Research Reference · Growth-Hormone Axis
CJC-1295
A long-acting growth-hormone-releasing hormone (GHRH) analogue studied for sustained growth-hormone and IGF-1 release, often discussed with Ipamorelin.
At a glance
CJC-1295 is a lab-made analogue of growth-hormone-releasing hormone built to last far longer than the natural hormone. In its best-known form (“with DAC”) it attaches to albumin in the blood; in healthy adults its half-life was about six to eight days. Research focuses on growth hormone and IGF-1 levels. Evidence comes from animal studies and early human studies.
What it’s studied for
Long-acting GH release
Sustained, dose-dependent rises in growth hormone and IGF-1 in healthy adults. 2
HumanNatural GH pulses
Growth hormone was still released in pulses during continuous stimulation. 3
HumanGrowth in GHRH-deficient mice
Once-daily treatment normalized growth and body composition in knockout mice. 4
AnimalNot currently stocked
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How it works
CJC-1295 is based on the first 29 amino acids of human GHRH — the part that carries its activity — with changes that protect it from breakdown and a “drug affinity complex” (DAC) that lets it bind to albumin in the blood. In rats this produced a stable, active GHRH analogue with an extended plasma half-life. 1
In healthy adults, CJC-1295 produced sustained, dose-dependent increases in growth hormone and IGF-1, with a half-life of 5.8–8.1 days; after repeated administration IGF-1 stayed above baseline for up to 28 days. 2 Growth hormone continued to be released in pulses rather than continuously. 3
Suppliers also use the name for a version without DAC, and public database records for the two forms are inconsistent, so check which form a certificate of analysis describes.
Related research
Frequently asked questions
What is DAC?
How long does CJC-1295 last?
How is CJC-1295 different from Ipamorelin?
Has CJC-1295 been studied in humans?
Do you sell CJC-1295?
Identifiers
| Name | CJC-1295 |
|---|---|
| Class | GHRH analogue based on hGRF(1-29) |
| Form in the key human studies | With DAC (albumin-binding) |
| PubChem “CJC-1295” record | CID 91971820 · CAS 446262-90-4 |
| Status | Investigational — not an approved drug |
Checked against PubChem. PubChem’s records for the DAC and non-DAC forms are inconsistent, so no single molecular formula is listed here.
Research timeline
Key studies
| Study | Model | What it found |
|---|---|---|
| Jetté 2005 1 | Rat | Bound serum albumin and stayed active with an extended plasma half-life. |
| Teichman 2006 2 | Human · healthy adults | Sustained, dose-dependent GH and IGF-1 increases; half-life 5.8–8.1 days. |
| Ionescu 2006 3 | Human | Raised trough and mean GH and IGF-1 while preserving GH pulsatility. |
| Alba 2006 4 | Mouse | Once-daily treatment maintained normal growth and body composition in GHRH-knockout mice. |
| Sackmann-Sala 2009 5 | Human | Serum protein changes proposed as biomarkers of GH/IGF-1 action. |
Sources
- 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. Endocrinology, 2005.
- 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. J Clin Endocrinol Metab, 2006. Human
- Pulsatile secretion of growth hormone (GH) persists during continuous stimulation by CJC-1295, a long-acting GH-releasing hormone analog. Ionescu M, Frohman LA. J Clin Endocrinol Metab, 2006. Human
- 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. Am J Physiol Endocrinol Metab, 2006.
- 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 Horm IGF Res, 2009. Free full textHuman
Last reviewed September 2026 by Midwest Compounds. Every source above was checked against its original publication.