CJC-1295 / Ipamorelin

$28.00

CJC-1295 (No DAC) / Ipamorelin is a dual-pathway growth hormone secretagogue blend studied for natural GH pulse signaling, IGF-1 pathways, recovery biology, body-composition research, and pituitary-axis activity. It combines a GHRH analog with a selective ghrelin-receptor agonist for a broader research model than either compound alone.

Volume Pricing

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QuantityPricing
1–3 vialsStandard price
4–6 vialsSave 3%
7–9 vialsSave 6%
10+ vialsSave 10%

Quantity tiers apply separately to each selected strength or formulation.

SKU: CJCIPA Category: Tags: , , , ,

Product Overview

CJC-1295 (No DAC), more accurately described as Modified GRF (1-29), targets the growth hormone-releasing hormone pathway. Ipamorelin works through the ghrelin receptor as a selective growth hormone secretagogue. Together, they allow researchers to examine complementary signals involved in endogenous GH release.

The blend is commonly associated with research involving pulsatile growth-hormone signaling, downstream IGF-1 activity, recovery and tissue-remodeling pathways, metabolic regulation, and body-composition models. The No DAC formulation is especially relevant where shorter-acting GHRH signaling is preferred over the extended exposure associated with DAC-containing CJC-1295.

Included Compounds

  • CJC-1295 (No DAC) — Modified GRF (1–29)
  • Ipamorelin

Common Research Areas

⦁ Growth hormone pulse signaling
⦁ Pituitary and ghrelin-receptor pathways
⦁ IGF-1 pathway research
⦁ Recovery and tissue-remodeling models
⦁ Metabolic and body-composition research

Research References

  1. CJC-1295-Related Research References (Note: Some citations examine DAC-containing CJC-1295, which exhibits a significantly extended half-life compared to the No DAC variant. Findings related to DAC-containing formulations should not be assumed to be equivalent to the No DAC material.)
  2. Teichman SL, et al. “Prolonged pharmacokinetics and pharmacodynamics of CJC-1295, a long-acting growth hormone-releasing hormone analogue.” Journal of Clinical Endocrinology and Metabolism. 2006;91(3):795–801. DOI: 10.1210/jc.2005-1536.
  3. Teichman SL, et al. “Safety and tolerability of a drug affinity complex growth hormone-releasing hormone analogue in healthy subjects.” Journal of Clinical Endocrinology and Metabolism. 2006;91(7):2602–2608. DOI: 10.1210/jc.2005-2533.
Dimensions N/A
Blend Strength

5 mg / 5 mg

Formulation Type

Blend

Compound

,

Supplied Form

Lyophilized

Container

3 mL vial