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Sermorelin

GHRH(1-29) peptide analogue

Growth-hormone diagnost…deficiency research
Generic peptide vial illustrationSermorelin
Entity typePeptide analogue / modified peptide
Evidence reviewed2026-09-18
Canonical recordSERMORELIN
Page updated2026-09-20
Evidence profileEstablished human endocrine pharmacology; historical clinical use; lifestyle benefits unproven
Human evidenceSee evidence
Regulatory statusHistorical approval only
Choose your depthStart simple, then open the evidence or technical detail only if you need it.
Quick answerPlain languageEvidenceOutcomes and studiesStudiesPrimary recordsTechnicalMechanism, route and identifiers

In plain English

30-second evidence answer

What does the evidence mean in simple terms?

Sermorelin has human evidence showing that it can stimulate the growth-hormone pathway in defined clinical settings. That does not establish general anti-ageing, fat-loss, muscle-building or longevity benefits in healthy adults.

Still uncertain: General anti-ageing, body-composition, performance or longevity benefits in otherwise healthy adults.

New to terms such as “preclinical”, “randomized” or “investigational”? Use the plain-English glossary →

What does the evidence mean in simple terms? table
What is it?GHRH(1-29) peptide analogue
Entity typePeptide analogue / modified peptide
Research focusGrowth-hormone diagnostic/deficiency research
Human evidenceNative GHRH(1-29)/sermorelin has genuine human endocrine and diagnostic evidence. In a tiny 6-week study of older men, nightly GHRH increased nocturnal GH but did not significantly improve IGF-I or DEXA body composition.
Regulatory statusHistorical FDA marketing approval existed for Geref (sermorelin acetate); this does not confer approval on generic research-market sermorelin.
Main limitationsGeneral anti-ageing, fat-loss, muscle-building or longevity efficacy in otherwise healthy adults.
SafetyGH-axis adverse effects and contraindications are context-specific; unregulated products add purity/identity uncertainty.
Evidence reviewed2026-09-18
i
Native GHRH(1-29)/sermorelin has genuine human endocrine and diagnostic evidence. In a tiny 6-week study of older men, nightly GHRH increased nocturnal GH but did not significantly improve IGF-I or DEXA body composition.
Outcome-level evidence

Evidence is not one score.

Each record below answers a narrower question about an outcome, population or context. Evidence status and the study finding are shown separately so strong evidence is not mistaken for a positive effect.

How to read this →

Growth-hormone stimulation / diagnostic reserve

Human evidence
Established human endocrine pharmacology

Context: Children, adolescents and adults in endocrine testing

Finding: Human target engagement is well established for native GHRH(1-29).

Uncertainty / evidence gap: Target engagement does not establish lifestyle benefits.

Body composition / anti-ageing claims

Human evidence
Very small human study with null body-composition findings

Context: Healthy older men

Finding: GH secretion can increase without producing broad anti-ageing/body-composition effects over short trials.

Uncertainty / evidence gap: No DEXA body-composition improvement in this small study.

Verified 2026-09-18Primary source ↗
Evidence rule: an outcome-specific evidence label is not a recommendation, a safety rating or an overall score for the compound.

Evidence synthesis

  • ✓Human target engagement is well established for native GHRH(1-29).
  • ✓GH secretion can increase without producing broad anti-ageing/body-composition effects over short trials.

Important limitations

  • !Historical diagnostic/deficiency context differs from modern anti-ageing marketing.
  • !N=11, short duration.

Selected study & evidence records

Comparison of GHRH(1-40) and GHRH(1-29)NH2 in young adults and children

1986 · Human diagnostic/physiology study · n=142

GHRH(1-29)NH2 produced GH responses useful for testing pituitary GH reserve; responses varied by underlying diagnosis.

Study detail → Primary source ↗

Nightly GHRH(1-29) in healthy older men

1997 · Randomized placebo-controlled clinical physiology study · n=11

Nocturnal GH increased, but IGF-I did not significantly increase; 2 of 6 strength/performance measures improved while DEXA body composition did not change.

Study detail → Primary source ↗

Safety and unknowns

GH-axis adverse effects and contraindications are context-specific; unregulated products add purity/identity uncertainty.

Historical clinical use provides more human exposure than most research peptides, but modern anti-ageing/body-composition use is not the same indication.

Technical details

Mechanism / biologyStimulates pituitary GHRH receptors to release endogenous GH.
Route / formulation boundaryCurrent authorization and product quality must be checked by jurisdiction/product.
Identity / data-quality noteUse the canonical compound identity and studied formulation when interpreting evidence.
Study / label regimen evidenceHuman pharmacology dosing verified. A small endocrine study tested IV GHRH(1-29)-NH2/sermorelin at 0.1 and 1.0 micrograms/kg as pulsed challenge doses. This is pharmacology evidence, not a routine self-use regimen.
Identifiers & alternate namesSermorelin Acetate · GHRH(1-29)-NH2

Source depth & provenance

WhichPeps does not rely on a single headline study when the evidence base is broader. Primary research, registries, regulators and supporting records are kept distinct.

2structured study records
2outcome records
8linked source records

How to read these counts: they show evidence coverage, not evidence strength. One large, well-designed study can be more informative than several weak or indirect records.

Show supporting and discovery sources

Study pages above contain the records used for public evidence summaries. The links below include supporting, regulatory and literature-discovery sources; a registry or search result is not treated as proof of benefit.

Evidence rule: WhichPeps keeps human, animal, laboratory, regulatory and product/formulation evidence distinct. Common names help people find the page; they do not change the underlying scientific identity.