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Human Growth Hormone (Somatropin)
Recombinant human growth hormone is one of the best-evidenced hormone therapies that exists — decades of trials across multiple real indications, since 1985. But almost none of that evidence applies to the reason most people buying it from grey-market sources want it: to build muscle or reverse aging as a healthy adult. For that use, there's no comparable trial base, and it's a prohibited substance in every major sport.
On this page
In brief
Should you care? Yes — this is the actual hormone every GH-secretagogue page on this site (sermorelin, CJC-1295, ipamorelin, hexarelin, GHRP-2/6, tesamorelin) exists to substitute for or provoke the release of.The short version
- Genuinely approved for pediatric and adult GH deficiency and several other named conditions since 1985.
- A real historical safety chapter: cadaver-derived GH caused a documented Creutzfeldt-Jakob disease outbreak before recombinant product replaced it.
- Prohibited in all sport, at all times — no trial evidence supports the muscle-building/anti-aging use it's sold for off-label.
What it's actually approved for
Recombinant hGH was first approved in 1985 as Protropin (somatrem, Genentech) — the first recombinant pharmaceutical product sold by a biotech company — for severe pediatric growth hormone deficiency, replacing the cadaver-pituitary-derived hormone used before it. Humatrope (somatropin, Eli Lilly) followed in 1987. Today's approved indications across various somatropin brands include pediatric GH deficiency, Turner syndrome, Prader-Willi syndrome, Noonan syndrome, SHOX deficiency, small-for-gestational-age growth failure, chronic renal insufficiency, adult GH deficiency, and (as Serostim) HIV-associated wasting.
A real, ugly safety chapter worth knowing
Before recombinant hGH, growth hormone was extracted from human cadaver pituitary glands, used to treat roughly 7,700 US patients from the 1960s through the 1980s via the National Hormone and Pituitary Program. That practice caused a real, documented outbreak of iatrogenic Creutzfeldt-Jakob disease: at least 226 cases worldwide, 29 of them in the US, with reported incubation periods of 5 to 42 years (mean 17 years) — and one case reported with a 48.3-year incubation period. US cases were found only in patients treated before 1977, when a new purification procedure using column chromatography was introduced. This is why recombinant hGH replaced cadaver-derived hormone entirely, and it's relevant context, not a knock against today's recombinant product.
Prader-Willi: a real warning worth knowing
Current somatropin labels carry reports of sudden death in Prader-Willi syndrome patients who were severely obese, had upper-airway obstruction, sleep apnea, or an unidentified respiratory infection at treatment initiation — this is FDA-mandated label language, not an outside critique, and a genuine warning worth knowing rather than marketing caution.
The anti-aging/bodybuilding use
hGH is prohibited at all times under WADA's S2 category (peptide hormones, growth factors and related substances), detectable via an isoform test that distinguishes exogenous 22kDa GH from the body's natural mix of isoforms. We did not find controlled trial evidence supporting muscle-building or anti-aging claims in GH-sufficient healthy adults comparable to the trial base behind its approved indications — that gap, between "real approved hormone" and "what it's sold for online," is the story here.
A real hormone doesn't mean a tested use
Decades of trial evidence exist for hGH in deficiency states. None of that evidence transfers automatically to a GH-sufficient adult using it for muscle or anti-aging purposes — a different population, and a different, largely untested, question.
References
- Genentech/FDA approval history: Protropin (somatrem), 18 October 1985; Humatrope (somatropin), 1987.
- CDC, "Cadaveric Human Growth Hormone–Associated Creutzfeldt-Jakob Disease with Long Latency Period, United States," Emerg Infect Dis 2025 (PMID 40439459); background case counts (≈226 worldwide/29 US, National Hormone and Pituitary Program) per CDC/PMC iCJD literature (PMID 23750511).
- Current somatropin FDA labeling (e.g. Genotropin, Norditropin) — Prader-Willi syndrome sudden-death warnings and contraindications.
- WADA Prohibited List, S2 category (peptide hormones, growth factors and related substances, 2026 edition) — GH prohibited at all times; isoform-based detection method.