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Sermorelin

GHRH (1-29), GRF 1-29 NH2, Sermorelin acetate

Quick Stats
Studies 223
Trials 41
Score 2
1996 pubmed

Once daily subcutaneous growth hormone-releasing hormone therapy accelerates growth in growth hormone-deficient children during the first year of therapy. Geref International Study Group.

Thorner. M M; Rochiccioli. P P; Colle. M M; Lanes. R R; Grunt. J J; Galazka. A A; Landy. H H; Eengrand. P P; Shah. S S

Key Findings

  • Daily subcutaneous sermorelin (30 µg/kg) increased height velocity from ~4 cm/yr to ~8 cm/yr after 6 months.
  • Growth response was sustained at 12 months (≈7.2 cm/yr) and 74% of children were classified as good responders at 6 months.
  • No significant safety concerns: unchanged fasting glucose, IGF‑1, and normal clinical chemistry throughout the year.

Practical Outcomes

  • For biohackers, this study shows that sermorelin can effectively boost growth hormone activity in people who are truly GH‑deficient, with a good safety record at the tested dose. However, the results come from pre‑pubertal children, so they don’t directly translate to healthy adults seeking anti‑aging or performance benefits. Use the 30 µg/kg daily dose as a reference point only if you have a confirmed GH deficiency and medical supervision.

Summary

A year‑long study gave kids who lack growth hormone a daily shot of sermorelin (30 µg per kg). Their growth speed roughly doubled in the first six months and stayed high after a year, with no major side effects or changes in blood sugar or IGF‑1 levels.

Abstract

The efficacy and safety of 1 yr of GH-releasing hormone [GHRH-(1-29)] therapy in GH-deficient children were determined. One hundred and ten previously untreated prepubertal GH-deficient children were treated for up to 1 yr in a multicenter, open label study with 30 micrograms/kg GHRH-(1-29)/day, sc, given at bedtime. Eighty-six of the 110 patients were eligible for efficacy analysis. The main outcome measures, monitored every 3-6 months, were linear growth enhancement (height velocity), bone age progression, and safety measures including clinical chemistry. The mean height velocity for the group increased from 4.1 +/- 0.9 cm/yr at baseline to 8.0 +/- 1.5 and 7.2 +/- 1.3 cm/yr after 6 and 12 months of therapy, respectively. At 6 months, 74% of the children were considered to have a good response to GHRH. The ratio of the change in bone age to height age was not significantly different from unity at 12 months (1.04 +/- 0.58; P = 0.63). No adverse changes in general biochemical or hormonal analyses were noted. No change in fasting glucose concentration or excessive generation of insulin-like growth factor I occurred, and overall GHRH was well tolerated. We conclude that GHRH administered as a once daily dose of 30 micrograms/kg GHRH.(1-29), s.c., was effective in increasing height velocity in GH-deficient children.

Study Information

Provider

pubmed

Year

1996

DOI

10.1210/jcem.81.3.8772599