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Key areas of concern for decision makers and executives include: Continued rapid rates of increased utilization: Treatment guideline recommendations to prefer GLP-1 agonists and GIP/GLP-1 dual agonists over other less expensive diabetic treatments Increase in physicians awareness of obesity as a disease Stronger trust in the long-term effects and safety of GLP-1 receptor agonists Unwavering demand by individuals seeking quick weight loss solutions Additional products seeking approval and entering the market: Over 50 products are currently in clinical development for obesity and/or T2D GLP-1 agonism is being studied in combination with other mechanisms of action including GIP agonism, glucagon agonism, amylin agonism, and PYY agonism Shortages of currently marketed drugs provide opportunity for additional products to successfully enter the marketplace Additional indications for these products are gaining approval: Clinical trials are ongoing for several indications beyond the currently approved obesity and/or T2D uses Examples of therapeutic applications currently under investigation include Parkinsons and Alzheimers diseases, smoking cessation, alcoholism, and MASH The GLP-1 agonist market is rapidly evolving with significant implications for payers

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Meals built around lean proteins, cooked vegetables, whole foods, and healthy fats tend to be best tolerated

A stepwise-regimen of combining amylin pharmacotherapy with liraglutide strongly suppress energy intake and body weight gain in DIO rats While several studies have described the intake and body weight suppressive effects of liraglutide and sCT administration as monotherapies 21,22,43,45 , a direct comparison of the chronic food intake and body weight suppressive effects of amylin and GLP-1R analogs administered individually or in a combination is still lacking

Who This Is For: Anyone following a GLP-1 weight loss approach

In addition to that, DPP-4 enzyme also deactivates more than 40 physiologically active hormones, neuropeptides, cytokines, and other proteins in vivo through dipeptide cleavage (Mentlein et al., 1993)