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For FDA bioequivalence analysis, as the estimated within-participant standard deviation for oral semaglutide, s(WR), was ≥ 0.294 for both co-primary endpoints, the reference-scaled average bioequivalence (RSABE) analysis was the primary analysis for AUC 0–24h,SS and C max, 0–24h,SS [34]
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Form:Capsules
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