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Source comparison

MK-677 for IGF-1 Elevation Research: Clinical Evidence Comparison

MK-677 25mg Ghrelin receptor agonist 2–3× baseline 60–127% above baseline Yes. Maintains circadian rhythm Once daily Gold standard for sustained IGF-1 research. No tolerance development, oral administration, preserved endogenous secretion patterns GHRP-2 100mc

This comparison does not assign a generated winner or score.

  • MK-677 25mg
  • Ghrelin receptor agonist
  • 2–3× baseline
  • 60–127% above baseline
  • Yes. Maintains circadian rhythm
  • Once daily
  • Gold standard for sustained IGF-1 research. No tolerance development, oral administration, preserved endogenous secretion patterns
  • GHRP-2 100mcg
  • Growth hormone releasing peptide
  • 5–8× baseline (acute spike)
  • 20–35% above baseline
  • No. Blunts natural pulses
  • 2–3× daily subcutaneous
  • Strong acute response but rapid desensitization. IGF-1 elevation declines significantly after 4–6 weeks despite continued dosing
  • CJC-1295 2mg weekly
  • GHRH analogue with albumin binding
  • 1.5–2× baseline (sustained)
  • 40–60% above baseline
  • Partially. Extends pulse duration
  • Once weekly subcutaneous
  • Moderate sustained response. Better than short-acting peptides but lower peak IGF-1 than MK-677, injection requirement limits compliance
  • Exogenous rhGH 4 IU daily
  • Direct GH replacement
  • 10–15× baseline
  • 80–150% above baseline
  • No. Suppresses endogenous production
  • Daily subcutaneous
  • Highest acute IGF-1 but suppresses natural GH axis within 2–4 weeks. Not viable for long-term research protocols requiring intact feedback loops
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