SWISS peptide
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AED 599AED 29.95 / mg

1 vial × AED 599 · Total AED 599

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20 mg vial · Most popular

One vial containing 20 mg of Retatrutide. The most popular format in the range.

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Delivery & packaging

Worldwide delivery in 3–5 business days. Free delivery with the 40 mg vial. Transport conditions must be confirmed before ordering.

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Third-party laboratory testing

Check the laboratory identity and batch number on the certificate of analysis.

The compound

What Is Retatrutide?

Retatrutide (LY-3437943) is an investigational triple receptor agonist peptide. It activates three metabolic receptors: GLP-1 (glucagon-like peptide 1), GIP (glucose-dependent insulinotropic polypeptide), and glucagon.

Its combined receptor activity is being investigated in controlled research programmes. Published studies describe the investigational compound; they do not validate the identity or performance of a separately supplied research product.

  • GLP-1Glucagon-like peptide 1
  • GIPGlucose-dependent insulinotropic polypeptide
  • GlucagonGlucagon receptor
Retatrutide remains investigational. Clinical trial findings below are research context, not a claim of clinical efficacy for this vial or a recommendation for human or animal use. This product is supplied exclusively for in vitro scientific research.

2023 · Phase 2 · Peer-reviewed

48-week trial findings

In the Phase 2 trial published in The New England Journal of Medicine, the 12 mg retatrutide group had a least-squares mean body-weight change of −24.2% at 48 weeks, compared with −2.1% with placebo.

Read the NEJM publication (opens in a new tab)

May 2026 · Phase 3 · Sponsor-reported

TRIUMPH-1 and its extension

Lilly’s May 2026 topline announcement reported average weight changes at 80 weeks of −19.0% with 4 mg, −25.9% with 9 mg, and −28.3% with 12 mg, compared with −2.2% with placebo.

In a prespecified 104-week extension among participants with baseline BMI ≥35, the 12 mg group reached an average −30.3% weight change. These figures were announced by the sponsor as topline results; the study groups and quantities are not instructions for use.

Read Lilly’s trial announcement (opens in a new tab)

Format, documentation & delivery

Why Choose Swiss Peptide
Retatrutide Vials?

Vial format.

Choose a vial containing 10 mg, 20 mg or 40 mg of Retatrutide to match the total quantity required for your in vitro research. Each unit contains one vial in the selected format.

≥99% purity specification.

Review the measured purity in the certificate for the exact batch supplied. Analytical panels may include identity, HPLC purity, endotoxin, heavy metals and net peptide content, where applicable. Each result should identify its laboratory and method.

Review batch documentation

Batch-specific verification.

Check that the analytical report matches the vial format and the exact batch you receive.

Research-grade packaging.

Keep the vial with its original packaging and batch information. Cold-chain insulated packaging supports the +2 to +8°C transport range. Keep the packaging and product information together, and follow the storage conditions specified for the batch.

Confirm the supplied accessories and batch documents before ordering.

Worldwide delivery.

Worldwide delivery in 3–5 business days.

Cold-chain shipping maintains the +2 to +8°C range during delivery.

40 mg vial
Free delivery
Other orders below AED 1,000
AED 50
Orders from AED 1,000
Free delivery

Sourcing & batch traceability.

A traceable product links its packaging, batch reference and analytical documentation. Review the source, packing details and report reference for the actual batch before ordering.

No Swiss Peptide batch report is currently published on this page. Reports issued for another supplier or batch cannot verify this product.

Check documentation availability

Three receptor pathways

How Retatrutide Works —
Triple Receptor Mechanism

Retatrutide activates GLP-1, GIP and glucagon receptors. Laboratory studies investigate how these three pathways contribute to its pharmacology. The descriptions below concern receptor biology and published research, not established effects of this vial.

GLP-1 (glucagon-like peptide 1) receptor

GLP-1 receptor signalling is involved in appetite regulation and glucose-dependent insulin secretion. GLP-1 receptor agonists can also slow gastric emptying. This receptor is targeted by semaglutide and is one of the two receptor targets of tirzepatide.

GIP (glucose-dependent insulinotropic polypeptide) receptor

GIP is an incretin pathway involved in glucose-dependent insulin secretion. Retatrutide and tirzepatide both activate the GIP receptor alongside GLP-1 receptors; retatrutide additionally activates the glucagon receptor.

Glucagon receptor

Glucagon-receptor activation is the third component of retatrutide’s receptor profile. In the original discovery study, this component increased energy expenditure in obese mice. That preclinical finding does not establish the same independent effect in humans or demonstrate the performance of a separately supplied product.

