Retatrutide 40MG

$140.00

20 in stock

Dosage Information

  • Reconstitute: Add 2.0 mL bacteriostatic water → ~20.0 mg/mL concentration.
  • Typical weekly range: 2–8 mg once weekly (gradual escalation over 8–12 weeks).
  • Easy measuring: At 20.0 mg/mL, 1 unit = 0.01 mL ≈ 200 mcg on a U-100 insulin syringe.

Storage: Lyophilized: freeze at −20 °C (−4 °F); after reconstitution, refrigerate at 2–8 °C (35.6–46.4 °F) for up to 4 weeks

Week Daily Dose (mcg) Units (per injection) (mL)
Weeks 1–4 2 mg (2000 mcg) 10 units (0.10 mL)
Weeks 5–8 4 mg (4000 mcg) 20 units (0.20 mL)
Weeks 9–12 6 mg (6000 mcg) 30 units (0.30 mL)
Weeks 13+ 8 mg (8000 mcg) 40 units (0.40 mL)

Product Description:

Retatrutide (also known as LY3437943) is an investigational synthetic peptide developed by Eli Lilly. It is a triple receptor agonist designed to simultaneously activate three key hormone receptors: GLP-1 (glucagon-like peptide-1), GIP (glucose-dependent insulinotropic polypeptide), and glucagon (GCGR).

It is a single peptide molecule with a fatty acid modification (acylation) that extends its half-life, allowing for once-weekly subcutaneous injections.

How It Works

Retatrutide’s triple-agonist mechanism targets multiple metabolic pathways for synergistic effects:

  • GLP-1 receptor activation: Suppresses appetite, slows gastric emptying, enhances insulin secretion (glucose-dependent), and promotes satiety.
  • GIP receptor activation: Improves insulin sensitivity, supports fat metabolism, and further enhances appetite regulation (building on the success of dual agonists like tirzepatide).
  • Glucagon receptor activation: Increases energy expenditure (calorie burning), promotes lipolysis (fat breakdown), and helps reduce liver fat, while being balanced to avoid excessive hyperglycemia.

This multi-pathway approach leads to greater appetite suppression, improved glucose control, increased metabolic rate, and significant fat loss (especially visceral and liver fat) compared to single or dual agonists.

Potential Benefits and Why People Use It

In clinical trials (Phase 2 and early Phase 3 data as of 2026), retatrutide has shown impressive results, often outperforming existing options:

  • Substantial weight loss: Up to ~24% body weight reduction at 48 weeks in Phase 2 (higher doses), and around 28% in some Phase 3 reports at longer durations — approaching or exceeding bariatric surgery outcomes for many participants.
  • Improved metabolic health: Better glycemic control (HbA1c reductions), reduced liver fat (beneficial for NAFLD/NASH), improved lipid profiles, and lower blood pressure.
  • Additional benefits: Potential improvements in cardiovascular risk factors, sleep apnea, osteoarthritis pain, and overall body composition.

It is primarily researched for obesity, type 2 diabetes, and related metabolic conditions. Its triple action makes it a promising “next-generation” option after semaglutide (GLP-1 only) and tirzepatide (GLP-1 + GIP).

Important Caveats

  • Regulatory status: Not FDA-approved as of mid-2026. It remains investigational, with Phase 3 trials ongoing and potential approval projected for late 2026–2027. Research-grade or compounded versions carry quality and legal risks.
  • Side effects: Primarily gastrointestinal (nausea, vomiting, diarrhea, constipation) — common with this class, often during dose escalation. Other possible effects include increased heart rate, injection-site reactions, or fatigue. Generally well-tolerated with low discontinuation rates in trials, but monitoring is essential.
  • Safety: Long-term data is still emerging. Not suitable for everyone (e.g., contraindicated in certain thyroid or pancreatic conditions). Banned by WADA for athletes.

Bottom line: Retatrutide represents a significant advancement in weight-management peptides due to its triple-agonist design, delivering potentially superior weight loss and metabolic benefits. For your EDB LLC peptide products, emphasize its research/experimental status, high-purity sourcing, strong disclaimers, and the critical need for professional medical supervision. As with your other offerings (BPC-157, TB-500, IGF-1 LR3, Tesamorelin, MOTS-c, CJC-1295/Ipamorelin, etc.), position it educationally within a research context. Always recommend consulting a qualified healthcare professional before considering use.

 

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