Retatrutide
A GLP-1/GIP/GCG receptor agonist for weight loss and metabolic health.
Retatrutide is a cutting-edge
Retatrutide is a cutting-edge investigational drug designed to address obesity and type 2 diabetes through a triple hormone approach.
GLP-1 (Glucagon-Like Peptide-1)** – reduces appetite and improves insulin response
GIP (Glucose-Dependent Insulinotropic Polypeptide)** – supports insulin secretion and metabolic balance
Glucagon receptor – boosts energy expenditure and fat burning
Benefits
Explore the most important features we have
Improves Insulin Sensitivity
Appetite Suppression
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Targets Visceral Fat
Increases Energy Use
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Cardiometabolic Support
Reduces Inflammation
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This combination helps regulate hunger, stabilize blood sugar, and accelerate weight loss. By mimicking the body’s natural hormonal signals, Retatrutide provides a more comprehensive metabolic effect compared to traditional GLP-1-only drugs.
Alexandre Pop, Head of Marketing
Research + Clinical Study Snippets
We've got answers!
Over 24% weight reduction in clinical trial participants
Participants in phase 2 trials lost more than 24% of their body weight over 48 weeks — a record-high response in obesity treatment trials.
Significant reduction in HbA1c in T2D patients
Retatrutide showed strong glucose-lowering effects, with major reductions in HbA1c in patients with type 2 diabetes, alongside weight loss.
Safe and well-tolerated in trials
Most side effects were mild to moderate (like nausea), and similar to those seen with other incretin-based therapies.
Triple hormone mechanism improves metabolic regulation
Activating GLP-1, GIP, and glucagon receptors leads to appetite suppression, enhanced insulin sensitivity, and increased fat metabolism.
Retatrutide Kits / Vials
Retatrutide is a novel multi-receptor agonist that targets the GLP-1, GIP, and glucagon receptors to deliver powerful benefits in weight reduction, blood sugar control, and overall metabolic regulation. By combining these three hormonal pathways, Retatrutide offers a more comprehensive approach than existing single-pathway therapies.
