Cagrilintide
Long-acting amylin analogue · sold as “Amylix”
Investigational long-acting amylin analogue studied alone and combined with semaglutide (CagriSema).
Not FDA-approved. Investigational (Novo Nordisk). CagriSema regulatory submission reported; not approved at last review. This page describes research and public discussion; it is not a recommendation to use.
Overview
Cagrilintide mimics amylin, a hormone co-released with insulin that promotes fullness. Brochure product “Amylix” is described as amylin-based; we profile cagrilintide as the leading clinical amylin analogue. Confirm the actual molecule with any supplier.
Mechanism of action
Agonist at amylin and calcitonin receptors in the brainstem and hypothalamus, increasing satiety and slowing gastric emptying.
Benefits & evidence ratings
Dosing
Doses show what has been studied or discussed — not guidance. Always follow your prescriber.
| Source | Dose | Frequency | Duration | Route |
|---|---|---|---|---|
Phase 2 dose-finding (Lancet 2021) B Human clinical data | 0.3–4.5 mg | Once weekly | 26 weeks | Subcutaneous |
REDEFINE 1 (with semaglutide 2.4 mg) B Human clinical data | 2.4 mg | Once weekly | 68 weeks | Subcutaneous |
Clinical trials & studies
- Phase 22021Once-weekly cagrilintide for weight management (Lancet)
Phase 2; dose-dependent weight loss up to 10.8%.
- Phase 32025Cagrilintide–Semaglutide in Adults with Overweight or Obesity (REDEFINE 1, NEJM)
Mean −20.4% vs −3.0% placebo.
Safety
Side effects
- Nausea, constipation, diarrhea
- Fatigue
- Injection-site reactions
Contraindications
- Pregnancy
- Gastroparesis (theoretical, slows emptying)
Interactions
- Insulin — hypoglycemia risk (pramlintide class warning)
- Additive GI effects with GLP-1 agonists
Long-term safety
Limited to trial durations (~68 weeks).
Regulatory status
Investigational
Investigational (Novo Nordisk). CagriSema regulatory submission reported; not approved at last review.
FAQ
Commonly discussed alongside
Listing a combination does not mean it has been studied or is safe.
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