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A few GLP-1 agonists currently in phase 3 trials are higher-dose injectable semaglutide 7.2 mg (Novo Nordisk), oral semaglutide 50 mg (Novo Nordisk) and orforglipron (Eli Lilly)
In two randomized controlled clinical trials, inulin ingestion did not change appetite, intestinal permeability, or levels of inflammatory biomarkers, but caused flatulence and soft stools (122, 124)

Energy expenditure (possible): Some evidence amylin may increase energy expenditure Not as strong as mechanism Minor contributor if real Why amylin is effective for obesity Physiologic rationale: Amylin naturally controls meal size Obesity often associated with amylin resistance Type 2 diabetics have reduced amylin Replacing/supplementing amylin restores control Addresses root cause Synergy with insulin: Both co-secreted normally Work together to regulate feeding Amylin prevents overeating Insulin handles glucose Complementary hormones Comparison to GLP-1 mechanisms: GLP-1: Moderate gastric slowing, strong central appetite effects Amylin: Very strong gastric slowing, moderate central effects Different receptor pathways Complementary not redundant Can combine for synergy Get personalized weight loss protocols at SeekPeptides using our peptide calculator and peptide cost calculator