Peptides
Evidence: moderate_human
Ipamorelin is a pentapeptide (Aib-His-D-2-Nal-D-Phe-Lys-NH2) that acts as the first selective growth hormone secretagogue receptor (GHS-R1a/ghrelin receptor) agonist. Unlike other GHRPs, it selectively stimulates GH release without significantly affecting ACTH, cortisol, prolactin, or aldosterone — even at doses 200-fold above the ED50 for GH release. This selectivity profile is comparable to GHRH itself but operates through the distinct ghrelin receptor on pituitary somatotrophs.
Standard: Research indicates 200-300 mcg administered 1-3 times daily via subcutaneous injection.
Maintenance: Research indicates 100-200 mcg at bedtime for maintenance.
Administration: subcutaneous
Timing: Best administered at bedtime for synergy with natural GH peak. Also effective upon waking and post-workout. Always on empty stomach.
Duration: 12-24 week cycles with 4-8 week breaks.
Ipamorelin is widely considered the cleanest GH secretagogue due to its unique selectivity — no cortisol spike, no prolactin increase, minimal hunger stimulation. The CJC-1295 no-DAC + Ipamorelin combination exploits synergy between GHRH (hypothalamic) and GHRP (pituitary) pathways for amplified GH release. Saturation dose is approximately 1 mcg/kg. Commonly prescribed by anti-aging and optimization clinics as a first-line GH optimization peptide.
Compounding pharmacy (503A/503B) or research-grade supplier. One of the most commonly compounded peptides.
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