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For Research & Educational Discussion Only. Not Medical Advice

CJC-1295

Growth hormone-releasing hormone (GHRH) analogue

Also known as Modified GRF (1-29), CJC-1295 DAC, Sermorelin analogue

A GHRH analogue with early human pharmacokinetic data and no efficacy programme. The DAC and non-DAC versions are pharmacologically very different and are constantly conflated.

Guide updated Sep 2, 2026Literature checked Sep 2, 20261 curated study19 literature recordsBaseline editorial

Overview

In shortTwo different things are sold under this one name and they are not interchangeable. The version with DAC sticks to a blood protein and lasts about a week. The version without it lasts minutes. Those are different drugs with different risk profiles, and treating a study of one as evidence about the other shows up in almost every discussion of it.

CJC-1295 is a modified fragment of growth hormone-releasing hormone. Two distinct things are sold under the name and they are not interchangeable.

CJC-1295 with DAC carries a Drug Affinity Complex that binds serum albumin, extending its half-life from minutes to something on the order of a week. CJC-1295 without DAC, properly modified GRF (1-29), has a half-life measured in minutes.

Those are different drugs with different exposure profiles and different plausible risk profiles, and treating a citation about one as evidence about the other is a category error that shows up in almost every discussion of it.

Mechanism

In shortBoth versions tell the pituitary to release your own growth hormone, keeping the body's normal feedback intact in a way that injecting growth hormone does not. The DAC version changes things fundamentally: instead of a bigger pulse you get a permanently raised level. Growth hormone normally comes in pulses and some effects depend on that pattern, so a constant level is not just more of the same.

Both versions bind the GHRH receptor on pituitary somatotrophs and stimulate endogenous growth hormone release, preserving pituitary feedback in a way exogenous GH does not.

The DAC modification changes the pharmacology fundamentally rather than incrementally: sustained receptor exposure produces a raised GH and IGF-1 baseline rather than an amplified pulse. Since GH signalling is normally pulsatile and downstream effects are partly pattern-dependent, a sustained elevation is not simply "more of the same".

Evidence

In shortOnly early studies of how it behaves in the body, and no properly sized trial of any actual outcome. The human work shows it raises growth hormone and IGF-1, with the DAC version keeping them up for days. That is a measurement, not a result. Raises growth hormone, therefore does X, skips the step that testing exists to check.

Early clinical pharmacokinetics only. There is no adequately powered efficacy trial for any clinical outcome.

The published human work establishes that it raises GH and IGF-1 in a dose-dependent, sustained way. The DAC version producing elevations lasting days. That is a pharmacodynamic result, not a clinical one.

For body composition, recovery, sleep quality, injury healing, or anything else discussed in community settings, there is no controlled human evidence. The reasoning chain, raises GH, therefore raises IGF-1, therefore produces outcome X, skips the step that pharmacology exists to test.

Safety

In shortHuman exposure is limited to small, short studies reporting injection site reactions, flushing and headache. The concerns come from keeping growth hormone and IGF-1 raised: insulin resistance, fluid retention, joint pain, and cell-growth implications. Because both versions share a name, buyers often do not know which one they have.

Human exposure is limited to small short-duration studies. Reported effects include injection site reactions, flushing, and headache.

The mechanistic concerns are those of sustained GH/IGF-1 elevation: insulin resistance and impaired glucose tolerance, fluid retention, arthralgia, and the mitogenic implications of chronic IGF-1 elevation. The DAC version's sustained profile makes these more relevant, not less, and no long-term data exists for it.

An additional practical issue specific to this compound: because both versions are sold under one name, buyers frequently do not know which molecule they have.

Regulatory status

In shortNever approved anywhere. Sold as a research chemical, banned in sport, and not made to medicine standards outside a research setting.

Never approved anywhere. Sold as a research chemical. Prohibited in sport under WADA's S2 category. Not manufactured to pharmaceutical standards outside a research setting.

The literature

1 study indexed. Findings and limitations get equal weight, on purpose.

Always check the primary source

Members area

The CJC-1295 literature needs an account

Everything above is free to read. What an account opens is the evidence underneath it: 1 study with their limitations, and the regimen each trial actually reported.

  • Every study, with what it found and what it cannot show
  • The limitations, given the same weight as the findings
  • The dose each named trial administered, where recorded

Free to create. A membership is separate, and you can decide about that later.

Reading is free, an account is not the same as paying. 43 compound guides, every study with its limitations written underneath, and the regimens those trials actually used. A free account opens all of it. A membership is a separate decision, and it opens the forum. What membership costs.

The wider literature

19 indexed papers and 0 registered trials mentioning CJC-1295, straight from PubMed and ClinicalTrials.gov. These have not been read by us. Unlike the studies above, they carry no findings and no limitations written by anyone here, because writing either would mean claiming a reading nobody has done. They are a starting point for yours.

