FDA Drug Label
GEREF (sermorelin acetate) for injection - Prescribing Information
Serono, 1997
GHRH 1-29
Sermorelin acetate (GHRH 1-29) is a synthetic analog of the first 29 amino acids of endogenous growth hormone-releasing hormone. FDA-approved for diagnosing and treating GH deficiency, it stimulates the pituitary gland to produce and secrete growth hormone naturally — a preferred alternative to exogenous HGH therapy for physiological GH optimization. Available by prescription through compounding pharmacies and telehealth providers.
Trend index
Overview
Sermorelin acetate (GHRH 1-29) is a synthetic analog of the first 29 amino acids of endogenous growth hormone-releasing hormone. FDA-approved for diagnosing and treating GH deficiency, it stimulates the pituitary gland to produce and secrete growth hormone naturally — a preferred alternative to exogenous HGH therapy for physiological GH optimization. Available by prescription through compounding pharmacies and telehealth providers.
Community
Positive 90% · Neutral 10% · Negative 0%
Median: 200–400 mcg · Most common: 200–400 mcg
Among repeat reporters, 81% said they felt similar to their last entry, 8% more positive, and 12% more negative.
Overall, repeat reporters leaned more negative than their previous entry.
Median gap between entries: 105 days · Based on 26 repeat reporters
Research
FDA Drug Label
Serono, 1997
PubMed
Ghigo et al., 2008
Help
This page summarizes 36 anonymized self-reports from PeptIQ users who track Sermorelin, including commonly reported effects and co-tracked peptides. These are observational patterns, not clinical outcomes.
2 sources are linked on this page, including PubMed articles, clinical trial registries, and FDA labels where applicable. Citations describe published research — not recommendations.
This wiki does not assess safety or recommend use. Sermorelin is listed as FDA Approved. Consult a licensed clinician for personal medical decisions.
Research, primarily in animal models, suggests Sermorelin may have a wide range of therapeutic potentials due to its ability to promote angiogenesis (formation of new blood vessels), stimulate collagen synthesis, and modulate inflammatory responses.
SourceSermorelin is not approved by the FDA for any human use. There is no legal basis for selling it as a drug, food, or dietary supplement in the United States. The FDA has classified Sermorelin as a Category 2 bulk drug substance, which explicitly prohibits licensed compounding pharmacies from using it in compounded medications.
SourceThe safety and effectiveness of Sermorelin have not been thoroughly evaluated in humans through rigorous clinical trials. This lack of human data means that safe dosages, short-term side effects, and long-term health consequences are largely unknown.
SourceWhile there are over 200 published studies on Sermorelin, the vast majority are animal or in vitro (cell) studies. These preclinical studies consistently show positive results across various tissue types. However, there is a significant lack of comprehensive human clinical trial data.
Source