
Retatrutide
LY3437943
Retatrutide is a novel triple hormone receptor agonist that simultaneously activates GLP-1, GIP, and glucagon receptors for superior metabolic effects. This innovative approach produces enhanced appetite suppression, improved insulin sensitivity, and increased energy expenditure, potentially delivering 20-25% weight loss in clinical trials.
Complete Research Database
Dual Receptor Mechanism (GIP/GLP-1)
GLP-1 Receptor Pathway
- •Increases insulin secretion (glucose-dependent)
- •Suppresses glucagon release
- •Slows gastric emptying
- •Enhances satiety in hypothalamus
- •Preserves beta-cell function
GIP Receptor Pathway
- •Enhances insulin secretion (stronger than GLP-1)
- •Promotes fat oxidation
- •Improves insulin sensitivity in muscle
- •Reduces hepatic glucose production
- •Modulates adipose tissue metabolism
Why Dual Agonism is Superior
Retatrutide functions as a triple agonist targeting GLP-1, GIP, and glucagon receptors simultaneously. GLP-1 receptor activation provides appetite suppression and glucose-dependent insulin secretion. GIP receptor engagement enhances insulin sensitivity and promotes satiety. Glucagon receptor stimulation increases energy expenditure and promotes fat oxidation. This synergistic triple mechanism creates superior metabolic effects compared to single or dual agonist therapies.
Pharmacokinetic Profile
Top 10 High-Quality Research Articles
Retatrutide for Obesity - A Phase 3 Randomized Controlled Trial (TRIUMPH-1)
ReadRetatrutide in Type 2 Diabetes and Obesity (TRIUMPH-2)
ReadLong-term Safety and Efficacy of Retatrutide
ReadMedical Disclaimer
Retatrutide is currently in Phase 3 clinical trials and is not yet FDA approved. This information is for educational purposes only and should not replace medical advice. Consult with healthcare providers familiar with investigational therapies for personalized guidance. Side effects and contraindications are based on available clinical trial data.