Papers (19)

  1. Peptide Supplements and Their Therapeutic Applications in Sports Medicine.

    Tewari K, et al.The American journal of sports medicine2026PMID 42578445

    journal article

  2. Injectable Peptide Therapy: A Primer for Orthopaedic and Sports Medicine Physicians.

    Mayfield CK, et al.The American journal of sports medicine2026PMID 41476424

    journal articlereview

  3. Therapeutic Peptides in Orthopaedics: Applications, Challenges, and Future Directions.

    Rahman OF, et al.Journal of the American Academy of Orthopaedic Surgeons. Global research & reviews2026PMID 41490200

    journal articlereview

  4. A new era of doping? Use of peptide and peptide-analog drugs in recreational and professional sport and bodybuilding: a critical review.

    Coutinho LFD, et al.The Journal of sports medicine and physical fitness2026PMID 41880199

    journal articlereview

  5. Therapeutic Peptides in Aesthetic, Metabolic and Endocrine Conditions: Effects, Safety, Clinical Applications, and Future Perspectives.

    Renke G, et al.International journal of molecular sciences2026PMID 42123471

    journal articlereview

  6. Therapeutic peptides in gerontology: mechanisms and applications for healthy aging.

    Mavrych V, et al.Frontiers in aging2026PMID 42021992

    journal articlereview

  7. Injectable Peptides in Sports Medicine: A Structured Narrative Review of Evidence, Safety, and Antidoping Implications.

    Villegas Meza AD, et al.JBJS reviews2026PMID 42160466

    journal articlereview

  8. Safety and Efficacy of Approved and Unapproved Peptide Therapies for Musculoskeletal Injuries and Athletic Performance.

    Mendias CL, et al.Sports medicine (Auckland, N.Z.)2026PMID 41966639

    journal articlereview

  9. Analysis of growth hormone releasing hormone and its analogs in urine using nano liquid chromatography coupled with quadrupole/orbitrap mass spectrometry.

    Uçaktürk E, et al.Journal of pharmaceutical and biomedical analysis2026PMID 41138283

    journal article

  10. Cationic exchange SPE combined with triple quadrupole UHPLC-MS/MS for detection of GHRHs in urine samples.

    Cristea CD, et al.Analytical biochemistry2023PMID 37806509

    journal articleresearch support, non-u.s. gov't

  11. Probing for peptidic drugs (2-10 kDa) in doping control blood samples.

    Thomas A, et al.Analytical science advances2022PMID 38716080

    journal article

  12. Advances in the detection of growth hormone releasing hormone synthetic analogs.

    Memdouh S, et al.Drug testing and analysis2021PMID 34665524

    journal articlevalidation study

  13. Comparison of magnetic bead surface functionalities for the immunopurification of growth hormone-releasing hormones prior to liquid chromatography-high resolution mass spectrometry.

    Pont L, et al.Journal of chromatography. A2020PMID 32971474

    journal article

  14. A method for confirming CJC-1295 abuse in equine plasma samples by LC-MS/MS.

    Timms M, et al.Drug testing and analysis2019PMID 30938069

    journal articlevalidation study

  15. Netnography of Female Use of the Synthetic Growth Hormone CJC-1295: Pulses and Potions.

    Van Hout MC, et al.Substance use & misuse2016PMID 26771670

    journal articlereview

  16. Activation of the GH/IGF-1 axis by CJC-1295, a long-acting GHRH analog, results in serum protein profile changes in normal adult subjects.

    Sackmann-Sala L, et al.Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society2009PMID 19386527

    journal articleresearch support, n.i.h., extramuralresearch support, non-u.s. gov't

  17. Once-daily administration of CJC-1295, a long-acting growth hormone-releasing hormone (GHRH) analog, normalizes growth in the GHRH knockout mouse.

    Alba M, et al.American journal of physiology. Endocrinology and metabolism2006PMID 16822960

    journal article

  18. Prolonged stimulation of growth hormone (GH) and insulin-like growth factor I secretion by CJC-1295, a long-acting analog of GH-releasing hormone, in healthy adults.

    Teichman SL, et al.The Journal of clinical endocrinology and metabolism2006PMID 16352683

    journal articlerandomized controlled trialresearch support, non-u.s. gov't

  19. 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.

    Jetté L, et al.Endocrinology2005PMID 15817669

    journal article

Discussion

CJC-1295 has its own forum, split by the same six categories as the rest of the site.

14 papers on CJC-1295, zero trials that administered it

CJC 1295 is a Growth hormone releasing hormone (GHRH) analogue, and the guide for it is up.…

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For Research & Educational Discussion Only. Not Medical Advice

This guide is educational reference material compiled from published literature. It is not medical advice, not a recommendation, and not a substitute for a clinician who knows your history. Nothing here should be used to make a decision about your own health without one.

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