longevityGHRH analog

CJC-1295

CJC-1295 (without DAC) is the common name for Modified GRF 1-29, a 29-amino-acid analog of endogenous growth hormone releasing hormone (GHRH). It is a truncated and stabilized version of the natural GHRH (44 amino acids), retaining the biologically active N-terminal sequence. The "without DAC" designation is critical, it distinguishes this compound from the DAC (Drug Affinity Complex) version, which has a dramatically different half-life and pharmacodynamic profile.

class
GHRH analog (Modified GRF 1-29)
half-life
~30 min (without DAC)
route
subcutaneous
cadence
1–3× daily (fasted)
storage
refrigerated · 28-day max
typical dose
100 mcg per injection
Dose calculatorlive
U-100
Concentration
1.00mg/mL
Injection vol.
0.100mL
Syringe cap.
100units
Draw to10units
02040608010010 units
vial × bac → conc → vol → unitsverified math · open source
Dosing guide

CJC-1295 Reconstitution & Dosage Protocol

weekly dose · reduces side effects
PhaseWindowWeekly doseDraw (U-100, 2mL BAC)Note
Once dailyPre-bed (most common)0.10 mg10 units· 0.10 mLInject 30–60 min before sleep, fully fasted. Pair with 100–200 mcg ipamorelin.
Twice dailyPre-bed + pre-workout0.10 mg10 units· 0.10 mLSecond injection also requires fasted state, 2+ hours after last meal.
How it works

What is CJC-1295?

CJC-1295 (without DAC) is the common name for Modified GRF 1-29, a 29-amino-acid analog of endogenous growth hormone releasing hormone (GHRH). It is a truncated and stabilized version of the natural GHRH (44 amino acids), retaining the biologically active N-terminal sequence. The "without DAC" designation is critical, it distinguishes this compound from the DAC (Drug Affinity Complex) version, which has a dramatically different half-life and pharmacodynamic profile.

CJC-1295 works by binding to GHRH receptors on somatotroph cells in the anterior pituitary gland, directly stimulating the synthesis and pulsatile release of growth hormone. Unlike exogenous GH injection, which suppresses the hypothalamic-pituitary axis, CJC-1295 amplifies the body's natural GH pulses. This pulsatile pattern more closely mimics endogenous GH secretion and is believed to carry a lower risk of desensitization and side effects than continuous GH elevation.

The without-DAC form has a half-life of approximately 30 minutes, similar to natural GHRH, and clears rapidly, which is essential to preserving the pulsatile mechanism. When combined with a GHRP like ipamorelin, the two peptides produce a synergistic GH pulse that significantly exceeds what either agent achieves alone. CJC-1295 extends the GHRH signal while ipamorelin simultaneously stimulates GH release from the pituitary via the ghrelin receptor, two complementary pathways firing in concert.

A standard 2 mg vial reconstituted with 2 mL of bacteriostatic water gives 1 mg/mL (1,000 mcg/mL). At the typical 100 mcg dose, you draw 0.1 mL, 10 units on a U-100 insulin syringe. Inject subcutaneously in the abdomen 30–60 minutes before sleep in a fully fasted state. Even a small carbohydrate intake raises insulin, which triggers somatostatin release and blocks the GH pulse. Timing and fasting are as important as dosing.

CJC-1295 without DAC is not FDA-approved and is sold exclusively for research purposes. Its use is supported by analogy with well-studied GHRH analogs and extensive mechanistic literature on GHRH receptor pharmacology. The ipamorelin/CJC-1295 combination has a long track record in physician-supervised anti-aging and longevity medicine. All non-physician use is considered research.

Common questions

CJC-1295 Frequently Asked Questions

CJC-1295 without DAC (Modified GRF 1-29) has a half-life of ~30 minutes and produces discrete, pulsatile GH release, mimicking the natural pattern. CJC-1295 with DAC has a half-life of ~7 days due to albumin binding and produces a sustained GH bleed, continuous GH elevation rather than pulses. Most anti-aging protocols prefer the without-DAC form for a more physiological GH pattern.
Sources

Research & References

CJC-1295 combined with GHRP-6, synergistic GH pulse amplificationPubMed · J Clin Endocrinol Metab 2006Modified GRF 1-29 pharmacokinetics and GH secretionPubMed · Endocrinology 2005GHRH receptor agonists in growth hormone deficiencyPubMed · Growth Hormone & IGF Research 2009
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