Research Database›Metabolic›Cagrilintide
Physician PracticeResearch Use OnlyWADA Prohibited

Cagrilintide

Long-acting amylin analog in Phase III clinical development. Studied for obesity management, particularly in the CagriSema combination with sema. Slow titration required for GI tolerability.

MetabolicWeight ManagementAmylin AnalogInjectablePhase III
QUICK FACTS
CLASSLong-acting amylin analog
MECHANISMAmylin receptor agonism — satiety, gastric emptying, GCG suppression
DEVELOPMENTPhase III — CagriSema combination program
EVIDENCE STATUSInvestigational — Phase II/III data developing
WADA STATUSProhibited
Overview

Cagrilintide is a long-acting synthetic amylin analog developed by Novo Nordisk for obesity management. Amylin is a peptide hormone co-secreted with insulin that regulates satiety, gastric emptying, and GCG secretion. Cagrilintide is designed for once-weekly subcutaneous dosing.

The rationale for combining amylin agonism with GLP-1 agonism is mechanistic complementarity. The CagriSema combination (cagrilintide + sema) is in Phase III development and has shown promising preliminary data suggesting enhanced outcomes versus either agent alone.

Physician practice use involves slow titration from 0.1 mg weekly up to 1–1.5 mg weekly over months. The cumulative GI burden of combining amylin agonism with GLP-class agents requires careful assessment and ongoing monitoring.

Research Areas
Obesity management researchAmylin pathway researchSatiety mechanism researchGLP combination researchWeight management pharmacologyMetabolic hormone research
Available Evidence3 categories
Human (Phase II/III)Phase II shows dose-dependent weight loss. CagriSema combination Phase III program ongoing with preliminary data suggesting enhanced outcomes vs monotherapy.
MechanisticAmylin receptor agonism complements GLP-1 mechanisms through different satiety pathways, potentially additive effects when combined.
UncertainOptimal combination protocols, long-term safety, and definitive Phase III outcomes pending. Not approved.
Documented Research Benefits6 documented
Weight reduction
Phase II human data
Satiety enhancement
amylin mechanism
Gastric emptying modulation
amylin mechanism
GCG suppression
human
GLP-1 complementary pathway
mechanistic
Additive GLP effects
Phase II combination data
Research Pairings3 common
Tirze
GIP/GLP-1 + amylin approach. Cumulative GI burden is the critical consideration in combination.
View Tirze →
Reta
Triple agonist alternative to tirze in combination discussions.
View Reta →
MOTS-c
Metabolic support in combination protocols — physician practice context.
View MOTS-c →

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Safety & Regulatory Status

Cagrilintide is not approved for any indication. GI adverse effects are the primary concern, especially in combination with GLP agents. WADA-prohibited. Research use only. All information for educational reference only.

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