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Creatinine levels remained relatively stable in the GLP-1 while increasing from 2.2 mg/dL at baseline to 2.74 mg/dL at 6 months for adults not using a GLP-1

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Program:12 Week Program

Single-Mechanism Peptides AOD 9604: Modified fragment of growth hormone Targets fat metabolism without affecting blood sugar Modest weight loss effects (typically 2-6%) Minimal side effects AOD 9604 research shows promise for targeted fat reduction 5-Amino-1MQ: Inhibits NNMT enzyme to boost NAD+ levels Enhances cellular metabolism and energy production Supports weight management through metabolic optimization Well-tolerated with few reported side effects 5-Amino-1MQ research demonstrates metabolic benefits Dual-Mechanism Approaches Tirzepatide (GIP/GLP-1 dual agonist): Activates both GIP and GLP-1 receptors Achieved ~15-22% weight loss in clinical trials FDA-approved for type 2 diabetes and obesity Represents current standard for dual-mechanism therapy CagriSema (Cagrilintide/Semaglutide): Combines amylin and GLP-1 activation Demonstrated 15.6% weight loss in phase 3 trials Regulatory submissions completed in 2024 Establishes proof-of-concept for cagrilintide combinations The Four-Pathway Advantage The theoretical cagrilintide blend with retatrutide would represent the most comprehensive multi-pathway approach studied to date: Receptor Targets: Amylin (cagrilintide) – Satiety and gastric emptying GIP (retatrutide) – Insulin secretion and fat metabolism GLP-1 (retatrutide) – Appetite suppression and glucose control Glucagon (retatrutide) – Energy expenditure and fat oxidation This four-pathway activation potentially addresses metabolic health more comprehensively than any existing single agent or combination