Retatrutide 40 mg pen — analytical-grade research peptideLY-3437943 · 40 mg / 3 mL pen
Fig. 01 · Specimen
Pre-filled pen
In the box
  • ·Pre-filled 40 mg / 3 mL pen
  • ·Alcohol swabs
MetabolicClass IIILY-3437943Zapopharma Reta Pen

Retatrutide 40 mg pen

Triple-receptor agonist — pre-filled research pen, 4 × 10 mg.

Retatrutide is a triple agonist at the GLP-1, GIP, and glucagon receptors. The 40 mg pen is the highest-dose presentation in the Omega Grade catalogue — pre-reconstituted for researchers running extended protocols.

Designation
LY-3437943
CAS no.
2381089-83-2
Molecular formula
C221H343N51O66
MW (Da)
4729.4
Residues
39
Purity
≥ 99.2%
Form
Pre-filled pen
Dose
40 mg / 3 mL pen
Class
Class III
Dispatch · per unit
£249GBP
≈ €294 · 0.00461 BTC
1
In stock·Same-day dispatch (order by 09:30 UK)·Tracked24 Royal Mail £6.50·Not shipped to USA
Clinical status: Investigational. Phase 3 trials (TRIUMPH programme, Eli Lilly). Not approved by any regulatory authority for any indication.
§ A Overview

What the peptide is.

Retatrutide (LY-3437943) is an investigational once-weekly triple agonist at the GLP-1, GIP, and glucagon receptors, currently in Phase 3 (TRIUMPH programme) under Eli Lilly. The 39-amino-acid peptide carries a C20 fatty-diacid moiety that extends plasma half-life via albumin binding.

The pre-filled pen presentation matches the clinical format used in investigational trials. Omega Grade supplies lyophilised active peptide in clinical-grade pens sourced from Zapopharma, manufactured to a ≥ 99.2% purity specification verified independently by Janoshik Analytical.

Retatrutide is not approved anywhere and is not a medicine. The material is strictly for in vitro research, analytical method development, and reference-standard use.

Proposed mechanism

Dose-dependent agonism at the GLP-1, GIP, and glucagon receptors. The GLP-1 and GIP components are shared with tirzepatide; the added glucagon-receptor agonism is proposed to increase energy expenditure and hepatic fatty-acid oxidation in preclinical models.

§ B Laboratory handling

Reconstitution, storage, and handling.

Lab-technical guidance for the researcher handling the material. Not therapeutic dosing, not administration guidance — those are not within the scope of this supply.

Reconstitution
Recommended solvent
Pre-reconstituted — no solvent required
Typical volume
N/A (pen)
Notes
  • The pen is shipped cold-chain and must be refrigerated on receipt.
  • Gentle swirl if any settling is observed before first use.
Storage
Lyophilised
Pre-filled pen — store 2–8 °C. Pen is shipped cold-chain; after first use it may be kept at 2–8 °C.
Reconstituted
Pens are pre-reconstituted. Once opened, use within the manufacturer-stated window (typically 4 weeks refrigerated).
Shelf life · sealed
See pen label — typically 18–24 months sealed under refrigeration.
Shelf life · reconstituted
Once pen is opened: ~4 weeks at 2–8 °C.
Handling notes
  • Cold-chain dispatch. Temperature logger included.
  • Do not freeze the pen — freeze-thaw compromises pen mechanics.
  • Discard sharps in compliant container.
§ C Certificate of Analysis

This lot, documented.

Every shipment is accompanied by a signed four-page analytical report including the HPLC chromatogram, ESI-MS spectrum, purity calculation, and sample handling chain-of-custody.

The report you will receive is specific to the lot dispatched to you. The display below is a current representative example.

retatrutide 40mg pen · batch.log
LIVE
04:22:11lot 26-04-A received ┈ 5.00 g
04:22:40weight check ┈ PASS ±0.4 mg
04:23:12sample → janoshik ┈ 50 mg
04:23:12tracking #jnk-9218334
05:18:03HPLC result ┈ 99.24 %
05:18:04MS obs 4729.42 Da ┈ PASS
05:18:05coa.pdf signed ┈ attached
05:18:06lot approved ┈ LIVE
janoshik.report.txt
SIGNED
REPORT ID     JA-26-04-012
SUBJECT       Retatrutide 40 mg pen
DESIGNATION   LY-3437943
LOT           26-04-A
METHOD        RP-HPLC, ESI-MS
COLUMN        C18, 250 x 4.6 mm, 5 um
MOBILE PHASE  A: 0.1% TFA in H2O
              B: 0.1% TFA in ACN
GRADIENT      5 -> 65% B over 20 min
FLOW RATE     1.0 mL/min
DETECTION     UV 214 nm
INJECTION     20 uL @ 0.5 mg/mL
---
PURITY (A%)   99.20
MASS EXP.     4729.40 Da
MASS OBS.     4729.42 Da
---
CONCLUSION    Identity CONFIRMED · Purity PASS
SIGNED BY     J. Novak, MSc · Janoshik Analytical SVK
DATE          2026-04-11
representative chromatogram · A214 nmRT 8.42 min
Representative trace · Lot-specific COA included with every dispatch
purity≥ 99.2%
§ D Clinical trials

Registered clinical investigation.

Links below resolve to the ClinicalTrials.gov registry. Trial status reflects publicly disclosed information at the time of publication.

NCTPhaseTitleStatus
NCT05929066Phase 3TRIUMPH-1: Retatrutide in obesityOngoingRegistry ↗
NCT05936151Phase 3TRIUMPH-OUTCOMES: cardiovascular outcomesOngoingRegistry ↗
§ E Peer-reviewed studies

Research references for Retatrutide 40 mg pen.

3 peer-reviewed publications. Links resolve to PubMed. DOIs are provided where available.

  1. [01]
    Jastreboff AM, Kaplan LM, Frías JP, et al.

    Triple-Hormone-Receptor Agonist Retatrutide for Obesity — A Phase 2 Trial

    New England Journal of Medicine · 2023
  2. [02]
    Rosenstock J, Frias J, Jastreboff AM, et al.

    Retatrutide, a GIP, GLP-1 and glucagon receptor agonist, for people with type 2 diabetes

    The Lancet · 2023
  3. [03]
    Coskun T, Urva S, Roell WC, et al.

    LY3437943, a novel triple glucagon, GIP, and GLP-1 receptor agonist

    Cell Metabolism · 2022
§ F Questions

About this peptide.

For general site, shipping, and payment questions see the full FAQ.

Q.Why is this supplied as a pen rather than a vial?
A.The pen format matches the clinical formulation used in Eli Lilly's Phase 3 investigational trials, making it the closest-to-reference analytical standard available in research supply. It is pre-reconstituted and cold-chain shipped.
Q.Is the pen identical to the TRIUMPH clinical device?
A.The active peptide and basic delivery format are equivalent. It is not a clinical device and is not intended for human administration.
Research use only

This peptide is supplied by Omega Grade for in vitro laboratory research use. It is not a drug, food, cosmetic, or dietary supplement. It is not approved by the FDA, EMA, MHRA, PMDA, or any other regulatory authority for any therapeutic indication.

No claim of therapeutic benefit is made or implied. The material is not intended for human or veterinary consumption, administration, or any form of self-experimentation. By purchasing, you acknowledge the researcher terms and accept full responsibility for local import compliance and all handling.