Cotadutide vs HM15211

Head-to-head comparison of Cotadutide (MEDI0382, long-acting GLP-1 and glucagon receptor dual agonist) and HM15211 (HM15211, glucagon-like peptide-1/glucose-dependent insulinotropic polypeptide/glucagon receptor triagonist) — benefits, dosing, side effects, research data, and where to buy.

Research Score

PropertyCotadutideHM15211
CategoryWeight ManagementWeight Management
Full NameMEDI0382, long-acting GLP-1 and glucagon receptor dual agonistHM15211, glucagon-like peptide-1/glucose-dependent insulinotropic polypeptide/glucagon receptor triagonist
Molecular Weight~4,700 DaN/A
Half-LifeApproximately 24 hoursApproximately 1 week
Amino Acids37N/A
Typical Dose0.3-3 mg daily in clinical studiesInvestigational; no established human dose
RouteSubcutaneousSubcutaneous
Purity≥98%≥98%
Studies Count1812
Research StatusClinicalClinical

Cotadutide Benefits

  • body-weight reduction
  • improved insulin sensitivity
  • reduced hepatic fat
  • appetite suppression

HM15211 Benefits

  • appetite suppression
  • greater fat oxidation
  • weight loss
  • improved metabolic markers

Cotadutide Dosing

Once-daily SC in trials|Start low and titrate based on tolerance|Monitor GI adverse effects

HM15211 Dosing

once-weekly subcutaneous injection|titration to effect|maintenance at tolerated dose

Cotadutide Side Effects

  • nausea
  • vomiting
  • diarrhea

HM15211 Side Effects

  • nausea
  • vomiting
  • reduced appetite

Research Overview

Cotadutide

Phase 2 studies reported dose-dependent weight loss and favorable changes in glycemic and liver-related markers. It is one of the most cited synthetic dual-agonist peptides for obesity research.

HM15211

Research has shown potent weight-reducing and metabolic effects in preclinical and translational studies. The compound is being developed as a next-generation incretin-based therapy.

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Common Stacking Partners

Cotadutide stacks with:

dietary-calorie-restrictionexercise-program

HM15211 stacks with:

metformintopiramate
GLP-1glucagon-coagonistdual-agonistobesity-researchglp1gipglucagontriagonistobesity