Peptika.
Cat. 06
Type I · Lyophilised
PK-2026-CAGRIL
Peptika Cagrilintide vial
Lot-tracedEU pharmacyCold-chain 2–8 °C
06 · Weight Management

Cagrilintide.

Long-acting amylin analogue — satiety regulation, often stacked with GLP-1.

Select strengthPer-vial price
Quantity
1
Total
€120.00· 1 vial
Combination presets

Pre-compounded multi-peptide vials. An EU-licensed physician reviews the blend and dosing — anything they decline is refunded.

Build your bag, then either book a consultation (an EU-licensed physician reviews your file — anything declined is refunded) or upload an existing Rx at checkout.

  • Magistral preparation — Directive 2001/83/EC Art. 5(1).
  • Patient-named prescription only — dispensed against a valid Rx.
  • EU-GMP Annex 1 Grade A/B cleanroom compounding.
  • Cold-chain shipping across EU/EEA — 2–5 working days.
Overview

About Cagrilintide.

Cagrilintide is a long-acting analogue of amylin, a pancreatic hormone co-secreted with insulin that signals satiety. Its profile makes it complementary to GLP-1 agonists — the combination (e.g. CagriSema, Cagrilintide + Semaglutide) is in Phase 3 for obesity with promising early data.

Cagrilintide is mostly studied as part of a stacked protocol rather than as a stand-alone weight intervention.

Mechanism of action

Cagrilintide activates amylin receptors (AMY1, AMY2, AMY3) in the area postrema and other CNS sites. Activation slows gastric emptying, reduces glucagon secretion and produces a satiety signal independent of GLP-1.

Posology · for information only

Subcutaneous injection, once weekly. Typical doses range from 0.6 to 2.4 mg. Frequently administered together with Semaglutide on the same day.

Your physician sets the prescription. This is descriptive information, not a self-administration guide.

Storage

Lyophilised: store at 2–8 °C, protect from light. Once reconstituted: 2–8 °C, use within 30 days. Do not freeze.

Evidence baseClinical RCT evidence
Indications studied
Weight management (combination protocols)Satiety regulation
Identification & specifications
INN / Name
Cagrilintide
Form
Lyophilised vial · subcutaneous injection
Strength
5mg vial
Manufacturing
EU-GMP Annex 1 · Grade A/B
Endotoxins
European Pharmacopoeia 2.6.14 · LAL assay
Identity & purity
HPLC + MS · > 98%
Cold chain
Validated 2–8 °C, monitored end-to-end
Regulatory basis
Directive 2001/83/EC · Article 5(1)
Logistics

2–5 working days

EU / EEA cold-chain delivery, 2–8 °C monitored end-to-end with digital temperature log. Tracking link sent on dispatch.

Legal status

Magistral preparation

Patient-named preparation under Directive 2001/83/EC Article 5(1). Dispensed exclusively against a valid EU prescription.

Cross-border

EU prescription recognition

Prescriptions written in one EU member state are recognised in others under Directive 2011/24/EU on cross-border healthcare.