Sermorelin

FDA-approved GHRH analog (first 29 amino acids of native GHRH) that stimulates physiological pulsatile growth hormone release while preserving natural feedback regulation.

Overview

Also Known As

Sermorelin Acetate, GRF 1-29 NH2, Geref, GHRH(1-29)NH2

Mechanism of Action

Binds GHRH receptor on anterior pituitary somatotrophs, stimulating pulsatile GH release. Preserves hypothalamic-pituitary feedback loop and somatostatin regulation. Produces physiological GH secretion patterns.

Product

Sermorelin Acetate, GRF 1-29 NH2, Geref, GHRH(1-29)NH2 vial
Dosing & Administration
Typical protocols and routes

Half-Life

10-20 minutes

Administration Routes

subcutaneousintravenous

Dosing Protocols

Reconstitute 10 mg vial with 2 mL bacteriostatic water, giving 20 equal doses. Draw 10 units on insulin syringe (marked 1-100) for a daily dose.
Research
Key findings and status

Key Research Findings

FDA-approved 1997 as Geref® for pediatric GHD. Walker (2006): 6-month adult therapy showed improved body composition, increased lean mass, decreased adiposity. Studies show enhancement of slow-wave sleep architecture.
Detailed Information

Sermorelin (sermorelin acetate) is a synthetic analog of the first 29 amino acids of naturally occurring growth hormone-releasing hormone (GHRH). It is the only GHRH analog that has received FDA approval, originally marketed as Geref® for diagnosing and treating growth hormone deficiency in children.

Mechanism of Action

Sermorelin binds to the GHRH receptor on somatotroph cells in the anterior pituitary gland, stimulating the synthesis and pulsatile release of endogenous growth hormone. Unlike exogenous GH administration, sermorelin preserves the hypothalamic-pituitary feedback loop, meaning GH release remains subject to somatostatin-mediated negative feedback. This results in a more physiological GH secretion pattern and reduced risk of supraphysiological GH levels.

Clinical Evidence

Sermorelin has a well-documented clinical history. It was FDA-approved in 1997 as Geref® for the treatment of idiopathic growth hormone deficiency in children with growth failure. Clinical trials demonstrated significant increases in growth velocity, IGF-1 levels, and lean body mass. In adult studies, sermorelin administration has been associated with improved sleep quality, increased lean body mass, decreased body fat, and improved skin elasticity.

Walker (2006) published data showing that 6 months of sermorelin therapy in adults resulted in significant improvements in body composition, including increased lean mass and decreased abdominal adiposity. The peptide has also been studied for its effects on sleep architecture, with research showing enhancement of slow-wave sleep.

Clinical Advantage

Sermorelin holds a unique position among GH-releasing peptides due to its history of FDA approval and extensive clinical safety data. Its mechanism preserves natural feedback regulation, making it a conservative first-line approach to GH optimization in research and clinical settings.

Safety & Legal

Side Effects & Warnings

Injection site reactions (pain, redness, swelling), facial flushing, headache, dizziness, nausea. Tachyphylaxis possible with prolonged use. Generally well-tolerated in clinical trials.

Legal Status

Previously FDA-approved as Geref. Available from compounding pharmacies and as research peptide.
Molecular Data
Chemical properties

Molecular Weight

3357.93 g/mol

Amino Acid Sequence

Tyr-Ala-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Met-Ser-Arg-NH2

Quick Facts

Class

GHRH

Research Status

Approved

Half-Life

10-20 minutes

Routes

subcutaneous
intravenous

Category

Growth Hormone Peptides