Can Exenatide Prevent Increase in EGP in Response to Dapagliflozin-induced Increase in Glucosuria
NCT03331289 · Completed
Last updated 2026-05-28This clinical trial is testing whether the drug exenatide can prevent an increase in blood sugar production in adults with type 2 diabetes when another drug, dapagliflozin, causes more sugar to be lost in the urine.
What this study is testing ClinicalTrials.gov NCT03331289 ↗
Description as written by the study sponsor.
Research Design/Plan: After screening, each subject will receive 1 measurements of Endogenous Glucose Production \[EGP\] with prime-continuous Infusion of 3-3H-glucose. After completing the EGP measurement each subject will receive a Double Tracer Oral Glucose Tolerance Test \[OGTT\]. Methods: Visit 1: Screening. Medical history will be obtained, physical exam performed, and pregnancy test performed. Visit 2: Endogenous Glucose Production Measurement: The rate of EGP will be measured with 3-3H-glucose. Visit 3: Double Tracer OGTT
Treatments tested
- Placebo also known as Placebo drug Drug
Placebo will be administered to 20 subjects after a 3 hour tracer equilibration period
- Exenatide also known as Byetta, Bydureon Drug
Exenatide will be administered to 20 subjects after a 3 hour tracer equilibration period
- Dapagliflozin also known as Farxiga Drug
Dapagliflozin will be administered to 20 subjects after a 3 hour tracer equilibration period
- Exenatide and Dapagliflozin also known as Byetta plus Dapagliflozin Drug
Exenatide and Dapagliflozin will be administered to 20 subjects after a 3 hour tracer equilibration period
| Main thing measured | Change in EGP From Baseline to Post-oral Glucose Load. |
|---|---|
| Sponsor | The University of Texas Health Science Center at San Antonio |
| Conditions studied | Diabetes Mellitus, Type 2 |
| GLP-1 drugs | exenatide |
Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT03331289 ↗