Exenatide is a glucagon-like peptide-1 (GLP-1) analog. It activates the GLP-1 receptor and increases insulin secretion, decreases glucagon secretion, and slows gastric emptying to improve glycemic control. Exenatide was given FDA approval on April 28, 2005. It is available as immediate- and extended-release formulations. Bydureon, the brand name product of extended-release exenatide in an injectable suspension, was discontinued in 2021. Bydureon BCise, an auto-injector extended-release formulation, remains available.
Exenatide is indicated as an adjunct to diet and exercise to improve glycemic control in patients with type 2 diabetes. An extended-release formulation is available which is indicated in patients ≥10 years old, while the immediate-acting formulation is approved only for adult patients.
Renji Hospital Department of Endocrinology and Metabolism, Shanghai, Shanghai, China
Amsterdam UMC, location VU Medical Center, Amsterdam, Noord-Holland, Netherlands
Renji Hospital Department of Endocrinology and Metabolism, Shanghai, China
University Health System Texas Diabetic Institute, San Antonio, Texas, United States
Austin Hospital, Heidelberg, Victoria, Australia
Royal Melbourne Hospital, Parkville, Victoria, Australia
Helsinki University Hospital, Helsinki, Finland
Novavì ambulatorierne, Copenhagen, Frederiksberg, Denmark
Clinical Research Site, Evansville, Indiana, United States
Tartu University Hospital, Tartu, Estonia
Diabetes Endocrinology Research Center of WNY, Williamsville, New York, United States
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