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Adverse events: There were no unexpected safety findings, however, gastrointestinal (GI) side effects were a main cause of treatment discontinuation, which occurred in 16.6% of patients in the semaglutide group vs

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The OASIS 3 trial assessed the therapeutic efficacy and clinical safety profile of once-daily oral semaglutide50 mgversus placebo in 200 Chinese adults who were obese and overweight with one or more weight-related comorbidities, including T2DM