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Full analysis set: all randomised participants who were exposed to at least one dose of study product and completed at least one period on 2G oral semaglutide and one period on 1G oral semaglutide BMI body mass index, N/n number of participants, SD standard deviation Bioequivalence of Pharmacokinetic Endpoints Semaglutide dosing interval profiles at SS for each dose comparison (9 vs 14 mg [group 1], 4 vs 7 mg [group 2] and 1.5 vs 3 mg [group 3]) are shown in Fig

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