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Growth Hormone Axis

CJC-1295 (with DAC)

The long-acting version of CJC-1295. One injection lasts about a week because it grabs onto a blood protein (albumin). Instead of a single sharp pulse, it raises your GH/IGF-1 baseline for days; convenient, but less “natural” than the No-DAC pulse.

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Research & reference information

This profile compiles research and community-sourced reference information for educational purposes. Information may evolve as research and community knowledge develop. It is not individualized medical advice.

Overview

The long-acting version of CJC-1295.

One injection lasts about a week because it grabs onto a blood protein (albumin).

Instead of a single sharp pulse, it raises your GH/IGF-1 baseline for days; convenient, but less “natural” than the No-DAC pulse.

What It Does

CJC-1295 DAC is a GHRH analog with a Drug Affinity Complex that binds reversibly to albumin, extending half-life from minutes (No-DAC) to ~6– 8 days.

This produces a sustained elevation of GH and IGF-1 (a continuous “bleed”) rather than the pulsatile release of the No-DAC version.

Convenient weekly dosing; the trade-off is loss of natural GH pulsatility.

Reconstitution

Vial SizeBAC Water / SolventConcentration
2 mg+ 1 mL2 mg/mL
Interactive tool

Reconstitution Calculator

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Protocol

PhaseFrequencyAmountNotes
Weeks 1–2Once weekly1 mgStart at the low end; the long half-life means levels build over the first 1–2 weeks.
Weeks 3–12Once weekly (or split 2×/wk)2 mg/weekStandard. Splitting into 2 doses/week smooths levels and side effects.
Off4 weeks–Let IGF-1 normalize before re-cycling.
Cycle & Timing

8–12 weeks on / 4 weeks off.

Timing

Any time of day (long half-life makes timing far less critical than No-DAC). Pair with a GHRP if a stronger pulse is wanted. DAC vs No-DAC: DAC = convenience + sustained levels; No-DAC = physiological pulses. Many prefer No-DAC for a more natural profile.

Population Considerations

Women make ~3× the GH of men yet have similar IGF-1, they’re less responsive, so often need a higher dose to move IGF-1. Oral estrogen blunts IGF-1 further (read it as running low); a skin patch/gel is more predictable. Men: Men convert GH to IGF-1 more efficiently and more often overshoot the age ceiling (a higher malignancy signal), aim mid-normal for age, don’t chase the Women make ~3× the GH of men yet have similar IGF-1, they’re less responsive, so often need a higher dose to move IGF-1. Oral estrogen blunts IGF-1 further (read it as running low); a skin patch/gel is more predictable. Men: Men convert GH to IGF-1 more efficiently and more often overshoot the age ceiling (a higher malignancy signal), aim mid-normal for age, don’t chase the top.

Handling & Stacking

Injection site
SubQ, abdomen. Rotate.
Storage
  • Freeze-dried: -4°F.
  • Reconstituted: 36–46°F.
  • Best used within ~2–4 weeks, kept cold (structure-based estimate, no published data); that is close to the 28- day sterility limit, so use whichever comes first.
  • Avoid freeze-thaw.
Side effects
Water retention, tingling/numbness, head rush/flushing after dosing, joint aches; can be more pronounced than No-DAC due to sustained levels.
What to expect
Sleep, recovery, and body-composition gains over 8–12 wks with weekly dosing; sustained IGF-1; monitor it. Supply math 2mg → 12 vials (12-wk @ 2 mg/week)
Pairs well with
Ipamorelin / GHRP-2 (GHRP for added pulse); Wolverine Blend (recovery). Note: pairs less “pulsatile” than No-DAC + GHRP
Avoid
Active malignancy. Severe insulin resistance. Stacking with No-DAC CJC (redundant). Sustained high-dose use without IGF-1 monitoring
Approved drug
Somatropin (HGH) is approved for growth-hormone deficiency and tesamorelin (Egrifta) for HIV lipodystrophy. Secretagogues like this one are off-label.

Safety & Patient Education

Contraindications
Active malignancy of any kind (GH/IGF-1 can promote tumor growth) Severe diabetic retinopathy Acute critical illness (per somatropin label) Pregnancy and lactation
Warnings
Sustained (non-pulsatile) GH/IGF-1 elevation, further from physiology than No-DAC; monitor IGF-1 closely Insulin resistance with sustained use Fluid retention, carpal tunnel, joint pain; often more than No-DAC Long half-life means side effects persist for days after a dose IGF-1 elevation: theoretical malignancy promotion beyond physiological ranges
Drug interactions
Glucocorticoids: blunt GH response Insulin / antidiabetics: GH worsens insulin resistance, monitor glucose Levothyroxine: GH lowers free T4, recheck TSH/fT4 quarterly Oral estrogens: blunt GH-stimulated IGF-1
Labs
  • IGF-1 (baseline + Week 4 + Week 8 + end), sustained levels make monitoring more important Fasting glucose / HbA1c (baseline + end) Age-appropriate cancer screening before starting Out of range?
  • IGF-1 above your age range = too much growth signal (feeds hidden cancer, enlarges organs) → drop the dose; rising glucose/HbA1c = sugar creeping up.
Stop criteria
IGF-1 above upper limit of normal for age Fasting glucose rises >20 mg/dL above baseline New persistent joint pain or carpal tunnel symptoms New skin changes or enlarging moles; vision changes
Patient education
One weekly dose keeps GH/IGF-1 elevated for days, convenient but less natural than pulsatile No-DAC Monitor IGF-1 more closely than with short-acting GH peptides Not for use during active malignancy or pregnancy; report new lumps or vision changes
References
researchdosing · peptidedosages · PubMed · thepeptidereport · Span 2000 · Weissberger 1991