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CJC-1295 (No-DAC)Growth Hormone

Short-acting GHRH analog (Mod GRF 1-29) studied for growth-hormone release; often paired with Ipamorelin.

Rating1/5SpeculativeHuman dataSafety
Compare prices — from $42.96
StatusResearch only
FDA-approvedNO
PrescriptionNO
From$42.96

Overview

CJC-1295 (No-DAC) — better known as Modified GRF 1-29 (mod GRF 1-29) — is the short-acting form of the CJC-1295 GHRH analog. It is the tetrasubstituted [D-Ala2, Gln8, Ala15, Leu27] version of growth-hormone-releasing hormone's first 29 amino acids, without the albumin-binding Drug Affinity Complex (DAC) that defines the long-acting CJC-1295 DAC version. The four substitutions protect it from enzymatic breakdown, giving a half-life of ~30 minutes versus under 10 minutes for native GRF(1-29) — but it is still short-acting, producing only a brief GH pulse. It is research-use-only and not FDA-approved.

How it works

Mod GRF 1-29 binds the GHRH receptor on pituitary somatotrophs and stimulates a pulsatile release of the body's own growth hormone, which raises hepatic IGF-1. Because it lacks the DAC albumin-binding tail, the peptide is cleared within roughly 30 minutes, so each dose produces a single short GH pulse that mimics natural GHRH pulsatility. This is why it is typically dosed several times per day and usually combined with a ghrelin-receptor agonist (a GHRP such as ipamorelin) for a synergistic pulse — in contrast to the steady, multi-day GH/IGF-1 elevation of the DAC form.

Evidence

There are no dedicated controlled human trials of the no-DAC form. The early-phase human pharmacokinetic studies usually attributed to "CJC-1295" actually used the DAC version; they established the tetrasubstituted GRF(1-29) backbone but not this short-acting peptide's clinical effects. Evidence for mod GRF 1-29 specifically is limited to its known GHRH-agonist pharmacology and anecdotal use; no trial demonstrates a body-composition, performance, or anti-aging outcome.

Safety

Human safety data are sparse and short-term. Commonly reported effects are injection-site reactions, transient flushing/head-rush, and water retention or tingling; as a GH secretagogue it can raise GH/IGF-1 and may affect glucose metabolism with frequent use. There are no long-term or large-population safety data, and research-grade material is of unverified purity. It is prohibited in sport (WADA S2) and not FDA-approved. Research use only — nothing here is therapeutic or dosing guidance.

Reported side effects

Reported in published literature and user reports. Not a complete list, and not medical advice.

  • Injection-site reactions (redness, itching, pain)
  • Flushing, head-rush, headache
  • Transient water retention or tingling
  • Possible IGF-1 / glucose effects with frequent use

If severe or unexpected symptoms occur, contact a qualified medical professional. PEPTIDES·INDEX does not provide medical advice.

Cautions discuss with a clinician

Use caution or avoid if
  • No human contraindication data exist for the no-DAC form; the following are grounded theoretical cautions, not established medical contraindications.
  • Active or prior cancer is a theoretical concern because raising the GH/IGF-1 axis activates mitogenic signaling.
  • Diabetes or impaired glucose tolerance, since GH secretagogues can affect glucose metabolism.
Interactions
  • CorticosteroidsMay blunt the GH response (class effect of GHRH/GHRP agents)
  • Insulin or other glucose-lowering agentsGH-axis stimulation can alter glucose handling; net effect in humans is uncharacterized (research use only)

Timeline commonly reported

  1. Per dose (acute)

    Triggers a short GH pulse within ~15–30 min that subsides within a couple of hours — the short half-life is why it is dosed multiple times per day, usually paired with a GHRP.

  2. Weeks 4–12

    Any body-composition or recovery changes are anecdotal; there are no dedicated controlled human trials of the no-DAC form.

FAQ

What is the difference between CJC-1295 (No-DAC) and CJC-1295 DAC?

No-DAC CJC-1295 is Modified GRF 1-29, a short-acting GHRH analog with a half-life of about 30 minutes that produces a single brief GH pulse and is dosed several times a day. CJC-1295 DAC adds an albumin-binding Drug Affinity Complex that extends the half-life to roughly 6-8 days for sustained GH/IGF-1 elevation.

Is CJC-1295 (No-DAC) FDA-approved?

No. It has no FDA approval for any indication and is sold strictly as a research-use-only chemical. There are no dedicated controlled human trials of the no-DAC form.

Is CJC-1295 banned in sport?

Yes. As a growth-hormone secretagogue / GHRH analog it is prohibited at all times under WADA category S2.

How is CJC-1295 (No-DAC) used in reported protocols?

Because the no-DAC form clears within about 30 minutes, anecdotal protocols dose it subcutaneously one to three times a day rather than weekly, often timed around bedtime or training. These are commonly reported figures, not validated by any controlled human trial, and the compound is research-use-only.

Why is CJC-1295 (No-DAC) usually combined with a GHRP like ipamorelin?

It acts on the GHRH receptor, while a GHRP such as ipamorelin acts on the separate ghrelin/GHS-R1a receptor. Stacking the two is reported to produce a larger, complementary GH pulse than either alone, which is why mod GRF 1-29 is typically paired with a GHRP in research settings.

How does the GH pulse from CJC-1295 (No-DAC) compare to the DAC form?

The no-DAC form mimics natural GHRH pulsatility, generating a single short GH pulse that subsides within a couple of hours. The DAC form instead binds albumin to give a sustained, multi-day elevation of GH and IGF-1, which is a fundamentally different exposure profile.

Related guides

Sources

Starting references for the library summary. These are not dosing instructions or medical advice.

For research-use educational context only. Not medical advice and not a recommendation to use any compound. Consult a qualified healthcare professional before any health decision.