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Clinical Trial Details

Trial ID: L6550
Source ID: NCT01253278
Associated Drug: Ly2393910
Title: A Multiple-Ascending Dose Study in Type 2 Diabetes Mellitus Patients
Acronym:
Status: COMPLETED
Study Results: NO
Results:
Conditions: Diabetes Mellitus, Type 2
Interventions: DRUG: LY2393910|DRUG: Placebo
Outcome Measures: Primary: Number of Participants with Clinically Significant Effects, Over four weeks | Secondary: Pharmacokinetics of LY2393910, Area Under the Curve (AUC), From predose Day 1 up until Day 19|Change from baseline to day 28 in glucagon, Baseline, day 28|Pharmacokinetics of LY2393910, maximum concentration (Cmax), From predose Day 1 up until Day 19|Change from baseline to day 28 in glucose-like peptide 1 (GLP-1), Baseline, day 28|Change from baseline to day 14 in insulin, baseline, day 14|Change from baseline to day 14 in proinsulin, baseline, day 14|Change from baseline to day 28 in glucose, baseline, day 28|Change from baseline to day 14 in C-peptide, baseline, day 14
Sponsor/Collaborators: Sponsor: Eli Lilly and Company
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE1
Enrollment: 38
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: DOUBLE (PARTICIPANT, INVESTIGATOR)|Primary Purpose:
Start Date: 2010-03
Completion Date: 2011-05
Results First Posted:
Last Update Posted: 2011-06-10
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., Neuss, D-41460, Germany
URL: https://clinicaltrials.gov/show/NCT01253278