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All Comparisons

Retatrutide vs Liraglutide

Research material comparison: purity standards, available formats, molecular data, batch COA documentation, and regulatory status. For in vitro research use only.

Retatrutide: BLiraglutide: A
AttributeRetatrutideLiraglutide
CategoryMetabolic / Triple AgonistMetabolic / GLP-1 Agonist
Evidence RatingBPhase III / NDA FiledAFDA Approved
Clinical StatusPhase 3 clinical trials (Eli Lilly TRIUMPH program)FDA-approved (Victoza for T2D, Saxenda for obesity)
MechanismRetatrutide simultaneously activates three receptors: GLP-1 (reduces appetite, slows gastric emptying, improves insulin secretion), GIP (enhances insulin sensitivity, glucose control), and glucagon (increases energy expenditure, fat oxidation, thermogenesis). This triple synergy combines reduced cal...Liraglutide binds to GLP-1 receptors on pancreatic β-cells, increasing intracellular cAMP and triggering glucose-dependent insulin secretion. It suppresses glucagon release, slows gastric emptying, and acts on hypothalamic appetite centers to reduce food intake and increase satiety. A fatty acid (C1...
Half-Life~6 days (allows once-weekly dosing)~13 hours
BioavailabilitySC injection~55% SC
Molecular Weight~3,751 g/mol
WADA StatusNot ProhibitedNot Prohibited
Research Half-Life~6 days (allows once-weekly dosing)~13 hours
Key Use Cases
  • Weight Management
  • Metabolic Health
  • Weight Management
  • Metabolic Health
  • Cardiovascular
Safety Concerns
  • GI side effects (dose-related, 13-63% across dose groups): nausea, vomiting, diarrhea, constipation; mostly mild to moderate
  • GI events partially mitigated with lower starting dose (2 mg vs 4 mg initial dose)
  • Dose-dependent heart rate increases peaking at 24 weeks, declining thereafter
  • Common: nausea (39%), diarrhea (21%), constipation (19%), vomiting (15%), headache (13%)
  • GI side effects are dose-dependent and typically diminish over weeks
  • FDA black box warning for thyroid C-cell tumors (rodent data)
Contraindications
  • Not yet established -- product is investigational
  • Likely similar to GLP-1 class: personal/family history of medullary thyroid carcinoma, MEN2 (precautionary)
  • Pregnancy (based on GLP-1 class)
  • Monitoring recommended for muscle mass, bone density, GI motility per GLP-1 class concerns
  • Personal or family history of medullary thyroid carcinoma
  • Multiple endocrine neoplasia syndrome type 2 (MEN2)
  • History of pancreatitis
  • Pregnancy (category X for Saxenda)
Regulatory (US)Not FDA-approved. Phase 3 TRIUMPH program ongoing (Eli Lilly). TRIUMPH-4 reported 28.7% body weight loss at 12 mg over 68 weeks. Seven Phase 3 readouts expected in 2026. Regulatory submission expected 2026; approval anticipated 2027-2028.FDA-approved: Victoza (T2D, 2010), Saxenda (obesity, 2014). Prescription only.

Research Material Specifications

Catalog specifications for the corresponding research materials, including batch documentation coverage.

SpecificationRetatrutideLiraglutide
Purity Standard≥98%
CAS Number2381089-83-2
Molecular FormulaC₂₂₅H₃₄₈N₆₀O₆₈S₂
Available Formats20mg, 10mg
Batch COAs Published2 on file
Stock StatusIn stock

Availability at Volta Peptides

Retatrutide 20mg

≥98% purity · HPLC verified · In stock

$99

Liraglutide

Not currently stocked at Volta Peptides.

Research Disclaimer: This comparison is provided for educational purposes only. All products are sold exclusively for in vitro research use. The information presented is based on published preclinical and clinical research and does not constitute medical advice. Consult a qualified healthcare professional before making any decisions regarding peptide use.

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