Skip to content
Recovery & Performance PeptidesRecovery research and practical context
Source comparison

CJC-1295 Ipamorelin Protocol Fat Loss: Comparison

Ipamorelin Solo Ghrelin receptor agonist. Triggers GH pulse (20–30 min duration) 1–2×/day 0.5–1.2kg visceral fat High Minimal Short GH pulse limits lipolytic window. Works but requires perfect timing CJC-1295 Solo (no DAC) GHRH analogue. Extends endogenous GH

This comparison does not assign a generated winner or score.

  • Ipamorelin Solo
  • Ghrelin receptor agonist. Triggers GH pulse (20–30 min duration)
  • 1–2×/day
  • 0.5–1.2kg visceral fat
  • High
  • Minimal
  • Short GH pulse limits lipolytic window. Works but requires perfect timing
  • CJC-1295 Solo (no DAC)
  • GHRH analogue. Extends endogenous GH pulse duration
  • 0.3–0.8kg visceral fat
  • Extends pulse but lacks amplitude. Insufficient for meaningful fat oxidation
  • CJC-1295 + Ipamorelin
  • Synergistic: ipamorelin initiates pulse, CJC-1295 extends it (2–4 hr window)
  • 1.5–2.2kg visceral fat
  • Gold standard. Sustained GH elevation produces measurable fat loss without muscle catabolism
  • CJC-1295 with DAC + Ipamorelin
  • DAC version has 6–8 day half-life. Creates steady-state GH, not pulsatile
  • Once weekly CJC + daily ipamorelin
  • 0.8–1.4kg visceral fat
  • Moderate
  • Moderate (prolonged GH suppresses natural pulse)
  • Incompatible pharmacokinetics. DAC negates the pulsatile benefit of ipamorelin
  • GHRP-6 + CJC-1295
  • Older ghrelin agonist. Triggers GH but also cortisol and appetite increase
  • 1.2–1.8kg visceral fat
  • High (cortisol spikes, prolactin elevation)
  • Effective for GH release but appetite rebound and cortisol make adherence difficult
More references

Related material