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Oral bioavailability for Dihexa has been estimated at 4060% in animal models, substantially higher than most peptides which typically show less than 5% oral absorption due to first-pass metabolism and enzymatic degradation in the gastrointestinal tract

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Multiple clinical studies indicate the essential role of intestinal flora perturbations in the occurrence and development of IBD (60)

AOD 9604 is valuable because it specifically targets lipid metabolism pathways without broad hormonal interference