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Clinical Trial Details

Trial ID: L5323
Source ID: NCT01751399
Associated Drug: Ly2605541
Title: A Single Dose Study of LY2605541 in Participants With Liver Impairment
Acronym:
Status: COMPLETED
Study Results: YES
Results: https://ClinicalTrials.gov/show/NCT01751399/results
Conditions: Healthy Volunteers|Hepatic Insufficiency|Diabetes Mellitus, Type 2
Interventions: DRUG: LY2605541
Outcome Measures: Primary: Pharmacokinetics: Area Under the Concentration Time Curve From Zero to Infinity (AUC[0-∞]) of LY2605541, Predose and 2, 4, 6, 8, 12, 24, 36, 48, 72, 120, 168, and 216 hours postdose|Pharmacokinetics: Maximum Concentration (Cmax) of LY2605541, Predose and 2, 4, 6, 8, 12, 24, 36, 48, 72, 120, 168, and 216 hours postdose |
Sponsor/Collaborators: Sponsor: Eli Lilly and Company
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE1
Enrollment: 35
Study Type: INTERVENTIONAL
Study Designs: Allocation: NON_RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: TREATMENT
Start Date: 2012-12
Completion Date: 2013-09
Results First Posted: 2018-10-19
Last Update Posted: 2018-10-19
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., Munich, 81241, Germany|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., Balatonfured, 8230, Hungary
URL: https://clinicaltrials.gov/show/NCT01751399