CJC-1295 + Ipamorelin
A combined research blend of CJC-1295 (a GHRH analog) and Ipamorelin (a selective GHRP), studied for synergistic growth-hormone axis signalling and pulsatile release patterns.
⏱ Half-Life
Moderate–Long duration profile
CJC-1295 + Ipamorelin demonstrates a moderate–long half-life characteristic in research literature, shaping how observation windows and study timelines are typically structured.
⚡ Onset Characteristics
Gradual measurable response
Onset is observed as gradual — a property that influences how researchers structure comparative studies versus other compounds in the signalling research category.
🧠 Key Notes
What makes it distinct
- 01Combines a GHRH analog with a selective GHRP for additive signalling
- 02Ipamorelin is studied for its selective profile vs other GHRPs
- 03Frequently referenced in long-duration endocrine research
🧬 Mechanism of Action
How it works
CJC-1295 (without DAC) is a stabilised analog of growth-hormone-releasing hormone (GHRH) that binds the pituitary GHRH receptor to amplify natural GH pulses. Ipamorelin is a selective ghrelin/GH-secretagogue receptor (GHS-R) agonist that triggers GH release through a complementary pathway. Used together, they act on two separate receptors in the somatotroph cells, producing a synergistic GH pulse that is larger than either compound alone but still preserves the body's natural pulsatile rhythm. Critically, Ipamorelin is highly selective — it does not meaningfully stimulate cortisol or prolactin release, isolating the GH-axis effect.
✨ Documented Benefits
What the research shows it supports
🔍 Research Insights
What the literature shows
The two molecules act on complementary receptors — GHRH and ghrelin — producing a synergistic, more physiologic GH pulse than either alone.
Ipamorelin's selectivity means minimal cortisol or prolactin elevation in research, isolating GH-axis effects.
CJC-1295 (without DAC) preserves the body's natural pulsatile release pattern, unlike its longer-acting DAC counterpart.
🧪 Typical Research Use Cases
Where it appears in study design
Pulsatile growth-hormone axis research.
Recovery and lean-mass composition modelling.
Comparative endocrine studies vs Tesamorelin.
📚 References
Peer-reviewed literature
Primary research sources cited on this profile. All links resolve to PubMed or the publishing journal.
- [01]
Teichman, S. L. et al. (2006). 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. Journal of Clinical Endocrinology & Metabolism, 91(3), 799–805.
J Clin Endocrinol Metab ↗ - [02]
Raun, K. et al. (1998). Ipamorelin, the first selective growth hormone secretagogue. European Journal of Endocrinology, 139(5), 552–561.
European Journal of Endocrinology ↗ - [03]
Sinha, D. K. et al. (2020). Beyond the androgen receptor: the role of growth hormone secretagogues in the modern management of body composition in hypogonadal males. Translational Andrology and Urology, 9(Suppl 2), S149–S159.
Translational Andrology and Urology ↗ - [04]
Alba, M. et al. (2006). Once-daily administration of CJC-1295, a long-acting growth hormone-releasing hormone (GHRH) analog, normalizes growth in the GHRH knockout mouse. American Journal of Physiology — Endocrinology and Metabolism, 291(6), E1290–E1294.
Am J Physiol Endocrinol Metab ↗
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