CJC-1295 (DAC)
Medium EvidenceA long-acting GHRH analog with an extended half-life due to its Drug Affinity Complex modification.
What It Is
CJC-1295 with DAC (Drug Affinity Complex) is a synthetic GHRH analog that incorporates a maleimidopropionic acid linker enabling covalent binding to circulating albumin. This DAC modification extends the peptide's half-life from approximately 30 minutes (no-DAC) to 6–8 days, producing sustained GH and IGF-1 elevation rather than the pulsatile release pattern of the no-DAC version. In clinical studies, a single subcutaneous injection of CJC-1295 DAC increased mean GH concentrations by 2- to 10-fold for up to 6 days and raised IGF-1 levels by 1.5- to 3-fold for 9–11 days. A Phase II trial enrolling 56 healthy subjects confirmed dose-dependent, sustained elevations in both GH and IGF-1 with once-weekly dosing. The sustained GH elevation produced by the DAC formulation differs fundamentally from natural GH physiology, which relies on discrete pulsatile secretion. This non-pulsatile pattern has raised concerns about potential desensitization of GH receptors and disruption of the normal GH feedback axis with chronic use. Researchers who prefer physiological GH pulsatility typically favor the no-DAC version combined with ipamorelin. CJC-1295 DAC was placed on the FDA's Category 2 list in October 2023. As of May 2026, it remains restricted for 503B outsourcing facilities, though the 503A compounding nomination has been withdrawn. It is classified as a prohibited substance by WADA and is not FDA-approved for any indication.
Why Researchers Study It
CJC-1295 with DAC provides a sustained, non-pulsatile elevation of GH and IGF-1 over days rather than hours. This pharmacokinetic profile makes it a useful research tool for studying the effects of chronic GH elevation versus the pulsatile release pattern produced by the no-DAC variant.
Proposed Mechanisms
- Drug Affinity Complex binds serum albumin, extending half-life to 6–8 days
- Sustained activation of GHRH receptors on pituitary somatotrophs
- Produces continuous GH and IGF-1 elevation rather than pulsatile release
- Less frequent dosing requirement compared to CJC-1295 (no DAC) or sermorelin
Evidence Snapshot
Commonly Discussed Benefits
Safety & Cautions
- Sustained GH elevation may differ from physiological pulsatile release
- May cause water retention and joint stiffness
- Not FDA-approved
- Should be discussed with a healthcare provider
Comparisons
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Citations
- [1] Teichman SL. et al. — Prolonged stimulation of GH and IGF-I by CJC-1295. JCEM. 2006 PubMed
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Related Peptides
CJC-1295
Medium EvidenceA growth hormone releasing hormone analog studied for stimulating growth hormone secretion.
Ipamorelin
Medium EvidenceA selective growth hormone secretagogue studied for targeted GH release with fewer side effects than other GH peptides.
Tesamorelin
High EvidenceA GHRH analog FDA-approved for reducing visceral fat in HIV-associated lipodystrophy.
Sermorelin
Medium EvidenceA GHRH analog previously FDA-approved for growth hormone deficiency diagnosis and treatment.