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Legal status · United Kingdom

Is GUBamy legal in the United Kingdom?

Written by Reviewed Sep 2026

Not approvedMetabolicHuman studies cited: 1

Direct answer

No. GUBamy is not approved for any medical use in the United Kingdom; its classification is "Investigational, not licensed". Lawful access is limited to registered clinical trials. "Research use only" labeling on vials sold online does not make human use lawful. On the evidence, 1 human study is cited on its profile.

GUBamy in the United Kingdom at a glance

ClassificationInvestigational, not licensed
MHRA approval statusNot approved by MHRA; investigational
Human studies cited1 of 4 citations on the profile
ReviewedSep 2026

Classification and note come from the GUBamy profile, checked against Medicines and Healthcare products Regulatory Agency (MHRA) listings at the reviewed date.

What this means

  • 01

    GUBamy is being studied in registered clinical trials but has not received MHRA marketing approval in the United Kingdom.

  • 02

    Lawful human access is limited to trial participation or a formal early-access scheme where one exists; there is no pharmacy product to prescribe.

  • 03

    Vials sold online "for research use only" are not trial material, and that label does not make human use lawful.

What GUBamy is

A long-acting amylin analogue from Gubra with one completed phase 1 trial of 76 people sponsored by AbbVie. No result from that trial, and no other human or animal data, has been published; PubMed holds zero records for the compound. Weight loss figures circulating for it could not be traced to any primary source.

GUB014295, referred to as GUBamy in its originator's communications, is a long-acting analogue of amylin, the pancreatic hormone co-secreted with insulin that slows gastric emptying, suppresses glucagon and promotes satiety. It was discovered by the Danish company Gubra.

Mechanism: Amylin acts on receptors formed by the calcitonin receptor paired with receptor activity modifying proteins, in the hindbrain area postrema and elsewhere, to slow gastric emptying, suppress post-meal glucagon secretion and reduce food intake by promoting meal termination. Native amylin aggregates and lasts minutes; long-acting analogues are engineered to resist aggregation and to bind albumin or carry a lipid chain so that they can be dosed weekly.

Regulatory history: Not approved. One completed phase 1 (NCT06144684, 76 participants, sponsor AbbVie) with safety primary outcomes; no results posted, no publications.

How MHRA treats this kind of product

Licenses medicines for the UK market. A compound without a marketing authorisation is an unlicensed medicine, which can only lawfully be supplied for human use through a prescriber under the specials scheme, not sold as a research product.

The classification above is the The Longevity Archive reading of Medicines and Healthcare products Regulatory Agency listings for GUBamy at the reviewed date, not a legal opinion. Rules change, and importing, prescribing and possessing a compound can each be treated differently. Check the regulator directly before acting on anything here.

GUBamy in other countries

Frequently asked questions

Is GUBamy legal in the United Kingdom?

No. GUBamy is not approved for any medical use in the United Kingdom; its classification is "Investigational, not licensed". Lawful access is limited to registered clinical trials. "Research use only" labeling on vials sold online does not make human use lawful. On the evidence, 1 human study is cited on its profile.

Can I buy GUBamy in the United Kingdom?

No approved product exists to buy. In the United Kingdom GUBamy is classified as "Investigational, not licensed", so there is no licensed pharmacy product. Vendors selling it "for research use only" are not selling it for human use, and that label does not change its legal status. This site does not list or recommend vendors.

Is GUBamy MHRA approved?

No. In the United Kingdom GUBamy is classified as "Investigational, not licensed", which is not a MHRA marketing approval. For comparison, the US FDA status is: Not approved. One completed phase 1 (NCT06144684, 76 participants, sponsor AbbVie) with safety primary outcomes; no results posted, no publications.. On the evidence, 1 human study is cited on its profile.

Related compounds in the United Kingdom

Full research profile

Mechanism, cited studies, FDA status and the full legal summary for GUBamy live on its compound profile.

GUBamy profile

This page is general information about the regulatory status of GUBamy in the United Kingdom, current as of Sep 2026. It is not legal advice, and classifications change; check Medicines and Healthcare products Regulatory Agency directly or consult a lawyer for a specific situation. Educational use only. This database summarizes published research. It is not medical advice and contains no dosing protocols or recommendations for personal use. The Longevity Archive has no vendor relationships and does not recommend where to buy anything.