CJC-1295 With DAC: The 8-Day GHRH Analog, Explained From Its One Human Trial
- Written by
- Daniel Reyes, PhD
- Medically reviewed by
- Dr. Sarah Lindqvist, MD
- Published
- June 20, 2025
- Updated
- June 20, 2025
- Last medical review
- June 20, 2025
- Reviewer scope
- Metabolic health
CJC-1295 with DAC is a GHRH analog engineered to bind serum albumin, stretching its half-life to roughly 6–8 days. Its single published human program showed dose-dependent GH and IGF-1 elevations lasting up to two weeks after one injection. Development stopped, long-term safety was never characterized, and the FDA has flagged it among compounding substances with significant safety risks.
What the phase-I data showed
In healthy adults, single injections produced sustained increases in GH (cumulative) and IGF-1 lasting 6–14 days depending on dose. That paper remains essentially the entire human evidence base — pharmacology, not outcomes.
Why sustained release is the concern, not the selling point
Natural GH secretion is pulsatile; downstream tissues read the pulses. Multi-day flat elevation is a different physiological signal with unknown long-term consequences — the classic worry list includes insulin resistance, fluid retention, and growth signaling in tissue you do not want growing.
The compound usually paired with it has its own file — the ipamorelin guide includes the failed phase-II trial. The pairing itself is graded in our stack evidence review, and the oral alternative in the MK-677 explainer. Compare status across compounds in the peptide comparison table.
DAC vs no-DAC ("Mod GRF 1-29")
Without DAC, the molecule’s half-life drops to minutes, restoring a pulse-like profile — which is why the no-DAC version is often paired with a GHRP like ipamorelin in community protocols. Both versions remain unapproved and safety-flagged.
Frequently asked questions
What is the half-life of CJC-1295 with DAC?
What is the difference between CJC-1295 with and without DAC?
Is CJC-1295 FDA-approved?
Questions to ask a licensed clinician
- Why was development of this compound discontinued?
- How would IGF-1 and glucose be monitored if any GH-axis therapy were appropriate?
References
- Teichman SL, Neale A, Lawrence B, et al. (2006). Prolonged stimulation of GH and IGF-I secretion by CJC-1295 in healthy adults. Journal of Clinical Endocrinology & Metabolism. SourcePhase-I RCT
- US Food and Drug Administration (2023). Certain bulk drug substances for use in compounding that may present significant safety risks. FDA Human Drug Compounding. SourceAgency notice
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