Additionally, co-administration of this antagonist with a GLP-1 receptor agonist in DIO mice potentiated weight loss compared to either monotherapy ( Latest in 2024, AT-7687, an optimized peptide analogue of the naturally occurring GIP(3-30)NH 2 was characterized as a potent and selective GIP receptor antagonist ( Table 1 ) with a circulatory half-life of 27.4 hours ( Figure 3 )
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individual results vary These are averages from controlled clinical trials
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