Sermorelin vs Tesamorelin: Differences, Evidence and Status

By Editorial team. Updated Oct 15, 2026. Awaiting expert review

Sermorelin vs Tesamorelin at a glance

FactSermorelinTesamorelin
Also known asGRF (1-29), Geref, Sermorelin acetateEgrifta, Tesamorelin acetate
What it isSynthetic GHRH(1-29) analogue (formerly approved in the US)Synthetic GHRH analogue (approved medicine in the US)
Evidence levelFormerly approved drug (approvals withdrawn)Approved drug (in at least one market)
Approved productsGeref (discontinued) (US, 1990); Geref (discontinued) (US, 1997)Egrifta (US, 2010)
United StatesApproved by the FDA as Geref in 1990 and 1997; both products were discontinued in 2008, and FDA withdrew both approvals effective June 18, 2009 [14][15][2].Prescription medicine approved as Egrifta in November 2010 [5].
United KingdomNo UK-licensed medicine containing sermorelin appears in the MHRA products database [16].No UK-licensed medicine containing tesamorelin appears in the MHRA products database [22].
European UnionNo medicine containing sermorelin is authorized in the EU, according to EMA's central and Article 57 product data [17][18].An EU marketing application for Egrifta was withdrawn in 2012; no tesamorelin medicine is authorized [23][18].
CanadaNo product containing sermorelin appears in Health Canada's Drug Product Database [19].Egrifta was marketed in Canada but its listing is cancelled [24].
AustraliaSchedule 4 (prescription-only) in Australia's Poisons Standard, which also lists growth hormone releasing hormones (GHRHs), including those named separately in Schedule 4, among poisons that must not be possessed without authority (Appendix D) [20].Tesamorelin is not named, but Australia's Poisons Standard lists growth hormone releasing hormones (GHRHs) in Schedule 4 with Appendix D possession controls [20].
Sport (WADA)Named as a prohibited growth hormone-releasing hormone analogue under S2 [11].Named as a prohibited growth hormone-releasing hormone analogue under S2 [11].
Vendors we track62 vendors78 vendors
Our lab testsNone yetNone yet
Regulatory rows summarize official sources, checked Oct 15, 2026; rules change, so follow the numbered sources. Not legal or medical advice, and we don't publish dosing or usage instructions.

Sermorelin and tesamorelin are both copies of growth hormone-releasing hormone (GHRH), and both prompt the pituitary gland to release the body’s own growth hormone [1, 7]. Sermorelin is a shortened, 29-amino-acid version; tesamorelin is the full 44-amino-acid hormone with a small chemical group added that slows its breakdown [1, 3, 4]. The bigger difference is regulatory. Tesamorelin is a current US prescription medicine, Egrifta, for one condition: excess abdominal fat in people with HIV [5, 7]. Sermorelin was approved in the US as Geref, but the products were discontinued in 2008 [2].

What each one is

Sermorelin is a 29-amino-acid analogue of human GHRH and the shortest synthetic peptide with the hormone’s full biological activity [1]. A 2026 review describes it as GHRH(1–29) and as short-acting, with a disappearance half-time of about four minutes [13]. FDA approved it as Geref: in 1990 as a test of the pituitary’s ability to release growth hormone, and in 1997 to treat idiopathic growth hormone deficiency in children with growth failure [2]. EMD Serono, which held both applications, discontinued the products in 2008, and in 2013 FDA determined that they had not been withdrawn for reasons of safety or effectiveness [2].

Tesamorelin, developed under the code TH9507, is GHRH(1–44), the full-length hormone [4]. Its one change is a trans-3-hexenoyl group attached to the first amino acid [3, 13]. In laboratory and animal tests, this made it resistant to DPP-4, an enzyme that inactivates natural GHRH, and slowed its breakdown in plasma [3].

How the evidence compares

Tesamorelin has the stronger human evidence, for a narrow use. In a 26-week trial of 412 people with HIV and excess abdominal fat, visceral (deep abdominal) fat fell by 15.2% with tesamorelin and rose by 5.0% with placebo [6]. A pooled analysis of two phase 3 trials with 806 patients found that the reduction was maintained for up to 52 weeks in those who continued treatment [4], and a review found that the fat came back after treatment stopped [7]. Reviewers found only limited data supporting uses beyond HIV-associated fat accumulation [8], and a 2026 review for sports-medicine physicians found no orthopedic evidence for tesamorelin [10].

Sermorelin’s human data are older and mostly in children. It was used as a diagnostic test for growth hormone deficiency and, based on limited data, to treat some children with idiopathic growth hormone deficiency [1]. The 1999 review noted that the recommended sermorelin regimen hadn’t been compared directly with somatropin (growth hormone itself), and that growth gains with some other ways of giving sermorelin were smaller than with somatropin [1]. In adults, a 2020 review of growth hormone secretagogues, sermorelin among them, found clinical data on men with low testosterone largely lacking [9].

Regulation and sport

Today tesamorelin is an approved prescription medicine in the US [5], while sermorelin’s products were discontinued in 2008 and FDA withdrew both approvals effective June 18, 2009 [2]. WADA prohibits both at all times as growth hormone-releasing hormone analogues [11].

Quality risks when buying

In the US, Egrifta is available only on prescription [5]. Vials sold as research-grade tesamorelin or sermorelin come from unregulated supply chains, where a 2026 review notes uncertain quality and composition [13]. Anti-doping laboratories testing black-market growth-promoting products have found modified versions of known peptides, identified using high-resolution mass spectrometry [12].

