline, Day 29|Change From Baseline to Day 29 in Glucagon Response to an Arginine Stimulation Test (AST) (Part A), Acute glucagon response to an AST at a blood glucose level of approximately 250 mg/dL., Baseline, Day 29|Change From Baseline to Day 29 in Insulin Response to an Arginine Stimulation Test (AST) (Part A), Acute insulin response to an AST at a blood glucose level of approximately 250 mg/dL., Baseline, Day 29
Sponsor/Collaborators: Sponsor: Eli Lilly and Company
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE1
Enrollment: 30
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: SINGLE (PARTICIPANT)|Primary Purpose: BASIC_SCIENCE
Start Date: 2012-04
Completion Date: 2013-09
Results First Posted: 2019-03-07
Last Update Posted: 2019-03-07
Locations: For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST) or speak with your personal physician., Singapore, Singapore
URL: https://clinicaltrials.gov/show/NCT01588366