Study identifier:BCB120
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Randomized, Long-Term, Open-Label, 3-Arm, Multicenter Study to Compare the Glycemic Effects, Safety, and Tolerability of Exenatide Once Weekly Suspension to Sitagliptin and Placebo in Subjects With Type 2 Diabetes Mellitus
Diabetes Type 2
Phase 3
No
Exenatide once weekly suspension, Sitagliptin, Placebo
All
365
Interventional
18 Years +
Allocation: Randomized
Endpoint Classification: Safety/Efficacy
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Verified 01 Jun 2015 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
-
To compare the effect on glycemic control (HbA1c) of exenatide suspension administered once weekly to that achieved by sitagliptin or placebo administered once daily for 28 weeks in subjects with type 2 diabetes mellitus.
Location
Location
Omaha, NE, United States, 68130
Location
Rapid City, SD, United States, 57702
Location
Hialeah, FL, United States, 33012
Location
Miami, FL, United States, 33183
Location
Albuquerque, NM, United States, 87102
Location
Eugene, OR, United States, 97404
Location
Walnut Creek, CA, United States, 94598
Location
Burke, VA, United States, 22015
Arms | Assigned Interventions |
---|---|
Experimental: Exenatide once weekly suspension Exenatide once weekly suspension 2mg subcutaneous injection | - |
Active Comparator: Sitagliptin 100mg Overencapsulated Sitagliptin 100mg oral tablet once daily | - |
Placebo Comparator: Placebo Placebo oral capsule once daily | Drug: Placebo Placebo oral capsule once daily |
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