Compare Peptides

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

Popular comparisons

Orforglipron

LY3502970, Eli Lilly oral GLP-1

Investigational
GLP-1 Agonist

Tirzepatide

Mounjaro, Zepbound

FDA Approved
GLP-1/GIP Dual Agonist
Overview

A non-peptide, small-molecule GLP-1 receptor agonist developed by Eli Lilly. Unlike semaglutide and tirzepatide which are peptides requiring injection, orforglipron is a fully oral pill taken once daily with no fasting requirement. Phase 3 trials are underway, potentially making it the first truly convenient oral GLP-1 option.

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 GLP-1 receptors through a non-peptide chemical scaffold, producing the same downstream effects as injectable GLP-1 agonists — appetite suppression, insulin secretion, and slowed gastric emptying. The oral bioavailability is achieved through its small-molecule structure, unlike oral semaglutide (Rybelsus) which requires strict fasting protocols.

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 health improvement
  • Weight management
  • Type 2 diabetes treatment
  • Metabolic health improvement
Known Risks
  • GI side effects (nausea, diarrhea, vomiting) — similar to injectable GLP-1s
  • Still in Phase 3 trials — full safety profile not established
  • Long-term cardiovascular outcomes data not yet available
  • Not yet approved for any indication
  • GI side effects (nausea, diarrhea, vomiting)
  • Pancreatitis risk
  • Injection site reactions
  • Potential thyroid concerns
Regulatory Status
Investigational

Currently in Phase 3 clinical trials for obesity and type 2 diabetes. Phase 2 results showed ~14.7% weight loss at 36 weeks — comparable to injectable semaglutide. If approved, would be the first non-peptide oral GLP-1 agonist, removing the injection barrier for many patients. Potential approval 2026-2027.

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.