Regulatory status
Read this section before ordering. Cagrilintide is an investigational compound. It holds no marketing authorisation from the Medicines and Healthcare products Regulatory Agency in the United Kingdom, from the Food and Drug Administration in the United States, or from the European Medicines Agency.
A regulatory application covering a fixed dose combination containing cagrilintide was submitted to the FDA in December 2025, and a review decision has been anticipated during 2026. Approval of a combination product elsewhere would not make this material a licensed medicine in the United Kingdom, and it would not change the basis on which this listing is supplied. The status of this compound is under periodic review and this page will be updated if it changes.
Under the Human Medicines Regulations 2012 an investigational compound of this kind may not lawfully be supplied for use in humans outside a clinical trial that has been authorised by the MHRA and given a favourable opinion by a research ethics committee.
This listing is an analytical reference standard for laboratory research and nothing else. NH Peptides does not supply it for use in humans or animals, does not supply it to individuals for personal use, and provides no information on this page relating to any such use.
What is cagrilintide?
Cagrilintide is a synthetic long acting analogue of amylin, a peptide hormone produced by the pancreatic beta cells. In the published pharmacology literature it is characterised as an agonist at the amylin and calcitonin receptor family. It carries the development code AM833 and originates from Novo Nordisk.
The designation is a development code rather than an international non-proprietary name, which is normal for a compound that has not completed regulatory review.
Where the evidence stands
The compound has been studied in clinical development, both alone and as part of a fixed dose combination. Trial data are the property of the sponsor and are published in the peer reviewed literature and on trial registries. This page does not summarise those results, discuss any indication under investigation, or restate any endpoint, because doing so would describe a use that this material is not supplied for.
Investigators should work from the primary literature and the trial registry record. A large volume of secondary commentary about this compound is in circulation and much of it is unreliable.
Specification figures for cagrilintide
The sequence, molecular formula and molecular weight for the lot supplied are stated on its certificate of analysis. Published figures for research compounds are not always consistent between sources, so this page defers to the certificate rather than restating a value that may not match the material in the vial.
Working with material of this class
This is a modified peptide carrying a lipid side chain, and its analytical profile is correspondingly more complex than the short unmodified sequences in the catalogue. Related substance peaks are more numerous and a purity figure alone tells you less about a lot than it does for a tripeptide. Read the chromatogram on the certificate rather than the headline figure.
Acylated peptides also behave differently in solution from unmodified ones. They are more prone to aggregation and to surface adsorption, which matters when preparing dilute working solutions.
Analysis and certification
Each lot of cagrilintide is analysed by an independent laboratory using RP-HPLC with LC-MS identity confirmation before it is released for sale. The certificate of analysis is published against the lot number rather than the product page, so the document you read is the document for the vial you receive.
Research use only
NH Peptides supplies cagrilintide as an analytical reference standard for laboratory research. It is not supplied for any use in humans or animals, and no information on this page describes or implies any such use. Sale is restricted to qualified researchers and to purchasers acting on behalf of a research institution, laboratory or business.





