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The t 1/2, ss was comparable between two dose groups, with geometric means of 153 and 161 h in healthy subjects receiving 20 and 40 mg respectively, which is similar to semaglutide administered subcutaneously, suggesting that the elimination phase of oral semaglutide is comparable with that observed with subcutaneous administration
A Comprehensive Review of the Pharmacologic Management of Uterine Leiomyoma
M.WuY.et al (2010)
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