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Metabolic & Weight Management

Cagrilintide + Semaglutide calculator

The investigational fixed combination of the amylin analog cagrilintide with the GLP-1 agonist semaglutide, developed for greater weight loss.

Also known as: CagriSema, Amylin + GLP-1 combination

FDA status — not an approved drug Not FDA-approved. CagriSema (cagrilintide with semaglutide) is an investigational combination in clinical development and has not been approved.

48 units
on a 100-unit syringe
0.48 mL
volume drawn
5 mg/mL
concentration
4 doses
per vial
050100

Schedule Cagrilintide + Semaglutide → Set your dosing schedule and get a phone notification when each dose is due. Free.

A worked example

A 10 mg vial reconstituted with 2 mL of bacteriostatic water gives 5 mg/mL. A 2400 mcg dose is then 0.48 mL — about 48 units on a 100-unit insulin syringe, giving roughly 4 doses per vial before accounting for residual volume left in the vial and syringe.

Prefer paper? Download the printable Cagrilintide + Semaglutide dosing chart (PDF) — every vial size and water volume in syringe units, with the same review byline as this page. All charts →

Commonly cited dose range

Figures circulating for Cagrilintide + Semaglutide run from 2400 mcg to 2400 mcg. The combination is dosed once weekly after titration, with each component at a fixed amount. Figures reflect published phase 3 dosing. This is investigational data, not a prescribing guide.

Read this as reference information, not instruction. These numbers describe what is commonly discussed, not what is right for any individual. Dose, frequency, and whether to use Cagrilintide + Semaglutide at all are decisions for a licensed clinician who knows your history.

Common questions

What is CagriSema?

CagriSema is the development name for a fixed combination of cagrilintide (an amylin analog) and semaglutide (a GLP-1 agonist) in a single once-weekly injection, designed to produce more weight loss than either alone.

Is CagriSema approved?

No. It is an investigational combination that has completed phase 3 studies but has not been approved.

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