Can I get it?
Not yet, and not from anyone in the EU. CagriSema is still being studied; it has no marketing authorisation, so it cannot legally be prescribed or dispensed here outside a clinical trial. That is the law, not a limitation of any one clinic.What can I take instead?
Semaglutide is approved in the EU, has published peer-reviewed trial results, and can be prescribed today if a doctor decides it suits a case. It has been authorised in the EU since 6 January 2022.Semaglutide (Wegovy / Ozempic)
Weekly GLP-1 receptor agonist. A doctor may prescribe it if BMI and history match the indications. Requires follow-up.
Tirzepatide (Mounjaro)
Dual GLP-1/GIP agonist. Assessed by the doctor based on comorbidities and BMI.
Liraglutide (Saxenda)
Daily GLP-1 agonist. Indicated in selected patients with elevated BMI after medical evaluation.
Orlistat 120mg
Fat-absorption inhibitor. A non-GLP-1 alternative a doctor may consider based on history.
Rybelsus (oral semaglutide)
A once-daily semaglutide tablet authorised for type 2 diabetes. Any use in weight management is an individual medical decision and may be off-label.
How CagriSema works
Semaglutide activates GLP-1 receptors in the hypothalamic arcuate nucleus and the brainstem area postrema, reducing appetite and slowing gastric emptying. Cagrilintide acts as a dual amylin and calcitonin receptor agonist (DACRA). To lower body weight it requires the presence of the amylin 1 and amylin 3 receptor subtypes (AMY₁R and AMY₃R), which are formed when the calcitonin receptor dimerises with receptor activity-modifying proteins RAMP1 and RAMP3. This amylin-signalling axis is independent of the GLP-1 pathway, which is why a combination of the two can produce additive weight loss (eBioMedicine 2025; Pharmacol Ther 2023).What the studies reported
Every trial behind CagriSema is listed here with its registry number and whether the results are peer-reviewed or a company announcement. Results are grouped by source and evidence grade so journal data and manufacturer announcements cannot be confused.REDEFINE 1 — NCT05567796
REDEFINE 1 — NCT05567796
Randomised, double-blind, placebo-controlled phase 3 trial comparing CagriSema, cagrilintide alone, semaglutide alone, and placebo in adults with obesity or overweight with at least one comorbidity. Published in the New England Journal of Medicine. ClinicalTrials.gov record: NCT05567796.
REDEFINE 2 — NCT05394519
REDEFINE 2 — NCT05394519
Randomised, double-blind, placebo-controlled phase 3 trial in adults with type 2 diabetes and overweight or obesity, testing CagriSema against placebo on top of diet and exercise. Published in the New England Journal of Medicine. ClinicalTrials.gov record: NCT05394519.
FDA filing
FDA filing
Novo Nordisk filed for FDA approval of CagriSema on 18 December 2025. No corresponding EU filing has resulted in a marketing authorisation.
Every NCT identifier links to its ClinicalTrials.gov record. A trial readout is not the same as a peer-reviewed publication.
A note on comparing to semaglutide
Semaglutide’s own weight-loss evidence, from its STEP 1 trial, measured mean change with the 2.4 mg once-weekly dose at 68 weeks; the placebo arm’s mean change was −2.4%. This is a separate trial from CagriSema’s REDEFINE studies, not a direct comparison — results for CagriSema may come from a different dose, duration and patient group.How Hi-Doctor handles it
The product is the online doctor consultation. A licensed doctor decides case by case, and treatment — and a prescription — follow only if the doctor approves. Renewals are reviewed by the same doctor, with ongoing care available for as long as a plan is active. Medication, if prescribed, is paid separately at the pharmacy — Hi-Doctor does not sell medications. See pricing for what the consultation covers.Related reading
- Semaglutide (Ozempic) — evidence and regulatory status
- Liraglutide (Victoza) — evidence and side effects
- Safety and eligibility
- How Hi-Doctor works
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Weight-loss consultation
Answer the weight-loss questionnaire and a registered doctor reviews it.
They decide whether treatment is appropriate, which one, and at what dose —
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