ID: sermorelin
Aliases: SERMORELIN, SERMORELIN ACETATE, Geref, GHRH(1-29) amide
Type: compound
Route/form: subcutaneous injection in historical/compounded contexts
Status: withdrawn_legacy_or_compounded
Evidence level: early human
Best data tier: early human
Support scope: review/regulatory
Source types: regulatory_review, review
Linked sources: 2
Broad outcomes: Hormones / fertility / sexual health, Longevity / mitochondrial / redox, Muscle growth / performance / recovery, PEDs / AAS / thermogenics
Reading note: These are curation notes anchored to linked sources, not a clinical recommendation or protocol.
Targets / mechanism
- GHRH receptor agonism
- pulsatile growth hormone release
- GH deficiency diagnostic/therapy context
Optimization domains
- growth hormone
- endocrine
- pediatrics
- anti aging
Research basis
- Sermorelin has clinical literature and regulatory history in pediatric GH-deficiency diagnosis/treatment contexts.
- Mechanistically it is upstream GHRH stimulation, so the most defensible claim is pituitary GH release when reserve is present.
- It is a useful comparator to somatropin because it depends on endogenous axis capacity rather than replacing GH directly.
Limits, risks, and missing evidence
- Adult wellness, anti-aging, recovery, or body-composition claims are much weaker than the pediatric GH-deficiency context.
- Response depends on pituitary reserve and baseline GH/IGF physiology.
- GH-axis adverse effects and monitoring remain relevant.
Risk flags
- endocrine axis
- gh igf1 axis
- pediatric context
- outcome extrapolation
Linked papers, labels, and reviews
- FDA Federal Register: sermorelin acetate was not withdrawn from sale for reasons of safety or effectiveness
regulatory_review / govinfo_sermorelin_not_withdrawn_2013
Regulatory history for sermorelin/Geref. - Sermorelin: a review of its use in the diagnosis and treatment of children with idiopathic growth hormone deficiency
review / pubmed_sermorelin_gh_deficiency_review_1999
Clinical review in pediatric GH deficiency; not adult wellness evidence.