Ipamorelin, the first selective growth hormone secretagogue.
European journal of endocrinology
Synthetic pentapeptide secretagogue
Also indexed as: NNC-26-0161
The foundational linked study is preclinical. A separate human postoperative-ileus trial does not establish anti-aging or recovery benefit.
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12 glossary terms used in this profile
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Definitions explain the words—not whether a molecule works or is safe. Research education only, not medical advice.
Ipamorelin is a synthetic pentapeptide developed as a growth hormone secretagogue. Its research history includes preclinical endocrine work and a separate clinical gastrointestinal-motility study.
Ghrelin / GH–IGF-1
Stimulates GH release through ghrelin-receptor/secretagogue signaling, rather than the GHRH receptor. Selectivity reported in preclinical models does not guarantee absence of adverse effects in people.
A biological pathway describes a proposed or observed interaction—not necessarily a demonstrated health outcome.
Decode the terminology in our glossaryHuman evidence is still developing
Studies in people exist, but the findings may be small, narrow, mixed or still need confirmation. A hormone or cell marker is not necessarily a health benefit.
For this research: The foundational linked study is preclinical. A separate human postoperative-ileus trial does not establish anti-aging or recovery benefit.
An editorial guide—not a validated score, a percentage, a safety rating or an approval badge. Regulatory status is separate. More research does not mean fewer risks.
Mechanistic laboratory evidence is not separately assessed in this selected-source summary; see references and their study types.
The foundational paper uses rat pituitary cells, rats and swine to investigate GH release.
Associations, biomarker studies and anecdotes cannot establish treatment causality; no observational result is used here to infer clinical effectiveness.
A randomized postoperative-ileus trial exists (PubMed 25331030); it does not validate performance or anti-aging uses.
No FDA-approved finished drug for this molecule is identified in this edition. Investigational use, published research or compounding does not establish FDA approval.
GH signaling and gastrointestinal motility research.
These describe scientific questions, not prescribing recommendations. A research grouping does not establish combination safety or clinical effectiveness.
Explore research by health goalFDA notes serious adverse events including deaths in an intravenous motility study and insufficient safety information for other injectable routes; this does not by itself establish causality.
This is not an exhaustive safety or contraindication list. An absence of reported harm is not proof of safety. Pregnancy, breastfeeding, cancer history, endocrine disease and concurrent medicines can materially change risk. Unregulated preparations add identity, contamination and sterility risks.
Read FDA’s compounding safety informationNot FDA-approved
No FDA-approved finished drug for this molecule is identified in this edition. Investigational use, published research or compounding does not establish FDA approval.
Regulatory status and evidence strength are different. A nomination for compounding, a clinical-trial registration or a “research use only” label is not approval. International rules vary; consult the current regulator and product label.
Ipamorelin, the first selective growth hormone secretagogue.
European journal of endocrinology
Randomized postoperative-ileus study of ipamorelin
International Journal of Colorectal Disease
Disease-specific study cited by FDA; not a performance or anti-aging trial.
Matched bibliographic records confirm a publication’s identity, not the validity of every claim. Selected sources are not a systematic literature review.
These open search results, not additional verified citations. Trial registration is not evidence that a treatment works.
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Education, not a prescription. Research summaries are not medical advice, dosing instructions, or an offer to sell. Mechanistic findings do not establish clinical effectiveness. US regulatory status is product- and indication-specific and may change. Discuss health decisions with a licensed clinician.