Compare Peptides

Select any two compounds for a side-by-side comparison of mechanism, uses, risks, and FDA regulatory status.

Popular comparisons

Cagrilintide

AM833, CagriSema (in combination with semaglutide)

Investigational
Metabolic & Weight Management

Tirzepatide

Mounjaro, Zepbound

FDA Approved
GLP-1/GIP Dual Agonist
Overview

A long-acting amylin analog developed by Novo Nordisk. Amylin is a hormone co-secreted with insulin that regulates appetite and gastric emptying. Being developed both standalone and in combination with semaglutide (CagriSema) — a combination showing weight loss exceeding 22% in Phase 3 trials, potentially the next step beyond tirzepatide.

A dual GIP and GLP-1 receptor agonist developed by Eli Lilly. Represents the next generation of incretin-based therapies with potentially superior efficacy to semaglutide for weight loss.

Mechanism of Action

Activates amylin receptors (CALCR/RAMP) in the brain, particularly in the area postrema and hypothalamus, reducing appetite through a pathway distinct from GLP-1. The combination with semaglutide targets two separate appetite-regulating systems simultaneously, producing additive weight loss beyond either agent alone.

Activates both GIP (glucose-dependent insulinotropic polypeptide) and GLP-1 receptors, producing enhanced insulin secretion, appetite suppression, and metabolic improvements beyond what single-agonist drugs achieve.

Common Uses
  • Weight management (investigational)
  • Type 2 diabetes (investigational)
  • Metabolic syndrome
  • Weight management
  • Type 2 diabetes treatment
  • Metabolic health improvement
Known Risks
  • GI side effects (nausea, vomiting) — similar to GLP-1 class
  • Still in Phase 3 trials — full safety profile not established
  • Injection site reactions
  • Long-term effects unknown
  • GI side effects (nausea, diarrhea, vomiting)
  • Pancreatitis risk
  • Injection site reactions
  • Potential thyroid concerns
Regulatory Status
Investigational

Currently in Phase 3 trials as CagriSema (cagrilintide 2.4 mg + semaglutide 2.4 mg). Phase 3 REDEFINE 1 trial showed ~22.7% weight loss at 68 weeks. Potential FDA submission 2026-2027. Represents the next generation beyond tirzepatide in the weight management pipeline.

FDA Approved

FDA-approved as Mounjaro (diabetes, 2022) and Zepbound (weight management, 2023).

This comparison is for educational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional before starting any peptide therapy.