Scientific molecular DNA helix background for Retatrutide research peptide
Research Peptide — 20mg

Retatrutide
20mg

by OzR3ta

The world's first triple-action receptor agonist targeting GLP-1, GIP, and Glucagon pathways. Premium research-grade peptide with unmatched purity.

24%
Avg. Weight Reduction
Triple
Receptor Agonist
99%+
Purity Guaranteed
Retatrutide 20mg RT20 OzR3ta branded vial
Concentration
20mg/vial
Purity
≥99%
Triple-Action Mechanism

Three Receptors. One Molecule.

Retatrutide (LY-3437943) is the world's first triple-receptor agonist, simultaneously activating GLP-1, GIP, and Glucagon pathways for unprecedented metabolic research potential.

GLP-1

Glucagon-Like Peptide-1

Reduces appetite, slows gastric emptying, and enhances insulin secretion. The primary pathway responsible for significant weight reduction and improved glycemic control.

GIP

Glucose-Dependent Insulinotropic Polypeptide

Amplifies insulin response, enhances fat metabolism, and works synergistically with GLP-1 to improve metabolic outcomes beyond what single-agonist compounds can achieve.

Glucagon

Glucagon Receptor

Increases resting energy expenditure, promotes hepatic fat oxidation, and drives liver fat reduction. This unique third pathway sets Retatrutide apart from all existing compounds.

~4,200 Da
Molecular Weight
Subcutaneous
Administration
Once Weekly
Frequency
Lyophilized
Form
Research-Backed Benefits

Why Retatrutide 20mg Stands Apart

Backed by rigorous clinical research and published in the New England Journal of Medicine, Retatrutide's triple-action mechanism delivers a comprehensive range of metabolic benefits that no single or dual-agonist compound can match.

Up to 24%
body weight loss

Significant Weight Reduction

Clinical trials have demonstrated that Retatrutide produces substantial and dose-dependent weight loss. In the Phase 2 NEJM-published trial, participants receiving the highest dose achieved an average weight reduction of up to 24% at 48 weeks — surpassing results seen with single or dual-agonist compounds. This level of weight loss approaches what was previously only achievable through bariatric surgery.

Boosted
resting energy expenditure

Enhanced Fat Burning & Metabolism

Retatrutide's unique glucagon receptor activation increases resting energy expenditure, meaning your body burns more calories even at rest. This thermogenic effect promotes the oxidation of stored fat for energy, targeting both subcutaneous and visceral fat deposits. The triple-agonist mechanism creates a metabolic environment that favors sustained fat loss rather than muscle catabolism.

Dramatic
liver fat decrease

Visceral & Liver Fat Reduction

Research has shown Retatrutide produces remarkable reductions in visceral adipose tissue — the dangerous fat surrounding internal organs linked to metabolic disease. Additionally, studies have demonstrated significant decreases in liver fat content, suggesting potential benefits for metabolic-associated fatty liver conditions. The glucagon receptor component is particularly effective at mobilizing hepatic fat stores.

Improved
cardiometabolic markers

Cardiovascular Health Support

Retatrutide has shown promising improvements across multiple cardiovascular risk factors. Clinical data indicates meaningful reductions in systolic blood pressure, triglycerides, and LDL cholesterol, alongside improvements in HDL cholesterol levels. A dedicated Phase 3 cardiovascular outcomes trial (SELECT-TRIUMPH) is currently evaluating Retatrutide's ability to reduce major adverse cardiovascular events.

Significant
HbA1c reduction

Superior Blood Sugar Control

Through coordinated activation of GLP-1 and GIP receptors, Retatrutide enhances glucose-dependent insulin secretion and improves insulin sensitivity. Clinical studies in participants with Type 2 diabetes demonstrated clinically meaningful reductions in HbA1c levels. The multi-receptor approach provides more comprehensive glycemic control than single-pathway therapies, helping to stabilize blood sugar throughout the day.

Reduced
hunger & cravings

Appetite & Craving Regulation

Retatrutide works centrally in the brain to modulate appetite-regulating pathways. GLP-1 receptor activation in the hypothalamus reduces hunger signals and promotes satiety, while GIP receptor engagement helps regulate food reward pathways. Participants in clinical trials reported significantly reduced appetite, fewer food cravings, and improved portion control — making it easier to maintain a caloric deficit naturally.

Preserved
lean muscle mass

Improved Body Composition

Unlike many weight loss interventions that result in significant lean mass loss, Retatrutide's triple-agonist mechanism helps preserve lean body mass during weight reduction. The glucagon receptor activation promotes preferential fat oxidation, while the GIP pathway supports muscle protein synthesis. Clinical substudy data using body composition analysis (BIA) confirmed favorable changes in the ratio of fat mass to lean mass.

Favorable
tolerability data

Well-Tolerated Safety Profile

Across multiple clinical trials, Retatrutide has demonstrated an appropriate and manageable safety profile. The most commonly reported side effects were mild-to-moderate gastrointestinal symptoms (nausea, diarrhea, decreased appetite) that typically diminished over time with dose titration. No unexpected safety signals have emerged, and the compound continues to advance through Phase 3 clinical development.

Clinical Evidence

Backed by Rigorous Science

Retatrutide's efficacy is supported by peer-reviewed clinical trials published in the world's most prestigious medical journals, including the New England Journal of Medicine.

