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The prespecified bioequivalence criteria according to EMA, FDA and PMDA guidelines were met across the three investigated dose levels of 2G versus 1G oral semaglutide (9 mg vs 14 mg, 4 mg vs 7 mg, 1.5 mg vs 3 mg) (Table 2)

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Myint, P.K., et al

COVID patients and controls were excluded if they had a lifetime history of psychiatric axis-1 disorders, including major affective disorders such as major depression and bipolar disorder, dysthymia, GAD and panic disorder, schizo-affective disorder, schizophrenia, psycho-organic syndrome, and substance use disorders, except tobacco use disorder (TUD)