Study to Evaluate the Effect of BYDUREON on 24-hour Glucose Control in Metformin Treated Patients With Type 2 Diabetes.
Completed · Phase 4 · Has a placebo group
Conditions studied: Type 2 Diabetes
In brief
A Randomized, Double-blind, Parallel-group Study to Evaluate the Effect of Bydureon Compared with Placebo on 24-hour Glucose Control in Metformin-treated Patients with Type 2 Diabetes.
Key facts
- Study ID
- NCT02288273
- Run by
- AstraZeneca
- People needed
- 239
- Starts
- 2014-12-01
- Expected to finish
- 2015-08-01
- Last updated by the study team
- 2017-01-27
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Type 2 diabetes mellitus (T2DM) treated with stable dose of metformin > or = to 1500mg/day as monotherapy for at least 8 weeks
- Hemoglobin A1c (HbA1c) 7% to 10% at screening
- Body mass index (BMI) < or = to 45 kg/m2
You may not qualify if…
- History of taking antihyperglycemic therapy other than metformin or metformin extended release (XR) during the 8 weeks prior to screening
- History of taking a dipeptidyl peptidase-4 (DPP-4) inhibitor or pramlintide during 12 weeks prior to screening
- History of potent, inhaled or intrapulmonary steroids 3 months prior to screening or during the study
- History of prescription or over the counter weight loss medication during 3 months prior to screening
- Previous exposure to exenatide or any glucagon-like peptide-1 (GLP-1) receptor agonist during 6 months prior to screening
Where it is running
- Research Site — Anaheim, California, United States
- Research Site — Chino, California, United States
- Research Site — Los Angeles, California, United States
- Research Site — North Hollywood, California, United States
- Research Site — Santa Ana, California, United States
- Research Site — Spring Valley, California, United States
- Research Site — Tustin, California, United States
- Research Site — Walnut Creek, California, United States
- Research Site — Hollywood, Florida, United States
- Research Site — Miami, Florida, United States
- Research Site — Port Orange, Florida, United States
- Research Site — Marietta, Georgia, United States
- Research Site — Chicago, Illinois, United States
- Research Site — Edina, Minnesota, United States
- Research Site — St Louis, Missouri, United States
- Research Site — Butte, Montana, United States
- Research Site — Las Vegas, Nevada, United States
- Research Site — Franklin, Ohio, United States
- Research Site — Marion, Ohio, United States
- Research Site — Oklahoma City, Oklahoma, United States
- Research Site — Mt. Pleasant, South Carolina, United States
- Research Site — Rapid City, South Dakota, United States
- Research Site — Corpus Christi, Texas, United States
- Research Site — Houston, Texas, United States
- Research Site — Katy, Texas, United States
Full record on ClinicalTrials.gov
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