Ipamorelin
A selective ghrelin-receptor agonist studied for stimulating GH release with less prolactin/cortisol impact than older GHRPs. Originally placed on FDA Category 2 list (September 2023), then removed September 27, 2024 when the nominator withdrew. FDA still lists it under 'Other bulk drug substances that may present significant safety risks.' Regulatory status remains uncertain.
Written by WhatPeptide Editorial Team · Last updated 2026-03-17
Half-life
Approximately 2 hours
Dosage range
100-300 mcg once to three times daily (published research context)
Administration
Subcutaneous injection
Research level
Moderate
How Ipamorelin works
Ipamorelin binds the growth hormone secretagogue receptor (GHSR-1a) to stimulate pituitary GH release in a pulsatile pattern. Compared with earlier GHRPs, it appears more selective with less ACTH/prolactin spillover in small studies. Real-world body-composition data remains limited.
Also known as: NNC 26-0161, Selective ghrelin mimetic
Research relevance
Side effects & safety
Contraindications
Consult a healthcare provider before use if any of these apply to you.
Key studies
-
Gobburu JV et al. — PK/PD modeling of ipamorelin in human volunteers
Terminal half-life 2 hours (IV); single GH pulse peak at 0.67 hours; dose-proportional PK
PubMed 1999 -
Raun K et al. — Ipamorelin, the first selective growth hormone secretagogue
GHSR-1a agonism; no ACTH/cortisol elevation even at 200× GH-releasing ED50
PubMed 1998
FAQ
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