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Clinical Trial Details

Trial ID: L2599
Source ID: NCT05762744
Associated Drug: Exenatide Injection
Title: Pharmacogenomics of GLP1 Receptor Agonists
Acronym:
Status: TERMINATED
Study Results: NO
Results:
Conditions: Type 2 Diabetes
Interventions: DRUG: Exenatide Injection|DRUG: Saline injection
Outcome Measures: Primary: First phase insulin secretion (placebo), The area under the curve for plasma insulin levels during a frequently sampled intravenous glucose tolerance test after participants received saline, 0-10 minutes|First phase insulin secretion (exenatide), The area under the curve for plasma insulin levels during a frequently sampled intravenous glucose tolerance test after participants received exenatide, 0-10 minutes|Exenatide effect on first phase insulin secretion, The difference between the logarithm of first phase insulin secretion (exenatide) minus the logarithm of the first phase insulin secretion (placebo), 0-10 minutes|glucose disappearance rate (placebo), The slope of the line plotting the logarithm of glucose concentrations as a function of time during the placebo frequently sampled intravenous glucose tolerance test, 25-50 minutes|glucose disappearance rate (exenatide), The slope of the line plotting the logarithm of glucose concentrations as a function of time during the exenatide frequently sampled intravenous glucose tolerance test, 25-50 minutes|Exenatide effect on glucose disappearance rate, The difference between glucose disappearance rate (exenatide) minus glucose disappearance rate (placebo), 25-50 minutes |
Sponsor/Collaborators: Sponsor: University of Maryland, Baltimore
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE1
Enrollment: 78
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: CROSSOVER|Masking: SINGLE (PARTICIPANT)|Primary Purpose: BASIC_SCIENCE
Start Date: 2016-06-01
Completion Date: 2022-10-31
Results First Posted:
Last Update Posted: 2023-03-10
Locations: Amish Research Clinic, Lancaster, Pennsylvania, 17602, United States
URL: https://clinicaltrials.gov/show/NCT05762744