CJC-1295 vs Sermorelin: Differences, Evidence and Status

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

CJC-1295 with DAC vs Sermorelin at a glance

FactCJC-1295 with DACSermorelin
Also known asCJC 1295, CJC-1295 DAC, CJC-1295 with Drug Affinity ComplexGRF (1-29), Geref, Sermorelin acetate
What it isSynthetic long-acting GHRH analogue with a drug affinity complex (DAC)Synthetic GHRH(1-29) analogue (formerly approved in the US)
Evidence levelEarly human trialsFormerly approved drug (approvals withdrawn)
Approved productsNoneGeref (discontinued) (US, 1990); Geref (discontinued) (US, 1997)
United StatesNot FDA-approved; the nomination of CJC-1295 for pharmacy (503A) compounding was withdrawn after FDA flagged potential safety risks [11][6].Approved by the FDA as Geref in 1990 and 1997; both products were discontinued in 2008, and FDA withdrew both approvals effective June 18, 2009 [20][21][5].
United KingdomNo UK-licensed medicine containing CJC-1295 appears in the MHRA products database [12].No UK-licensed medicine containing sermorelin appears in the MHRA products database [22].
European UnionNo medicine containing CJC-1295 is authorized in the EU, according to EMA's central and Article 57 product data [13][14].No medicine containing sermorelin is authorized in the EU, according to EMA's central and Article 57 product data [13][14].
CanadaNo product containing CJC-1295 appears in Health Canada's Drug Product Database [15].No product containing sermorelin appears in Health Canada's Drug Product Database [15].
AustraliaSchedule 4 (prescription-only) in Australia's Poisons Standard, with possession without authority prohibited under Appendix D [16].Schedule 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) [16].
Sport (WADA)Named as a prohibited growth hormone-releasing hormone analogue under S2 [8].Named as a prohibited growth hormone-releasing hormone analogue under S2 [8].
Vendors we track31 vendors62 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.

CJC-1295 and sermorelin are both built on the same active part of growth hormone-releasing hormone (GHRH): its first 29 amino acids [1, 2, 4]. Sermorelin stays close to that natural fragment and is short-acting [1, 4]. CJC-1295 has four amino acids swapped and an added chemical group, the drug affinity complex (DAC), that binds it to albumin in the blood, so a single administration acts for days [2, 3, 4]. Sermorelin was once an FDA-approved drug [5]; CJC-1295 is not approved by major regulators such as FDA and EMA, and its published human data are limited to early studies in healthy adults [4].

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), with a disappearance half-time of about four minutes [4].

CJC-1295 starts from the same 29 amino acids but swaps four of them, which makes it more resistant to breakdown by enzymes [2, 4]. It also carries an extra lysine at the end with a maleimide group attached [2]. That group bonds to serum albumin: in rats, CJC-1295 was still present in plasma beyond 72 hours [2]. This is the DAC, and it’s why the molecule lasts so much longer [4].

Many vendors also sell a version without the DAC, labeled “CJC-1295 without DAC” or “Mod GRF 1-29” [4]. It’s a different molecule with different evidence: see our comparison of CJC-1295 with and without DAC.

How the evidence compares

CJC-1295. Its main human data come from two small randomized, placebo-controlled trials in healthy adults, published in 2006, which measured how the body handles it, its effect on hormone levels and its safety [3]. The authors introduced it by noting that the short duration of action of GHRH limits its use [3]. Growth hormone levels rose 2- to 10-fold for six days or more, IGF-I levels rose 1.5- to 3-fold for 9 to 11 days, the estimated half-life was 5.8 to 8.1 days, and no serious adverse reactions were reported in those trials [3]. A 2026 review classes this as phase I evidence with no controlled efficacy data [4].

Sermorelin. 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]. In adults, a 2020 review of growth hormone secretagogues found clinical data on men with low testosterone largely lacking [7].

A 2026 sports-medicine review lists both among the peptides marketed directly to patients for injury recovery and athletic performance, and notes that rigorous human safety data for unapproved peptides are scarce [10].

Regulation and sport

FDA approved sermorelin as Geref in 1990 and 1997; both products were discontinued in 2008, not for reasons of safety or effectiveness, according to FDA [5]. CJC-1295 is not approved by major regulators [4], FDA has identified serious adverse events associated with it, including increased heart rate and a systemic vasodilatory reaction [6], and WADA prohibits both at all times as GHRH analogues [8].