~24%
Weight Loss at 48 Weeks
Highest dose group
338
Participants in Phase 2
Randomized, placebo-controlled
Once Weekly
Dosing Frequency
Subcutaneous injection
28.7%
TRIUMPH-4 Result
Weight loss at 68 weeks

Clinical Development Timeline

2021Phase 1

Initial safety and tolerability established in healthy volunteers. Dose-dependent pharmacokinetics confirmed.

2023Phase 2

Published in NEJM — up to 24% weight loss at 48 weeks. Significant metabolic improvements across all dose groups.

2024–26Phase 3

TRIUMPH program — multiple large-scale trials evaluating efficacy in obesity, T2D, cardiovascular outcomes, and MASH.

Metabolic pathways illustration

Triple Metabolic Pathways

Retatrutide's unique mechanism activates three distinct metabolic pathways simultaneously, creating synergistic effects that amplify weight loss and metabolic improvement.

GLP-1
GIP
GCG
Key Publication

Jastreboff, A.M. et al. "Triple–Hormone-Receptor Agonist Retatrutide for Obesity — A Phase 2 Trial." New England Journal of Medicine, 2023.

Pricing

Premium Quality, Volume Savings

All vials are manufactured to the highest research-grade standards with ≥99% purity, verified by independent third-party testing. Bulk orders receive significant per-vial discounts.

Single Vial

1 vial — Retatrutide 20mg

$150/vial
  • 1 x Retatrutide 20mg Vial
  • Certificate of Analysis included
  • Secure packaging & shipping
  • Research-grade purity (≥99%)
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Research Pack

5 vials — Retatrutide 20mg

$125/vial
Total: $625
Save $125
  • 5 x Retatrutide 20mg Vials
  • Certificate of Analysis included
  • Secure packaging & shipping
  • Research-grade purity (≥99%)
  • Priority processing
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Lab Supply

10 vials — Retatrutide 20mg

$90/vial
Total: $900
Save $600
  • 10 x Retatrutide 20mg Vials
  • Certificate of Analysis included
  • Free express shipping
  • Research-grade purity (≥99%)
  • Priority processing
  • Dedicated support
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1 Vial$150
5 Vials$625 ($125/ea)
10 Vials$900 ($90/ea)
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Abstract scientific research background for OzR3ta Retatrutide peptide

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FAQ

Frequently Asked Questions

Everything you need to know about Retatrutide 20mg, from science to shipping.

Retatrutide (LY-3437943) is a novel triple-action receptor agonist peptide developed by Eli Lilly. It simultaneously activates three metabolic receptors: GLP-1 (glucagon-like peptide-1), GIP (glucose-dependent insulinotropic polypeptide), and glucagon receptors. This triple mechanism creates synergistic effects — GLP-1 reduces appetite and improves blood sugar control, GIP enhances insulin response and fat metabolism, while glucagon activation increases energy expenditure and promotes liver fat reduction.

Our Retatrutide 20mg vials are manufactured to research-grade standards with a purity of ≥99%, verified through independent third-party HPLC (High-Performance Liquid Chromatography) and mass spectrometry testing. Each order includes a Certificate of Analysis (CoA) documenting the exact purity, identity confirmation, and endotoxin levels of your specific batch.

For optimal stability, Retatrutide should be stored as a lyophilized (freeze-dried) powder at -20°C for long-term storage, or at 2-8°C (standard refrigerator temperature) for short-term storage up to several weeks. Once reconstituted with bacteriostatic water, the solution should be refrigerated at 2-8°C and used within 4 weeks. Avoid repeated freeze-thaw cycles and protect from direct light exposure.

In the landmark Phase 2 trial published in the New England Journal of Medicine (2023), participants receiving the highest dose of Retatrutide achieved an average weight reduction of approximately 24% at 48 weeks. The more recent TRIUMPH-4 Phase 3 trial demonstrated an average weight loss of 28.7% at 68 weeks. Additional benefits include significant reductions in liver fat, improvements in cardiovascular risk markers, and meaningful HbA1c reductions in participants with Type 2 diabetes.

While Semaglutide (Ozempic/Wegovy) is a single GLP-1 receptor agonist and Tirzepatide (Mounjaro/Zepbound) is a dual GLP-1/GIP agonist, Retatrutide is the first triple-agonist targeting GLP-1, GIP, and glucagon receptors. The addition of glucagon receptor activation provides unique benefits including increased resting energy expenditure and enhanced liver fat reduction. Clinical data suggests Retatrutide may produce greater weight loss than both alternatives.

In clinical trials, Retatrutide was administered as a once-weekly subcutaneous injection with a gradual dose escalation protocol. The titration typically starts at a lower dose and increases over several weeks to minimize gastrointestinal side effects. This product is sold strictly for research purposes. Please consult the relevant clinical literature and your institutional guidelines for specific dosing protocols.

Yes, we offer significant volume discounts. Our standard pricing tiers are: 1 vial at $150 each, 5 vials at $125 each ($625 total, saving $125), and 10 vials at $90 each ($900 total, saving $600). For orders exceeding 10 vials or for institutional/laboratory accounts, please contact us directly for custom wholesale pricing.

We accept Bitcoin (BTC) for fast, private transactions, as well as bank transfers. For Bitcoin, simply send payment to the wallet address provided on our payment page. For bank transfer details, please contact [email protected]. You can also reach us via Signal (@OzR3ta.33) or Threema (64S5X96V).

All orders are shipped in temperature-controlled, discreet packaging to maintain product integrity. Standard shipping is free and typically takes 3-5 business days. Express shipping is available for $10 with 2-3 business day delivery. Orders of 10+ vials qualify for free express shipping. We ship to most regions and provide tracking information for every order.