Ipamorelin
Ipamorelin
The most selective GH secretagogue
How it works
Ipamorelin selectively agonizes ghrelin receptors (GHS-R1a) on the pituitary to stimulate GH release without significantly affecting cortisol, prolactin, or ACTH. This high selectivity gives it a uniquely clean safety profile.
What the research explores
In published research, Ipamorelin has been studied in connection with the following. These describe findings reported in the literature — not approved uses, claims, or outcomes to expect.
- Stimulates selective, clean GH release
- Promotes fat loss without muscle catabolism
- Improves lean body composition
- Enhances sleep architecture and recovery
- Minimal effects on cortisol and prolactin
- Synergistic with GHRH analogs like CJC-1295
Compared to GHRP-2 and GHRP-6, Ipamorelin shows equivalent GH release with virtually no cortisol or prolactin elevation, making it the preferred research secretagogue.
Adverse events & gaps
Considered the most favorable safety profile among GHSs. Minimal reported side effects.
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