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Understand the source comparison

Growth Hormone Secretagogues Ranked: Clinical Evidence Comparison

The following table ranks growth hormone secretagogues by receptor selectivity, half-life, bioavailability, and documented IGF-1 response based on peer-reviewed clinical trial data. The 'Professional Assessment' column reflects research application suitability

No winner is assigned.

This page preserves a source comparison for education. It does not add a rating, recommendation or clinical judgment.

  • The following table ranks growth hormone secretagogues by receptor selectivity, half-life, bioavailability, and documented IGF-1 response based on peer-reviewed clinical trial data. The 'Professional Assessment' column reflects research application suitability rather than therapeutic recommendation.
  • Ipamorelin
  • Selective GHS-R1a agonist
  • 2 hours
  • 40–60% at 200mcg
  • Minimal cortisol/prolactin elevation
  • Highest selectivity for isolated GH research; requires 2–3× daily dosing
  • MK 677
  • Oral ghrelin mimetic
  • 4–6 hours
  • 60–97% at 25mg daily
  • GHS-R1a with appetite stimulation
  • Only orally bioavailable option; once-daily dosing; appetite confound in 40–60%
  • CJC-1295 with DAC
  • GHRH analog + albumin binding
  • 6–8 days
  • 60–80% sustained
  • GHRH receptor selective
  • Longest half-life; once-weekly protocol; blunted GH peaks vs pulsatile pattern
  • CJC-1295 NO DAC
  • Modified GRF(1-29)
  • 30–60 minutes
  • 30–50% (synergistic with GHRP)
  • Best for timed-pulse studies; pairs with ipamorelin for dual-axis stimulation
  • Tesamorelin
  • GHRH analog (trans-3-hexenoic acid)
  • 38 minutes
  • 45–70%
  • GHRH receptor; visceral fat reduction
  • Only FDA-approved GHS for metabolic indication; daily dosing required
  • GHRP-2
  • Non-selective ghrelin agonist
  • 20–30 minutes
  • 50–80%
  • Elevates cortisol 25–35%, prolactin 15–25%
  • Higher GH amplitude but hormonal confounds limit research utility
  • GHRP-6
  • 40–70%
  • Cortisol/prolactin elevation + appetite
  • Strong appetite stimulation; less selective than ipamorelin
  • Hexarelin
  • Potent ghrelin agonist
  • 70 minutes
  • 100–140% (highest peak)
  • Cardiac receptor density risk at sustained dose
  • Highest GH peak but off-target myocardial effects documented
  • Sermorelin
  • Native GHRH(1-29) analog
  • 8–12 minutes
  • 30–50%
  • Shortest half-life; requires frequent dosing; lowest cost per dose