Ipamorelin

Research OnlyModerate Evidence
Written by dr-sarah-chen|Reviewed by Healthier Rx Editorial Board|Updated 2026-04-01|5 min read
Quick Facts
TypeGH Secretagogue
FDA StatusResearch Only
Evidence LevelModerate Evidence
Typical Dose100-300mcg
Frequency1-2x daily
Cycle Length8-12 weeks
Key GoalsMuscle Growth, Recovery, Anti-Aging

How It Works

Ipamorelin is a synthetic pentapeptide growth hormone secretagogue (GHS) that was first described in 1998 by Novo Nordisk. It consists of five amino acids (Aib-His-D-2-Nal-D-Phe-Lys-NH2) and acts as a selective agonist of the growth hormone secretagogue receptor (GHS-R1a), also known as the ghrelin receptor.

What sets Ipamorelin apart from other GH secretagogues like GHRP-6 and GHRP-2 is its remarkable selectivity. Studies have demonstrated that Ipamorelin stimulates GH release in a dose-dependent manner without significantly elevating ACTH, cortisol, prolactin, or aldosterone — even at doses far exceeding those needed for GH release. This selective profile makes it one of the best-tolerated GH peptides available.

Ipamorelin produces acute GH pulses that mimic natural pulsatile GH secretion. When combined with a GHRH analog such as CJC-1295 without DAC, the two peptides stimulate GH release through complementary pathways — GHRH receptor activation and ghrelin receptor activation — resulting in a synergistic and amplified GH pulse significantly greater than either peptide alone.

Benefits

  • Selective GH release — does not significantly elevate cortisol, prolactin, or appetite
  • Improved body composition — increased lean mass and reduced body fat
  • Enhanced recovery — faster tissue repair and reduced muscle soreness
  • Better sleep quality — deeper, more restorative sleep through GH optimization
  • Anti-aging effects — improved skin, energy, and overall vitality
  • Synergistic with GHRH peptides — particularly effective when stacked with CJC-1295

Side Effects

  • Very well-tolerated with the cleanest side-effect profile among GH secretagogues
  • Injection site reactions — redness, mild pain (common)
  • Headache — occasional, usually transient
  • Mild water retention — typically resolves after first 1-2 weeks
  • Tingling or numbness — mild paresthesia in some users
  • Light-headedness — occasionally reported immediately post-injection
  • No significant cortisol or prolactin elevation at standard doses

Dosing Protocol

ParameterDetails
Standard Dose100-300mcg per injection
Frequency1-2 times daily
AdministrationSubcutaneous injection
TimingBedtime (primary) and/or upon waking, on empty stomach
Cycle Length8-12 weeks on, 4 weeks off
Common StackCombined with CJC-1295 no DAC 100-200mcg at same times
FastingNo food 2+ hours before or 30 minutes after injection

What You Will Need

  • Ipamorelin lyophilized vial (typically 2mg or 5mg)
  • Bacteriostatic water (30mL)
  • Insulin syringes (1mL, 29-31ga)
  • Alcohol swabs
  • Sharps container

Frequently Asked Questions

References

  1. Ipamorelin, the first selective growth hormone secretagogueEuropean Journal of Endocrinology (1999). PMID: 10580762

    Characterization of Ipamorelin as the first GH secretagogue with selective GH release and no significant effect on ACTH, cortisol, or prolactin.

  2. Safety and pharmacokinetics of single and multiple ascending doses of the growth hormone secretagogue IpamorelinHormone Research in Paediatrics (2012). PMID: 22846232

    Phase 1 study demonstrating dose-dependent GH release with favorable safety and tolerability profile.

  3. Ipamorelin as a new growth hormone releasing peptide in the treatment of postoperative ileusEuropean Surgical Research (2008). PMID: 18765947

    Clinical evidence of Ipamorelin's GH-releasing effects and tolerability in a surgical patient population.

Protocols Featuring Ipamorelin

Medical Disclaimer

This content is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare provider before starting any new treatment or protocol. Read our full medical disclaimer.