CJC-1295 & Ipamorelin Blend



$105.00

  • GH pulsatility enhancement (GHRH + GHS synergy)

  • Lean‑mass support & body‑composition improvements

  • Musculoskeletal recovery & connective‑tissue support

  • Bone metabolism & osteoblastic activity

  • Metabolic flexibility & lipid regulation

  • Age‑related GH/IGF‑1 decline

  • Sleep quality & circadian rhythm support

CJC‑1295 (without DAC)

  • Stimulates GHRH receptors in the pituitary

  • Enhances physiologic GH pulsatility

  • Supports IGF‑1 elevation through natural GH signaling

  • Avoids continuous GH elevation associated with exogenous GH therapy

Ipamorelin

  • Selectively activates GHS‑R1a (ghrelin receptor)

  • Triggers GH release with minimal cortisol, prolactin, or ACTH impact

  • Supports recovery, lean‑mass development, and neuroendocrine balance

Combined Effect

  • Dual stimulation of GH axis (GHRH + GHS synergy)

  • Amplified physiologic GH pulses

  • More natural IGF‑1 elevation

  • Reduced endocrine spillover compared to older secretagogues

 

This blend is composed of research‑grade peptides and is not FDA‑approved for therapeutic, anti‑aging, or performance use. Most available data come from preclinical studies and early‑stage research. Even so, the combination has gained significant interest in wellness, performance, and endocrine‑focused research communities, supported by substantial anecdotal reporting. While more large‑scale studies are needed, the blend’s dual‑pathway selectivity and promising early findings continue to drive scientific and community interest in GH‑modulating peptide research.

1. Teichman, S. L., Neale, A., Lawrence, B., Gagnon, C., Castaigne, J. P., & Frohman, L. A. (2006). Prolonged stimulation of growth hormone (GH) and insulin‑like growth factor‑I (IGF‑I) secretion by CJC‑1295, a long‑acting GH‑releasing hormone analog. Journal of Clinical Endocrinology & Metabolism, 91(3), 799–805.
2. Castaigne, J. P., et al. (2004). Pharmacodynamic effects of CJC‑1295, a long‑acting GHRH analog, in healthy adults. Clinical Pharmacology & Therapeutics, 76(3), 217–227.
3. Raun, K., Hansen, B. S., Johansen, N. L., Thøgersen, H., Madsen, K., & Thim, L. (1998). Ipamorelin, the first selective growth hormone secretagogue. European Journal of Endocrinology, 139(5), 552–561.
4. Raun, K., et al. (1999). Pharmacological profile of Ipamorelin: selective GH release without effects on prolactin or cortisol. Journal of Endocrinology, 161(3), 481–489.
5. Johansen, N. L., et al. (1997). Design and development of selective GH secretagogues: the Ipamorelin model. Peptides, 18(9), 1265–1271.


full product description

A CJC‑1295 + Ipamorelin blend combines two complementary growth hormone–modulating peptides:

  • CJC‑1295 (without DAC) — a long‑acting GHRH analog that enhances physiologic pulsatile GH release and increases IGF‑1 via pituitary stimulation.
  • Ipamorelin — a highly selective growth hormone secretagogue (GHS) and ghrelin receptor agonist (GHS‑R1a) that triggers GH release with minimal impact on cortisol, prolactin, or ACTH.

 

Together, these peptides target two distinct but convergent regulatory nodes of the GH axis: hypothalamic GHRH signaling (CJC‑1295) and ghrelin‑mediated pituitary stimulation (Ipamorelin). This dual approach is designed to amplify physiologic GH pulsatility, support IGF‑1 elevation within a more natural rhythm, and minimize the endocrine “spillover” seen with older GHS compounds. Both remain research peptides (outside specific clinical contexts) and are not broadly FDA‑approved for anti‑aging or performance indications.

A CJC‑1295 + Ipamorelin blend leverages dual GH‑axis stimulation—GHRH and ghrelin pathways—to enhance physiologic GH pulsatility and IGF‑1 levels, supporting body composition, recovery, and metabolic research with a more selective endocrine profile than older secretagogues.

QUANTITY: 10 MG (5 MG CJC-1295 + 5 MG IPAMORELIN)



Join Waitlist We will inform you when the product arrives in stock. Please leave your valid email address below.