Peptide · Performance & growth
Ipamorelin is a selective growth hormone secretagogue. Prompts pulsatile GH release without the cortisol or appetite spikes seen with older GHRPs.
Ipamorelin is a selective growth hormone secretagogue. Prompts pulsatile GH release without the cortisol or appetite spikes seen with older GHRPs.
Ipamorelin is a synthetic pentapeptide and selective ghrelin receptor (GHSR-1a) agonist that stimulates pulsatile growth hormone (GH) release from the pituitary. Unlike older growth-hormone secretagogues (GHRP-2, GHRP-6), ipamorelin selectively binds the GH-release pathway without significantly affecting cortisol, prolactin, or appetite. This selectivity is the primary advantage.
Limited human trials; well-studied in animal models and small Phase II programs.
Compounded — not FDA-approved.
Common protocols:
Dosing in research and clinical-use contexts varies. Specific protocols should always be set by a prescribing clinician, not by patient-direct sources.
Generally well-tolerated. Reported side effects: injection-site irritation, transient water retention, mild fatigue in the first week, occasional headaches. Long-term safety of GH secretagogue use is not well-studied; theoretical concerns include effects on glucose metabolism and the same theoretical cancer-promotion concerns as exogenous HGH (though ipamorelin only stimulates physiologic GH release, not exogenous administration).
The standard stack is ipamorelin + CJC-1295 (with or without DAC) for additive GH release. Patients pursuing recovery often add BPC-157 + TB-500 for tissue-repair effects. Tesamorelin can substitute for CJC-1295 in patients prioritizing visceral fat reduction.
Most peptides discussed on this page are compounded products requiring a prescription from a licensed clinician. Reputable telehealth peptide programs include physician-led oversight, accredited compounding pharmacies, and clear regulatory framing. For weight-management GLP-1 programs, see our provider reviews.
Ipamorelin is a selective growth hormone secretagogue. Prompts pulsatile GH release without the cortisol or appetite spikes seen with older GHRPs.
Compounded — not FDA-approved.
Uses include: GH support, Recovery, Sleep quality (research). This is research and clinical-use context, not a recommendation. Always work with a licensed clinician.
Limited human trials; well-studied in animal models and small Phase II programs.
Reported dosing: 200–300 mcg subcutaneous before bed, often paired with CJC-1295. Actual dosing should always be determined by your prescribing clinician, not by online sources.
No. Ipamorelin stimulates your own pituitary to release endogenous GH in physiologic pulses. Exogenous HGH is administered as the hormone itself, producing sustained supraphysiologic levels. The risk profiles are different.
Modest effects on lean-mass retention and fat reduction are reported, but ipamorelin is not a 'bulking' compound. Effects are subtle and cumulative over months.
Sleep effects often within the first 1–2 weeks. Body composition and recovery effects build over 8–12 weeks.