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Source comparison

Tesamorelin Protocol: Clinical Comparison

Tesamorelin GHRH analogue—stimulates pituitary GH release while preserving feedback loops 2mg SC daily (evening) 15–22% +60–90 ng/mL (moderate, physiological) Low—transient hyperglycemia in first month, improves with VAT reduction Gold standard for visceral fa

This comparison does not assign a generated winner or score.

  • Tesamorelin
  • GHRH analogue—stimulates pituitary GH release while preserving feedback loops
  • 2mg SC daily (evening)
  • 15–22%
  • +60–90 ng/mL (moderate, physiological)
  • Low—transient hyperglycemia in first month, improves with VAT reduction
  • Gold standard for visceral fat targeting in metabolic optimization; requires daily injections but avoids supraphysiological GH spikes
  • Ipamorelin
  • Ghrelin mimetic—stimulates GH via ghrelin receptor, no cortisol/prolactin elevation
  • 200–300 mcg SC 2–3× daily
  • 8–12% (less selective for VAT)
  • +40–60 ng/mL (lower peak)
  • Very low
  • Better tolerated but less effective for pure VAT reduction; useful when tesamorelin causes persistent injection site reactions
  • CJC-1295 (with DAC)
  • Long-acting GHRH analogue—extends GH elevation for 7–10 days per injection
  • 2mg SC weekly
  • 10–15% (comparable to tesamorelin at 6 months)
  • +70–110 ng/mL (higher, sustained)
  • Moderate—prolonged IGF-1 elevation increases insulin resistance risk
  • Less physiological pulsatility; convenient dosing but higher risk of IGF-1 overshooting therapeutic range
  • Exogenous GH (somatropin)
  • Direct GH replacement—bypasses endogenous regulation entirely
  • 0.2–0.4 IU SC daily
  • 18–25% (most potent)
  • +120–200 ng/mL (supraphysiological)
  • High—dose-dependent insulin resistance, fluid retention, joint pain
  • Most effective for VAT reduction but least physiological; reserved for confirmed GH deficiency (IGF-1 <100 ng/mL)
  • Sermorelin
  • Short-acting GHRH analogue—stimulates pituitary but clears rapidly
  • 200–500 mcg SC daily
  • 6–10% (weakest VAT effect)
  • +30–50 ng/mL (minimal)
  • Mildest option; used in patients with mild metabolic dysfunction or as adjunct to other interventions
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