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Research-onlyVendors pendingFacts verified · 2026-05-25

GLP3-R + Cagrilintide Blend

GLP3-R + Cagrilintide is a compounded research-only blend combining retatrutide - Eli Lilly's investigational triple GLP-1/GIP/glucagon receptor agonist (LY3437943) - with cagrilintide, Novo Nordisk's long-acting amylin analog (AM833/NN0174-0833). The rationale parallels Novo Nordisk's CagriSema (cagrilintide plus semaglutide) but substitutes the more potent triple agonist. No clinical trial of this specific combination has been registered or completed; both components are themselves still investigational and not FDA-approved. Sold exclusively as a research chemical via compounding pharmacies and grey-market peptide vendors. All efficacy claims are extrapolated from the separate component trials.

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Formulation note

Retatrutide + Cagrilintide. Closest validated analog is CagriSema (cagrilintide + semaglutide, Novo Nordisk Phase III) — but distinct drug.

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Mechanism of action

The blend combines retatrutide, a unimolecular triple agonist at the GLP-1, GIP, and glucagon receptors (https://pubmed.ncbi.

The blend combines retatrutide, a unimolecular triple agonist at the GLP-1, GIP, and glucagon receptors (https://pubmed.ncbi.nlm.nih.gov/37366315/), with cagrilintide, a long-acting acylated amylin analog that agonizes amylin receptors AMY1/AMY2/AMY3 and the calcitonin receptor (https://pubmed.ncbi.nlm.nih.gov/34798060/). Retatrutide engages incretin (appetite suppression, slowed gastric emptying, glucose-dependent insulin release) and glucagon-mediated energy-expenditure pathways; cagrilintide adds central amylin signaling in the area postrema and hindbrain to amplify satiety and further delay gastric emptying. Mechanistically additive, the design parallels CagriSema (cagrilintide + semaglutide), substituting the more potent triple agonist. No clinical trials of this specific blend exist; mechanistic claims are extrapolation from the two component drug programs.

Pharmacokinetic properties

Half-life

Retatrutide ~6 days; cagrilintide ~7-8 days subcutaneous (both support once-weekly dosing).

Routes

subcutaneous

Bioavailability

Both components are lipidated peptides; neither is orally bioavailable. Co-formulation is convenience-driven and does not change individual PK.

Amino-acid sequence

Use & research dosing

No clinical trial of this specific blend exists. Self-experimentation protocols typically maintain each component at its standard schedule: retatrutide 2-12 mg subcutaneous weekly, titrated up over many weeks, and cagrilintide 0.3-2.4 mg subcutaneous weekly, also titrated. Often combined into one weekly injection for convenience. Not FDA-approved; not in any registered trial. Stacking two potent appetite-suppressing mechanisms amplifies GI side-effect risk, so most protocols recommend titrating components individually first.

Research-use framing only. SavePeptides sells nothing for human consumption. Doses above reflect reported research / self-experimentation ranges, not clinical recommendations.

Editorial perspective

Rationale parallels CagriSema, substituting retatrutide for semaglutide. There is no published clinical evidence for this specific combination, so all efficacy expectations are extrapolated from the two individual phase 2/3 programs. Users should titrate each component individually before combining to manage tolerability. Stacking two heavily appetite-suppressing agents raises the risk of severe GI side effects and dehydration. Confidence in safety and efficacy of the blend specifically is low; cite component primaries rather than blend studies.

— SavePeptides editorial desk · last updated 2026-05-25

Cautions & contraindications

Before researching this compound, note:

  • All retatrutide cautions: personal/family history of medullary thyroid carcinoma or MEN2, pancreatitis history, severe gastroparesis, pregnancy
  • All cagrilintide cautions: GI side effects, theoretical pancreatitis risk, injection site reactions
  • Additive and potentially severe GI side effects (nausea, vomiting, constipation) when titrating both simultaneously
  • No human safety data for the specific combination
  • Risk of significant dehydration from compounded vomiting/nausea, with secondary acute kidney injury
  • Lipid panel and resting heart rate changes seen with retatrutide may be additive
  • Hypoglycemia risk if co-administered with insulin or sulfonylureas
  • Identity and concentration of compounded blends from grey-market vendors is unverified

Facts verified

2026-05-25

Confidence

low

What this means

  • limited or absent human clinical data
  • no trials of the specific blend - extrapolation from component drugs

How we check →

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Research-use disclaimer.

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GLP3-R + Cagrilintide Blend · SavePeptides