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All Comparisons

Hexarelin vs Tesamorelin

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

Hexarelin: CTesamorelin: A
AttributeHexarelinTesamorelin
CategoryGrowth Hormone SecretagogueGrowth Hormone Secretagogue
Evidence RatingCPhase I–II Clinical TrialsAFDA Approved
Clinical StatusPhase II completed. Development discontinued due to tolerance/desensitization concerns.FDA-approved (Egrifta SV 2019, Egrifta WR March 2025) for HIV-associated lipodystrophy
MechanismHexarelin binds to and activates the ghrelin/growth hormone secretagogue receptor (GHS-R1a) in the pituitary and hypothalamus through a triple mechanism: direct stimulation of pituitary somatotroph cells to release stored GH, stimulation of hypothalamic GHRH-releasing neurons, and suppression of som...Tesamorelin binds to and stimulates human GRF (growth hormone-releasing factor) receptors on the anterior pituitary with similar potency as endogenous GRF, stimulating synthesis and release of endogenous growth hormone. This increases IGF-1 and IGFBP-3 levels, leading to increased lipolysis and redu...
Half-Life~70 minutes~26–38 minutes
Bioavailability
Molecular Weight~887 g/mol~5135.9 g/mol
WADA StatusProhibitedProhibited
Research Half-Life~70 minutes~26–38 minutes
Key Use Cases
  • Body Composition
  • Anti-Aging
  • Body Composition
Safety Concerns
  • Generally well-tolerated in clinical trials
  • Transient cortisol and prolactin elevation at higher doses
  • Hunger increase (ghrelin receptor activation)
  • Common: injection site reactions (17%), arthralgia (13%), myalgia (6%), peripheral edema (6%)
  • Headache, nausea, and flu-like symptoms reported
  • May increase blood glucose -- monitoring recommended in diabetics
Contraindications
  • Active cancer (GH/IGF-1 axis stimulation)
  • Pituitary tumors
  • Pregnancy and breastfeeding
  • Diabetic retinopathy (GH may worsen)
  • Pregnancy (Category X -- absolute contraindication)
  • Active cancer or history of any tumor (benign or malignant)
  • Pituitary gland disorder, tumor, or history of pituitary surgery
  • History of head injury or radiation treatment to the head
Regulatory (US)Not FDA-approved. Development discontinued. Research chemical only.FDA-approved: Egrifta SV (Oct 2019) and Egrifta WR (March 2025) for HIV-associated lipodystrophy. Prescription only.

Research Material Specifications

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

SpecificationHexarelinTesamorelin
Purity Standard≥98%≥98%
CAS Number140703-51-1218949-48-5
Molecular FormulaN/AC₂₂₃H₃₇₀N₇₂O₆₉S
Available Formats5mg10mg, 20mg, 10mg
Batch COAs Published1 on file
Stock StatusOut of stockIn 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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