Cagrilintide

Cagrilintide (NN9838, formerly known as AM833) is a long-acting amylin analog developed by Novo Nordisk for the treatment of obesity. It is a synthetic peptide that mimics the effects of amylin, a hormone co-secreted with insulin from pancreatic beta cells that plays a role in glucose homeostasis and appetite regulation. Cagrilintide works by activating amylin […]

Normal Protocol

Advanced Protocol

Overview

Also Known As

NN9838, AM833, CagriSema component

Mechanism of Action

Activates amylin receptors (AMY1, AMY2, AMY3) in the area postrema and nucleus tractus solitarius to promote satiety and reduce food intake. Slows gastric emptying, suppresses postprandial glucagon secretion, and modulates glucose homeostasis. Long-acting due to fatty acid acylation enabling albumin binding.

Product

NN9838, AM833, CagriSema component vial
Dosing & Administration
Typical protocols and routes

Half-Life

Approximately 160 hours (once-weekly dosing), achieved through C18 fatty diacid acylation enabling reversible albumin binding.

Administration Routes

subcutaneous

Dosing Protocols

Provider protocol: 10mg vial reconstituted with 2mL bacteriostatic water; 10 units (0.1mL = 0.5mg) daily subcutaneous injection, vial lasts 20 days (normal dose). Advanced: 10mg vial with 1mL bacteriostatic water; 10 units (0.1mL = 1mg) daily, vial lasts 10 days. Clinical trials: 1.2mg to 4.5mg once weekly subcutaneous injection.
Research
Key findings and status

Key Research Findings

Phase 2 trials showed dose-dependent weight loss up to 10.8% at 26 weeks. CagriSema (cagrilintide + semaglutide) Phase 3 REDEFINE trials demonstrated up to 22.7% body weight reduction. Novo Nordisk development program ongoing for obesity and type 2 diabetes indications.
Detailed Information

Cagrilintide (NN9838, formerly known as AM833) is a long-acting amylin analog developed by Novo Nordisk for the treatment of obesity. It is a synthetic peptide that mimics the effects of amylin, a hormone co-secreted with insulin from pancreatic beta cells that plays a role in glucose homeostasis and appetite regulation.

Cagrilintide works by activating amylin receptors in the brain, particularly in the area postrema and nucleus tractus solitarius, to promote satiety and reduce food intake. It slows gastric emptying and suppresses postprandial glucagon secretion, contributing to improved glycemic control and weight management.

In clinical trials, cagrilintide has been studied both as a standalone treatment and in combination with semaglutide (the combination known as CagriSema). Phase 2 and Phase 3 trials have demonstrated significant weight loss — with the CagriSema combination showing up to 15-25% body weight reduction in some studies, exceeding results seen with either drug alone.

Cagrilintide is administered as a once-weekly subcutaneous injection due to its engineered long half-life achieved through fatty acid acylation, similar to the design approach used for semaglutide and liraglutide.

Safety & Legal

Side Effects & Warnings

Most common: nausea, diarrhea, vomiting, constipation (generally mild to moderate, transient). Injection site reactions reported. Similar GI side effect profile to other incretin and amylin-based therapies. Dose escalation helps mitigate GI tolerability.

Legal Status

Investigational — not yet FDA approved. Available as research peptide.
Molecular Data
Chemical properties

Molecular Weight

Approximately 3950 g/mol

Amino Acid Sequence

Modified human amylin analog with amino acid substitutions and C18 fatty diacid acylation at Lys position for extended half-life.

Quick Facts

Class

Amylin Analog

Research Status

Clinical Trials

Half-Life

Approximately 160 hours (once-weekly dosing), achieved through C18 fatty diacid acylation enabling reversible albumin binding.

Routes

subcutaneous

Category

GLP-1 Agonists