Growth Hormone Release. Ipamorelin is a selective growth hormone secretagogue that stimulates GH release through the ghrelin/GHS receptor. It is...
Ipamorelin is a selective growth hormone secretagogue that stimulates GH release through the ghrelin/GHS receptor. It is considered one of the most selective GH-releasing peptides — primarily stimulating GH without significantly affecting cortisol, prolactin, or aldosterone, a notable advantage over GHRP-6 and GHRP-2.
Ipamorelin acts as a ghrelin mimetic, binding to GHS-R in the pituitary gland and triggering calcium-dependent GH release. Unlike GHRP-6, it does not significantly stimulate appetite, and unlike GHRP-2, it has minimal effects on cortisol and prolactin. It is frequently combined with CJC-1295 (no DAC) for synergistic GH pulsing.
Important: The evidence base for Ipamorelin varies by application. Many findings are from preclinical (animal or in vitro) studies. Large-scale human clinical trials may not be completed. Always evaluate the quality of evidence before drawing conclusions.
Generally well-tolerated. Reported effects include transient headache, flushing, dizziness, and injection site reactions. Water retention and joint stiffness may occur with sustained use.
Ipamorelin remains on the FDA's Category 2 (restricted) list after the 2026 reclassification. Subject to ongoing litigation and further PCAC review. Available as a research chemical but cannot be legally compounded by 503A pharmacies.
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