Ipamorelin
Highly selective GH secretagogue and GHRP. Studied for its selective stimulation of GH without significant cortisol or prolactin elevation — considered the "cleanest" GHRP in research.
Ipamorelin is a synthetic pentapeptide and a selective growth hormone secretagogue. It activates the ghrelin receptor to stimulate GH release but is notable for its selectivity — it produces GH pulses without significantly raising cortisol, prolactin, or ACTH at research doses. This selectivity distinguishes it from GHRP-2 and GHRP-6 and has made it a preferred GHRP in research contexts.
- Selective GH stimulation without significant cortisol, prolactin, or ACTH elevation at research doses.
- Phase 1 and 2 human trials confirmed its selectivity and tolerability.
- Development was discontinued for postoperative ileus indication but the compound is widely used in research.
- No large body composition trials have been published with ipamorelin specifically.
Ipamorelin's pharmaceutical development program was discontinued — it did not advance to approval for any indication. The body composition and anti-aging applications that generate research interest have not been studied in large, controlled human trials. Its selectivity advantage over other GHRPs is meaningful, but the long-term effects of sustained GH stimulation through ipamorelin use are not established.
Ipamorelin binds to the ghrelin receptor in the pituitary gland, which signals the pituitary to release a pulse of GH. Unlike GHRP-2 and GHRP-6, which also activate this receptor but simultaneously trigger cortisol and prolactin release, ipamorelin appears to achieve GH release with much less activation of those other pathways. Think of it as a more precise key that opens the GH release door without accidentally opening the cortisol and prolactin doors at the same time. This selectivity is considered an advantage in research settings because it allows researchers to study GH effects more cleanly without the confounding effects of elevated cortisol.
Ipamorelin was studied in human trials without significant safety concerns identified. It is not FDA-approved. The selectivity profile — minimal cortisol and prolactin stimulation — is considered favorable compared to other GHRPs. Standard considerations about elevated GH and IGF-1 apply with repeated use. Research-grade purity should be confirmed. It is not approved for any medical use.
This compound has been studied in Phase 1 or Phase 2 human trials. Evidence is encouraging but more large-scale trials are needed.
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