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Retatrutide 10mg Easy Pen
Triple GLP-1/GIP/glucagon agonist — weight, glycemic & metabolic research
SKU: EP-RET-10-1
99% Purity$280
- Format
- Easy Pen
- Dosage
- 0.05mg per click
- Capacity
- 10 mg
Potential benefits
- Weight-reduction research
- Glycemic-control research
- Liver-fat & liver-health research
- Cardiometabolic-marker research
- Body-composition research
- Weekly subcutaneous dosing
Retatrutide is an investigational peptide therapy designed to activate three critical metabolic receptors—GLP-1, GIP, and glucagon. In research, this triple-agonist approach engages the body’s natural metabolic signaling pathways, with studied effects on fat loss, blood-sugar regulation, liver health, and inflammation. Its multi-hormone mechanism is studied not only for appetite suppression but also for effects on energy expenditure, visceral and liver fat, and cardiometabolic markers.
In clinical trials, Retatrutide showed among the highest weight-reduction results recorded in clinical research for a non-surgical agent, while also addressing underlying drivers of metabolic disease. Retatrutide is a multi-receptor agonist, meaning it activates three hormone pathways simultaneously:
GLP-1 (Glucagon-like Peptide-1): Promotes satiety, slows gastric emptying, and enhances glucose-stimulated insulin secretion.
GIP (Glucose-dependent Insulinotropic Polypeptide): Enhances insulin release in response to meals and synergizes with GLP-1 to improve metabolic response.
Glucagon Receptor: Stimulates fat oxidation, increases energy expenditure, and reduces liver fat stores.
In study settings, these pathways have been associated with shifts in energy balance, reduced food intake, fat-store reduction, and changes in metabolic biomarkers relative to single-pathway agents.
In clinical trials, Retatrutide showed among the highest weight-reduction results recorded in clinical research for a non-surgical agent, while also addressing underlying drivers of metabolic disease. Retatrutide is a multi-receptor agonist, meaning it activates three hormone pathways simultaneously:
GLP-1 (Glucagon-like Peptide-1): Promotes satiety, slows gastric emptying, and enhances glucose-stimulated insulin secretion.
GIP (Glucose-dependent Insulinotropic Polypeptide): Enhances insulin release in response to meals and synergizes with GLP-1 to improve metabolic response.
Glucagon Receptor: Stimulates fat oxidation, increases energy expenditure, and reduces liver fat stores.
In study settings, these pathways have been associated with shifts in energy balance, reduced food intake, fat-store reduction, and changes in metabolic biomarkers relative to single-pathway agents.
- Participants in a 48‑week Phase 2 study lost up to 24.2% of initial body weight at higher doses.
- Significant reductions in HbA1c and fasting glucose were observed in adults with obesity ± type 2 diabetes, outperforming monotherapies.
- Over 80% of participants achieved ≥70% reduction in liver fat; >85% resolved steatosis in a MASLD subgroup.
- Reductions in blood pressure, triglycerides, LDL, and inflammatory biomarkers were reported among trial participants.
- Body-composition data reported a greater proportion of fat-mass loss relative to lean-mass loss in study participants
- Long half-life (~6 days) allows comfortable once‑weekly subcutaneous injections.
References
- Triple–Hormone-Receptor Agonist Retatrutide for Obesity – A Phase 2 Trial
- Retatrutide in patients with obesity and MASLD
- Body composition outcomes of Retatrutide in patients with obesity
- Retatrutide in type 2 diabetes – efficacy and glucose response
- Sub-analysis of the Phase 2 trial in Nature Medicine
- ClinicalTrials.gov: Ongoing global studies on weight loss, cardiovascular risk, and diabetes outcomes
| Molecular formula | C221H342N46O68 |
|---|---|
| Molecular weight | 4800 Da |
| CAS number | 2381089-83-2 |
| Purity | 99% |
| Storage | Use within 30 days of first use. Store at 2–8°C / 35–46°F. Protect from sunlight. Do not freeze. |
Synonyms: Retatrutide, 2381089-83-2, EX-A7826E, GTPL13769
Research & background
Independent, research-focused reading. Educational references, not medical advice or product claims.