So a batch certificate of analysis (COA) should confirm the molecule’s identity by mass spectrometry and give a measured purity, not just a label claim. Our guides explain how to read a COA, how to check a vendor and what “research use only” means.

For more detail, see our sermorelin overview and tesamorelin overview, and today’s prices for sermorelin and tesamorelin. Related comparisons: CJC-1295 vs sermorelin and ipamorelin vs sermorelin.

Frequently asked questions

What is the difference between sermorelin and tesamorelin?

Both are versions of growth hormone-releasing hormone (GHRH). Sermorelin is a 29-amino-acid fragment with the hormone's full activity. Tesamorelin is the full 44-amino-acid hormone with a chemical group added that slows its breakdown. Tesamorelin is a current US prescription medicine for HIV-associated abdominal fat; sermorelin's US products, sold as Geref, were discontinued in 2008.

Is sermorelin FDA-approved?

It was, as Geref, approved in 1990 and 1997. Both products were discontinued in 2008, and FDA determined in 2013 that they were not withdrawn for reasons of safety or effectiveness.

Is research-grade tesamorelin the same as Egrifta?

No. Egrifta is the FDA-approved prescription medicine. Vials sold as research tesamorelin are not Egrifta and haven't been reviewed by any regulator.

Sources

  1. Sermorelin: a review of its use in the diagnosis and treatment of children with idiopathic growth hormone deficiency. BioDrugs (1999). Accessed Oct 15, 2026
  2. Determination That GEREF (Sermorelin Acetate) Injection ... Were Not Withdrawn From Sale for Reasons of Safety or Effectiveness (78 FR 14095, 4 March 2013). U.S. Food and Drug Administration, Federal Register. Accessed Oct 15, 2026
  3. Non-clinical pharmacology and safety evaluation of TH9507, a human growth hormone-releasing factor analogue. Basic & Clinical Pharmacology & Toxicology (2007). Accessed Oct 15, 2026
  4. Effects of tesamorelin (TH9507), a growth hormone-releasing factor analog, in HIV-infected patients with excess abdominal fat: a pooled analysis of two phase 3 trials with safety extension data. Journal of Clinical Endocrinology & Metabolism (2010). Accessed Oct 15, 2026
  5. Drugs@FDA: application 022505 (Egrifta), original approval 10 November 2010. U.S. Food and Drug Administration. Accessed Oct 15, 2026
  6. Metabolic effects of a growth hormone-releasing factor in patients with HIV. New England Journal of Medicine (2007). Accessed Oct 15, 2026
  7. Tesamorelin: a review of its use in the management of HIV-associated lipodystrophy. Drugs (2011). Accessed Oct 15, 2026
  8. Tesamorelin: a growth hormone-releasing factor analogue for HIV-associated lipodystrophy. Annals of Pharmacotherapy (2012). Accessed Oct 15, 2026
  9. Beyond the androgen receptor: the role of growth hormone secretagogues in the modern management of body composition in hypogonadal males. Translational Andrology and Urology (2020). Accessed Oct 15, 2026
  10. Injectable Peptide Therapy: A Primer for Orthopaedic and Sports Medicine Physicians. American Journal of Sports Medicine (2026). Accessed Oct 15, 2026
  11. World Anti-Doping Code International Standard: Prohibited List 2026 (in force 1 January 2026). World Anti-Doping Agency. Accessed Oct 15, 2026
  12. Analysis of new growth promoting black market products. Growth Hormone & IGF Research (2018). Accessed Oct 15, 2026
  13. The emerging landscape of performance-enhancing peptides modulating GH-IGF1 axis: bridging the gap between clinical evidence and patient self-administration (full text). Frontiers in Endocrinology (2026). Accessed Oct 15, 2026
  14. Drugs@FDA: NDA 019863 (Geref), original approval 28 December 1990, discontinued. U.S. Food and Drug Administration. Accessed Oct 14, 2026
  15. Drugs@FDA: NDA 020443 (Geref), original approval 26 September 1997, discontinued. U.S. Food and Drug Administration. Accessed Oct 14, 2026
  16. MHRA Products: licensed-medicine search for "sermorelin". Medicines and Healthcare products Regulatory Agency (UK). Accessed Oct 14, 2026
  17. EMA medicines data: centrally authorised human medicines (export of 14 October 2026). European Medicines Agency. Accessed Oct 14, 2026
  18. EMA Article 57 product data: medicines authorised in the EU/EEA (data as of 9 October 2026). European Medicines Agency. Accessed Oct 14, 2026
  19. Drug Product Database online query (searched by active ingredient). Health Canada. Accessed Oct 14, 2026
  20. Therapeutic Goods (Poisons Standard—October 2026) Instrument 2026 (F2026L01327, registered 30 September 2026). Federal Register of Legislation, Australian Government. Accessed Oct 14, 2026
  21. Safety and Efficacy of Approved and Unapproved Peptide Therapies for Musculoskeletal Injuries and Athletic Performance. Sports Medicine (2026). Accessed Oct 14, 2026
  22. MHRA Products: licensed-medicine search for "tesamorelin". Medicines and Healthcare products Regulatory Agency (UK). Accessed Oct 14, 2026
  23. Egrifta: withdrawn application (withdrawn 21 June 2012). European Medicines Agency. Accessed Oct 14, 2026
  24. Drug Product Database: Egrifta, status Cancelled Post Market. Health Canada. Accessed Oct 14, 2026
  25. Identification of black market products and potential doping agents in Germany 2010-2013. European Journal of Clinical Pharmacology (2014). Accessed Oct 14, 2026