Quality risks when buying

Research-grade vials of either come from unregulated supply chains [4]. FDA warns that compounded CJC-1295 may cause immune reactions and has complexities with peptide-related impurities and characterization [6].

Labels can also be wrong about which molecule is in the vial. In 2009, a laboratory analyzing seized products for Norwegian police and customs found a 29-amino-acid peptide consistent with one then marketed as CJC-1295 [9], without the extra lysine and DAC described in the original research [2]. A certificate of analysis (COA) should name the exact molecule, with or without DAC, and confirm it by mass spectrometry. Our guides explain how to read a COA, how to check a vendor and what “research use only” means.

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

Frequently asked questions

What is the difference between CJC-1295 and sermorelin?

Both are based on the first 29 amino acids of growth hormone-releasing hormone. Sermorelin stays close to that natural fragment and is short-acting. CJC-1295 has four amino acids swapped and a drug affinity complex (DAC) that binds it to albumin in the blood, so its effects last for days.

Is CJC-1295 FDA-approved?

No. Its main published human data come from two small early-stage trials in healthy adults, and it isn't approved. FDA has identified serious adverse events associated with it, including increased heart rate.

Was sermorelin ever approved?

Yes. FDA approved it as Geref 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.

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. Human growth hormone-releasing factor (hGRF)1-29-albumin bioconjugates activate the GRF receptor on the anterior pituitary in rats: identification of CJC-1295 as a long-lasting GRF analog. Endocrinology (2005). Accessed Oct 15, 2026
  3. Prolonged stimulation of GH and IGF-I secretion by CJC-1295, a long-acting analog of GH-releasing hormone, in healthy adults. Journal of Clinical Endocrinology & Metabolism (2006). Accessed Oct 15, 2026
  4. 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
  5. 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
  6. Certain Bulk Drug Substances for Use in Compounding that May Present Significant Safety Risks (content current as of 22 April 2026). U.S. Food and Drug Administration. Accessed Oct 15, 2026
  7. 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
  8. World Anti-Doping Code International Standard: Prohibited List 2026 (in force 1 January 2026). World Anti-Doping Agency. Accessed Oct 15, 2026
  9. Identification of CJC-1295, a growth-hormone-releasing peptide, in an unknown pharmaceutical preparation. Drug Testing and Analysis (2010). Accessed Oct 15, 2026
  10. Safety and Efficacy of Approved and Unapproved Peptide Therapies for Musculoskeletal Injuries and Athletic Performance. Sports Medicine (2026). Accessed Oct 15, 2026
  11. Drugs@FDA: FDA-Approved Drugs (database searched by active ingredient). U.S. Food and Drug Administration. Accessed Oct 14, 2026
  12. MHRA Products: licensed-medicine search for "cjc-1295". Medicines and Healthcare products Regulatory Agency (UK). Accessed Oct 14, 2026
  13. EMA medicines data: centrally authorised human medicines (export of 14 October 2026). European Medicines Agency. Accessed Oct 14, 2026
  14. EMA Article 57 product data: medicines authorised in the EU/EEA (data as of 9 October 2026). European Medicines Agency. Accessed Oct 14, 2026
  15. Drug Product Database online query (searched by active ingredient). Health Canada. Accessed Oct 14, 2026
  16. Therapeutic Goods (Poisons Standard—October 2026) Instrument 2026 (F2026L01327, registered 30 September 2026). Federal Register of Legislation, Australian Government. Accessed Oct 14, 2026
  17. Injectable Peptide Therapy: A Primer for Orthopaedic and Sports Medicine Physicians. American Journal of Sports Medicine (2026). Accessed Oct 14, 2026
  18. Analysis of new growth promoting black market products. Growth Hormone & IGF Research (2018). Accessed Oct 14, 2026
  19. Identification of a novel growth hormone releasing peptide (a glycine analogue of GHRP-2) in a seized injection vial. Drug Testing and Analysis (2019). Accessed Oct 14, 2026
  20. Drugs@FDA: NDA 019863 (Geref), original approval 28 December 1990, discontinued. U.S. Food and Drug Administration. Accessed Oct 14, 2026
  21. Drugs@FDA: NDA 020443 (Geref), original approval 26 September 1997, discontinued. U.S. Food and Drug Administration. Accessed Oct 14, 2026
  22. MHRA Products: licensed-medicine search for "sermorelin". Medicines and Healthcare products Regulatory Agency (UK). Accessed Oct 14, 2026