Trial ID: | L6550 |
Source ID: | NCT01253278
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Associated Drug: |
Ly2393910
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Title: |
A Multiple-Ascending Dose Study in Type 2 Diabetes Mellitus Patients
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Acronym: |
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Status: |
COMPLETED
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Study Results: |
NO
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Results: |
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Conditions: |
Diabetes Mellitus, Type 2
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Interventions: |
DRUG: LY2393910|DRUG: Placebo
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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
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Sponsor/Collaborators: |
Sponsor: Eli Lilly and Company
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Gender: |
ALL
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Age: |
ADULT, OLDER_ADULT
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Phases: |
PHASE1
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Enrollment: |
38
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Study Type: |
INTERVENTIONAL
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Study Designs: |
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: DOUBLE (PARTICIPANT, INVESTIGATOR)|Primary Purpose:
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Start Date: |
2010-03
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Completion Date: |
2011-05
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Results First Posted: |
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Last Update Posted: |
2011-06-10
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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
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URL: |
https://clinicaltrials.gov/show/NCT01253278
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