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Semaglutide and Cardiovascular Outcomes in Patients With Type 2 Diabetes
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Food and Drug Administration (FDA) and European Medicines Agency (EMA) approval in 2019 and 2020, respectively, for the second-line treatment of adults with insufficiently controlled T2D to improve glycaemic control as an adjunct to diet and exercise at the once-daily oral doses of 3, 7 and 14 mg [22, 23]
Because losing at least 5% of fasting body weight through lifestyle intervention during the 4- to 12-week run-in was a condition for their continued participation in the randomized treatment period, the results may not reflect those expected in the general population
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