Understanding the differences

Retatrutide vs Tirzepatide vs Semaglutide — Research Comparison

A reference to receptor targets and selected published trials. The studies below used different populations, durations and statistical analyses; their results are not a head-to-head comparison or a prediction of individual outcomes.

Swipe horizontally to compare all three compounds.

Receptor profiles and selected trial results for retatrutide, tirzepatide and semaglutide.
Research characteristicRetatrutideTirzepatideSemaglutide
Receptor targetsGLP-1 + GIP + glucagonGLP-1 + GIPGLP-1
MechanismTriple receptor agonistDual receptor agonistSingle receptor agonist
Selected published trialPhase 2 · 48 weeksNEJM · 2023 (opens in a new tab)SURMOUNT-1 · 72 weeksNEJM · 2022 (opens in a new tab)STEP 1 · 68 weeksNEJM · 2021 (opens in a new tab)
Mean body-weight change in the cited study group−24.2%12 mg study group; −2.1% with placebo.−22.5%15 mg group, efficacy estimand; −2.4% with placebo. The treatment-regimen estimand was −20.9% versus −3.1%.−14.9%2.4 mg study group; −2.4% with placebo.
Glucagon-receptor activityIncluded in its receptor profile.Glucagon-linked energy expenditure was demonstrated in the preclinical mouse study.Not a target in its described receptor profile.Not a target in its described receptor profile.
Development / authorised-product contextInvestigational; Phase 3 TRIUMPH programme.Approved prescription products exist, including Zepbound in the US.Approved prescription products exist, including Wegovy in the US.

How to read these figures. They are group averages from separate trials, not maximum possible results. An estimand defines how a treatment effect is calculated, including how discontinuation is handled. Study-group amounts identify the published evidence and are not dosing recommendations. Approval of a named prescription medicine does not extend to research products sold separately.

Study context & documentation

Research Protocol Reference

Different research settings answer different questions. Use the original publication and its methods to understand each study; clinical trial schedules are not instructions for using this research product.

Swipe horizontally to read the full reference.

Retatrutide research settings, study timeframes and documentation references.
Research settingStudy timeframeReference & interpretation
In vitro receptor assaysAssay-specificExamine receptor activity under defined laboratory conditions. Record the assay method, controls and batch documentation.Read the discovery study (opens in a new tab)
Phase 2 clinical study48 weeksA controlled clinical trial with eligibility criteria, predefined treatment groups and safety monitoring. Its protocol does not establish a self-administration schedule.Read the Phase 2 publication (opens in a new tab)
Phase 3 TRIUMPH-180 weeks104-week extension in a prespecified subgroupA separate investigational trial programme. Review the study population, endpoints and analysis before interpreting sponsor-reported findings.Read the trial announcement (opens in a new tab)

For in vitro scientific research only. This product is not intended for human or animal consumption, or for therapeutic, diagnostic or cosmetic use. The 10 mg, 20 mg and 40 mg options indicate total vial content, not a weekly dose or treatment schedule.

Product specifications

The details that matter.

Retatrutide supplied in a vial. Choose the total quantity contained in each vial: 10, 20 or 40 mg.

Documentation comes first.

The certificate of analysis (COA) and HPLC data must match the batch you receive. Check their availability before ordering.

Chemical designation
Retatrutide (LY-3437943)
Product format
Vial containing 10, 20 or 40 mg of Retatrutide
Selected quantity
20 mg · 1 × 20 mg vial
Purity
≥ 99% Target specification. The measured value must be confirmed by the batch COA.
Testing
Certificate of analysis (COA) / HPLCAvailability and the third-party laboratory must be confirmed for the relevant batch.
Storage
Store between +2 and +8 °C, protected from light.Keep in the box and follow the storage conditions and shelf life specified in the batch documentation.
Permitted use
For in vitro scientific research only
≥ 99 %

Target purity specification

One specification. One reference document.

Purity is no substitute for traceability. The batch certificate identifies the analytical method, results and laboratory. This document is required to verify compliance with the stated specification.

Good to know

Your questions.
Our answers.

Useful information to help you choose a format and review the documentation.

This product is intended exclusively for in vitro scientific research in a suitable laboratory environment. It is not intended for human or animal consumption, or for therapeutic, diagnostic or cosmetic use.

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Analytical documentation

Before ordering, request the COA and HPLC results that match the exact batch in question.

No batch report published yet

The ≥ 99% purity specification must be verified in the batch-specific certificate. No third-party laboratory is stated to have certified this product.

The analytical documentation should allow you to verify: