Cagrilintide: research, legal status and who sells it
Cagrilintide is an investigational amylin analogue from Novo Nordisk. It is not approved, and the FDA says it cannot be used in compounding.
By Editorial team. Updated Oct 14, 2026.
Awaiting expert review
This page is information, not medical advice. Cagrilintide is not approved as a medicine in the markets below unless stated. We don't publish dosing or usage instructions.
- Also known as
- CagriSema (combination with semaglutide)
- Category
- Investigational long-acting amylin analogue
- Evidence level
- Late-stage human trials
- Price range
- $2.60/mg to $34.00/mg, median $8.90/mg across 61 vendors (compare)
- Our lab tests
- None yet (how testing will work)
Legal and regulatory status
| Where | Status |
| United States | Not FDA-approved; FDA states that cagrilintide cannot be used in compounding under federal law and is not a component of any FDA-approved drug [1]. |
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| United Kingdom | No UK-licensed medicine containing cagrilintide appears in the MHRA products database [2]. |
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| European Union | No medicine containing cagrilintide is authorized in the EU, according to EMA's central and Article 57 product data [3][4]. |
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| Canada | No product containing cagrilintide appears in Health Canada's Drug Product Database [5]. |
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| Australia | Cagrilintide is not named in Australia's Poisons Standard (October 2026) [6]. |
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| Sport (WADA) | Not named on the 2026 Prohibited List; its section S0 bans any pharmacological substance with no current approval for human therapeutic use [7]. |
Summaries of official sources, checked Oct 14, 2026. Rules change; follow the source links. Not legal advice.
What it is
Cagrilintide is a long-acting analogue of amylin, a pancreatic hormone that promotes satiety [8]. It has been tested on its own and together with semaglutide, a combination known as CagriSema [9].
Research status
In a 26-week phase 2 trial of 706 adults with overweight or obesity, cagrilintide produced 6.0% to 10.8% average weight loss across five doses, compared with 3.0% on placebo; the highest dose also beat the comparator liraglutide (10.8% versus 9.0%) [8]. Nausea was reported by 20% to 47% of people on cagrilintide versus 18% on placebo [8]. In the phase 3 REDEFINE 1 trial, the cagrilintide–semaglutide combination produced 20.4% average weight loss at 68 weeks versus 3.0% on placebo; gastrointestinal adverse events affected about 80% of people on the combination and 40% on placebo [9]. In adults with type 2 diabetes (REDEFINE 2), weight fell 13.7% with the combination versus 3.4% with placebo [10].
Regulatory status
Cagrilintide is not approved in the US, the EU, the UK or Canada [11][3][2][5]. The FDA states that cagrilintide cannot be used in compounding under federal law and is not a component of any FDA-approved drug [1]. It is not named in Australia’s Poisons Standard [6] or on WADA’s 2026 Prohibited List, although WADA’s section S0 bans substances with no current approval for human therapeutic use [7].
Quality and testing considerations
With no approved product anywhere we track, every cagrilintide or “CagriSema” vial sold online is unapproved. The FDA’s general warning applies: unapproved versions of these drugs do not undergo its review for safety, effectiveness or quality [1]. Its warning letters also make clear that a “research use only” label does not change how a product marketed for people is treated [12].
Where it’s sold
No approved cagrilintide product exists; the tables below track unapproved “research” listings and prices.
Cagrilintide prices: cheapest listings
The five lowest $/mg listings out of 93. See all Cagrilintide prices
Prices come from each vendor's public product feed and were last fetched Oct 15, 2026.
They exclude shipping and discounts. $/mg uses the labeled amount, not measured content. A transparency score marked * is based on fewer than six checks; checks we couldn't complete score 0. How we compare prices.
Sources
- FDA's Concerns with Unapproved GLP-1 Drugs Used for Weight Loss (content current as of 1 October 2026). U.S. Food and Drug Administration. Accessed Oct 14, 2026
- MHRA Products: licensed-medicine search for "cagrilintide". Medicines and Healthcare products Regulatory Agency (UK). Accessed Oct 14, 2026
- EMA medicines data: centrally authorised human medicines (export of 14 October 2026). European Medicines Agency. Accessed Oct 14, 2026
- EMA Article 57 product data: medicines authorised in the EU/EEA (data as of 9 October 2026). European Medicines Agency. Accessed Oct 14, 2026
- Drug Product Database online query (searched by active ingredient). Health Canada. Accessed Oct 14, 2026
- Therapeutic Goods (Poisons Standard—October 2026) Instrument 2026 (F2026L01327, registered 30 September 2026). Federal Register of Legislation, Australian Government. Accessed Oct 14, 2026
- World Anti-Doping Code International Standard: Prohibited List 2026 (in force 1 January 2026). World Anti-Doping Agency. Accessed Oct 14, 2026
- Once-weekly cagrilintide for weight management in people with overweight and obesity: a phase 2 trial. The Lancet (2021). Accessed Oct 14, 2026
- Coadministered Cagrilintide and Semaglutide in Adults with Overweight or Obesity (REDEFINE 1). New England Journal of Medicine (2025). Accessed Oct 14, 2026
- Cagrilintide-Semaglutide in Adults with Overweight or Obesity and Type 2 Diabetes (REDEFINE 2). New England Journal of Medicine (2025). Accessed Oct 14, 2026
- Drugs@FDA: FDA-Approved Drugs (database searched by active ingredient). U.S. Food and Drug Administration. Accessed Oct 14, 2026
- Warning Letter to USApeptide.com (MARCS-CMS 696885), 26 February 2025. U.S. Food and Drug Administration. Accessed Oct 14, 2026