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Encyclopedia entry

Ipamorelin

Evidence: Mixed evidence
OM

Oliver Mackman · Editorial director · Best Business Loans Ltd (16833937)

Last updated 2026-06-03

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AI-friendly summary · Ipamorelin

Ipamorelin is a synthetic pentapeptide and selective growth-hormone secretagogue originally developed by Novo Nordisk in the late 1990s. Unusually for a research peptide it reached phase II human trials in postoperative ileus before development was discontinued for failing endpoints. It holds no marketing authorisation in any country and is sold in the UK only as a research chemical.

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Ipamorelin: a synthetic pentapeptide that stimulates pituitary release of endogenous growth hormone. Originally developed by Novo Nordisk. Phase II discontinued. No marketing authorisation in any country.

Mechanism of action

How Ipamorelin works

Ipamorelin is a selective agonist of the ghrelin receptor (GHSR-1a) on pituitary somatotrophs. Binding triggers a calcium-mediated release of stored growth hormone in a pulsatile pattern that approximates physiological GH secretion. Selectivity is the design feature: unlike older GH secretagogues, ipamorelin does not meaningfully stimulate cortisol or prolactin release in published preclinical work.

Source: Raun K et al. European Journal of Endocrinology, 1998 (original characterisation)

Pharmaceutical development history

Ipamorelin is one of the few research peptides with documented phase II human safety data. Novo Nordisk discovered the compound in the late 1990s. Helsinn licensed the postoperative ileus programme in the 2000s and ran the phase II trial. Endpoints were not met and the programme was discontinued. No pharmaceutical sponsor has since pursued a registration filing in any indication.

Why this entry exists

Ipamorelin is unusual because it has phase II human safety data, unlike most research peptides. That does not make it a medicine. It was tested for a specific indication (postoperative ileus) and failed. Any present-day human use is off-label and unsupervised. We do not publish dosing or protocols. The encyclopedia entry exists to give readers access to the regulatory and pharmaceutical history they will not find on retailer pages.

UK regulatory status

Risks and unknowns

What the literature does not yet show about Ipamorelin

Known concerns

Open questions in the literature

Regulatory note

Not controlled under UK law. No UK marketing authorisation. Sold legally as a research chemical when marketed without therapeutic claims. WADA prohibited list S2 peptide hormones class. Becomes an unlicensed medicinal product the moment a retailer or commentator makes therapeutic claims about it.

Important: PeptideClear publishes encyclopedia commentary only and does not recommend human use. Speak to a UK-registered prescriber before any medical decision.

Editorial

Baseline panels to track

If you are working with a UK private doctor or NHS prescriber on a peptide protocol, these are the blood panels typically ordered at baseline for Ipamorelin. Not a recommendation for self-administered testing.

  • IGF-1. Downstream marker of growth hormone activity. Prescribers track baseline and post-administration response on any GH-secretagogue protocol.
  • Prolactin. Selectivity is the design feature of ipamorelin: unlike older GH secretagogues, it does not meaningfully stimulate prolactin release in preclinical work. Baseline plus follow-up prolactin tests that selectivity in practice.
  • HbA1c. 90-day glucose average. GH-secretagogue stimulation can shift glucose metabolism over a longer time window, and HbA1c captures it.

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Frequently asked questions

Is ipamorelin legal in the UK?
Ipamorelin is not controlled under the Misuse of Drugs Act 1971 and is not scheduled under the Psychoactive Substances Act 2016. It is sold by UK research peptide retailers under "research use only, not for human or animal consumption" framing. It holds no UK marketing authorisation.
What does the human evidence show for ipamorelin?
Ipamorelin progressed to phase II human trials for postoperative ileus in the 2000s under Helsinn licensee development of the original Novo Nordisk programme. The phase II endpoints were not met and pharmaceutical development was discontinued. No human RCT has demonstrated efficacy in any approved indication, and no phase III data exists.
What is the regulatory status of ipamorelin?
Ipamorelin holds zero marketing authorisations in any country. Its UK regulatory tier is the same as other unlicensed research peptides: legal to sell as a research chemical without health claims, an unlicensed medicinal product the moment therapeutic claims are attached. It is on the WADA prohibited list (S2 peptide hormones class).
What forms is ipamorelin available in?
UK research peptide retailers list ipamorelin most commonly as lyophilised powder in 2mg or 5mg vials for reconstitution. PeptideClear publishes no dosing or human-use instructions; this is encyclopedia commentary only.
Where can I learn more about ipamorelin?
A PubMed search for "ipamorelin" returns roughly 60 papers, including the original Novo Nordisk characterisation by Raun et al. in 1998 and the phase II trial reports from the Helsinn programme. The "Pharmaceutical development history" section above summarises the development arc.

Where to buy Ipamorelin in the UK

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Clinical evidence record

Read the clinical evidence record for Ipamorelin

Top peer-reviewed citations, mechanism of action, structured UK regulatory status. Machine-readable companion to this encyclopedia entry.

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Reviewed by Oliver Mackman, editorial director · last reviewed 2026-06-03T12:00:00.000Z
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