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.
Peking University First Hospital, Beijing, Beijing, China
Peking University People's Hospital, Beijing, Beijing, China
Michael E. DeBakey VA Medical Center, Houston, Texas, United States
Peking University Third Hospital drug clinical trial Institute, Beijing, Beijing, China
Amish Research Clinic, Lancaster, Pennsylvania, United States
CMax, Adelaide, Australia
Research Site, London, United Kingdom
Michael E. DeBakey VA Medical Center, Houston, Texas, United States
The University of Texas Health Science Center at Houston, Houston, Texas, United States
Magee Womens Hospital of UPMC, Pittsburgh, Pennsylvania, United States
Chinese University of Hong Kong, Hong Kong, Hong Kong
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