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CJC-1295 DAC

Long-Acting GHRH with Drug Affinity Complex

Once-weekly GHRH — albumin-binding DAC extends half-life to 6–8 days for sustained GH and IGF-1 elevation.

Tier B — Promising: Some human data + strong preclinical evidence. How our tiers work →
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Research facts

Half-life6–8 days
RouteSubQ
Typical dose1–2 mg/week
FrequencyOnce weekly
SolventBacteriostatic water
pH5.0–7.0
Stability30 days at +4°C

Mechanism of action

CJC-1295 DAC contains the same GHRH(1-29) sequence as the no-DAC version, but incorporates a Drug Affinity Complex — a Lys-maleimide-biotin linker that covalently binds to plasma albumin in the bloodstream. This dramatically extends the active half-life to 6–8 days, producing sustained GH and IGF-1 elevation rather than pulsatile release.

Once-weekly administration maintains elevated mean 24-hour GH and IGF-1 levels, providing a more anabolic background state than pulsatile GHRH. The sustained elevation pattern is less physiological than endogenous pulsatility but potentially more convenient and consistently anabolic. Bryan Johnson documented use of Tirzepatide + CJC-1295 DAC in 2025 as an experimental body composition stack.

Documented effects (research-model)

  • Sustained IGF-1 elevation from once-weekly dosing
  • Body composition improvement via sustained GH axis activation
  • Convenience: weekly rather than daily injection
  • Anti-ageing via prolonged GH/IGF-1 axis support
  • Sleep quality research

Research protocols

ProtocolDoseFrequencyCycleVial
Standard 1 mg once/week Once weekly SubQ 12 weeks 5mg / 2mL BAC water
Advanced 2 mg/week split 2× Twice weekly 12 weeks 5mg / 2mL BAC water

Research context only. Not medical advice. Consult a qualified healthcare professional before any protocol decision.

Synergies

  • Ipamorelin MODERATE
    Sustained GH background (DAC) + triggered pulses (Ipamorelin). Many prefer no-DAC for more physiological pulsatility.
  • Tesamorelin LOW
    Both GHRH analogues — redundant if combined.

Myths & misconceptions

Myth CJC-1295 DAC is better than no-DAC because it lasts longer.
Reality "Better" depends on the goal. DAC provides sustained elevation convenient for once-weekly dosing but is less physiological. No-DAC mimics natural GH pulsatility more closely. No comparative RCT exists in the body composition context.

Evidence gaps

  • No comparative data between DAC and no-DAC versions for specific outcomes in humans.
  • The sustained GH elevation pattern's long-term safety vs. pulsatile remains unknown.
  • Optimal dose in combination protocols not established.

Safety notes

Removed from FDA Category 2 April 2026. The sustained GH elevation warrants careful IGF-1 monitoring. Water retention possible. Less physiological than no-DAC version.

Biomarkers to monitor

IGF-1Fasting GlucoseHbA1cGrowth HormoneInsulin

Primary-source citations

  • PMID 17270313 — Effects of a long-acting GHRH analog on 24-hour growth hormone secretion (J Clin Endocrinol Metab. 2007)

Frequently asked

What is CJC-1295 DAC?

CJC-1295 DAC (Long-Acting GHRH with Drug Affinity Complex) is a research compound classified in our library as Tier B — Some human data + strong preclinical evidence.. Once-weekly GHRH — albumin-binding DAC extends half-life to 6–8 days for sustained GH and IGF-1 elevation.

What is the evidence tier for CJC-1295 DAC?

We classify CJC-1295 DAC as Tier B: Some human data + strong preclinical evidence. See our full peptide evidence tiers explainer for how we assign S/A/B/C/D.

What is the research dose of CJC-1295 DAC?

For CJC-1295 DAC, typical research dose is 1–2 mg/week, route is SubQ, half-life is 6–8 days. Protocols vary by research goal — see the protocols section on this page for standard and advanced dosing schedules. Research use only, not medical advice.

Is CJC-1295 DAC safe?

Removed from FDA Category 2 April 2026. The sustained GH elevation warrants careful IGF-1 monitoring. Research context only — no compound on this site is approved for human therapeutic use unless explicitly noted.

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