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All Comparisons

Retatrutide vs Eloralintide

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

Retatrutide: BEloralintide: C
AttributeRetatrutideEloralintide
CategoryMetabolic / Triple AgonistWeight Loss & Metabolic
Evidence RatingBPhase III / NDA FiledCPhase II Clinical Trials
Clinical StatusPhase 3 clinical trials (Eli Lilly TRIUMPH program)Phase II clinical trials by Eli Lilly. Active development as of 2025.
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...Amylin receptor agonist that promotes satiety and reduces food intake through a pathway distinct from GLP-1 signaling. Amylin is normally co-secreted with insulin from pancreatic beta cells and acts on brain areas controlling appetite.
Half-Life~6 days (allows once-weekly dosing)
BioavailabilitySC injection
Molecular Weight
WADA StatusNot Prohibited
Research Half-Life~6 days (allows once-weekly dosing)
Key Use Cases
  • Weight Management
  • Metabolic Health
  • Weight management
  • Appetite suppression
  • Metabolic research
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
  • Nausea is the most commonly reported adverse effect (consistent with amylin agonist class)
  • Limited long-term safety data available
  • Clinical trial safety monitoring ongoing
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
  • Investigational compound — not available outside clinical trials
  • Pregnancy/breastfeeding
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.Investigational New Drug (IND). Phase II trials ongoing. Not FDA-approved.

Research Material Specifications

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

SpecificationRetatrutideEloralintide
Purity Standard≥98%≥98%
CAS Number2381089-83-2N/A
Molecular FormulaC₂₂₅H₃₄₈N₆₀O₆₈S₂N/A
Available Formats20mg, 10mg, 5mg, 30mg10mg
Batch COAs Published
Stock StatusIn stockOut of stock

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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