Molecular profile
- Class
- Acylated amylin analogue
- Origin / design
- Engineered for prolonged amylin-receptor activity
Peptide research profile
Also known as AM833 · Long-acting amylin analogue
An investigational long-acting amylin analogue studied once weekly for weight management, alone and with semaglutide.
Dosing literacy
Cagrilintide dosing remains investigational. Phase 2 research tested a broad weekly dose range with escalation. This is educational source context—not a protocol or recommendation.
Scaling framework
Lower maintenance arms in the dose-finding study.
Includes the 2.4 mg dose used in combination research.
Highest cagrilintide-only arm in the cited study; not an approved dose.
Schedule literacy
The clinical development program uses weekly administration.
The dose-finding trial included up to six weeks of dose escalation.
CagriSema schedules should not be interpreted as cagrilintide-only evidence.
Multiple doses have direct phase 2 human data, but the compound remains investigational.
Research best practices
Keep cold, dry, and protected from light according to the manufacturer certificate or validated lab SOP.
Use sterile technique, refrigerate as validated, and avoid repeated freeze–thaw cycles.
Record lot, concentration, preparation date, and the identity/purity documentation used by the lab.
Research orientation
These themes describe recurring questions in published research. They are not claims of effectiveness or recommendations for use.
A phase 2 dose-finding trial compared five weekly doses with placebo and liraglutide.
Amylin pathways influence satiation and gastric emptying.
CagriSema studies combine cagrilintide with semaglutide.
Trials use escalation to reach maintenance exposures and manage tolerability.
Evidence map
Study models remain visible so laboratory and animal findings are not mistaken for established human outcomes.
Weekly 0.3, 0.6, 1.2, 2.4, and 4.5 mg arms were studied for 26 weeks.
Cagrilintide 2.4 mg was studied with semaglutide 2.4 mg in type 2 diabetes.
No cagrilintide-only product has an approved public dosing label.
Recorded protocol library
These amount records are independent from vial strength, reconstitution volume and measuring device. A recorded source is not the same as study backing, and these values are not recommendations.
0.3 mg
Sign in for schedule, duration and source context.
2.4 mg
Sign in for schedule, duration and source context.
4.5 mg
Sign in for schedule, duration and source context.
Technical reference
Curated sources