Scientific context only. Not medical advice, not a recommendation to use.
At a glance
Synthetic analogue of the first 29 amino acids of human GHRH. Stimulates pulsatile growth-hormone secretion from the pituitary. Formerly FDA-approved as Geref Diagnostic, now withdrawn in many markets — compounding and research use dominate.
Researched for
GH stimulationDiagnosis of GH deficiencyAnti-aging (anecdotal)Sleep quality (anecdotal)
Official status
US: Research only
Originally FDA-approved as Geref Diagnostic; after market withdrawal only available via compounding or as research substance.
Reading note. The distribution shows on which evidence tier each observation sits. Strong colours mark stronger evidence — weaker tiers are deliberately visible, not hidden.
3 observations · 3 tiers
Human RCT
1
Human trial
1
Anecdotal
1
03
What the studies show
Human RCT
Mensch, klinische Studien
Thorner MO et al. 1997
Stimulation of growth-hormone release
What does NOT follow: Pharmacological action on the GHRH receptor well established; clinical endpoints depend on indication.
Human trial
Mensch, klinischer Einsatz
Thorner MO et al. 1997
Use as a diagnostic provocation test for GH deficiency
What does NOT follow: Diagnostic use historically established; therapeutic indication withdrawn in many markets.
Anecdotal
—
Claimed anti-aging and body-composition effects
What does NOT follow: Outside the diagnostic indication, no controlled human studies on anti-aging endpoints.
04
Where studies disagree
Open question
Is sermorelin a meaningful intervention for healthy aging or anti-aging?
POSITION A
GHRH activity at the receptor and physiological GH stimulation are established — theoretically appealing.
POSITION B
Clinical anti-aging outcome trials (morbidity, mortality, function) are missing. Existing knowledge on elevated IGF-1 activity warrants caution.
CURRENT STATE · Anti-aging indication is not established. Diagnostic use is historically documented.
05
Pharmacokinetics
Theoretical concentration curve at a half-life of 0.2 h. Pure pharmacokinetic model — not a dosing recommendation.
Which routes of administration the available studies describe — neutral reporting, not a usage guide.
Subcutaneous
Standard route in clinical use and provocation tests.
Intravenous
Historically used in provocation tests.
07
Known adverse events from studies
Factual reporting of what studies observed. Not a safety statement for individual use.
Human RCT
Flushing
Classically described in provocation-test data; mostly transient.
häufig / common
Human trial
Headache
Reported in clinical use.
gelegentlich / occasional
Human trial
Injection-site reactions
Local reactions as with many peptide injections.
vereinzelt / sporadic
07b
Interactions & combinations
Documented interactions and contraindications from studies, prescribing information and guidelines. Where no data exists, this is stated.
Reporting of risks, NOT a combination guide. The absence of an entry does not mean „safe to combine“ but „not sufficiently studied“.
No documented interactions recorded
We have not yet found robustly documented interactions for this peptide. This does NOT mean none exist — the data is limited.
08
Risks & hygiene aspects in the literature
What regulatory and scientific literature reports on risks, sterility and identity in non-pharmaceutical sources — descriptive, not a hygiene guide.
Status after FDA market withdrawal
Regulatory documents show the market withdrawal was not safety-related. Today's sources are mainly compounding pharmacies or the grey market — neither with the pharmaceutical quality control of the approved formulation.
10
Anecdotal observations
Weakest evidence tier — not supported by studies
Reading note. This section gathers popular claims from communities and forums. They are explicitly marked as weakest-tier evidence. Unblinded self-reports are particularly prone to placebo, recall and confirmation biases.
Why no amounts or protocols are listed here. We deliberately show only WHAT communities report — not in what amount or how it is used. Anecdotal "doses" or "biohacker protocols" are neither verified nor standardised nor safe; publishing them would be a usage guide, which we do not provide on principle. Specific amounts belong in a conversation with a doctor, not in a forum.
Improved sleep and well-being under "anti-aging" use
Common claim in associated communities and private-practice offerings
Not supported by studies: Anti-aging indication is not established by RCTs; endpoints are subjective and prone to expectation effects.
11
Legal status by country
Country
Status
Note
Checked
United States
Research only
Originally FDA-approved as Geref Diagnostic; after market withdrawal only available via compounding or as research substance.
2026-05
Germany
Unapproved
Currently no medicinal-product authorisation in Germany.
2026-05
12
Reconstitution calculator
Pure mg/mL maths — works like a calculator. Not a usage recommendation.
Peptides ship as a dry powder. Once dissolved in a liquid (reconstitution), this calculator answers a single question: how much substance is in one millilitre of solution afterwards?
1Enter the vial's substance amount (printed on the label).
2Enter how much solvent you add.
3Result = concentration in mg per mL.
Printed on the label
/
Liquid you add
=
2.50
mg / mL
5 mg in 2 mL gives 2.50 mg/mL — each millilitre contains 2.50 mg of substance.