Growth Hormone-Releasing Hormone (GHRH) Analog
    ·Educational Resource · Research-Use Only

    CJC-1295

    The modified GHRH analog — available with or without DAC, the foundation of the most-studied research GH stack.

    Class
    Modified GHRH 1-29 analog
    Variants
    No-DAC (~30 min) · With-DAC (6–8 days)
    Stack Partner
    Ipamorelin (most common)
    Standard Dose (no-DAC)
    100 mcg, 1–3×/day
    On This Page

    What Is CJC-1295?

    CJC-1295 is a synthetic 30-amino-acid analog of growth-hormone-releasing hormone (GHRH 1-29), with four amino-acid substitutions that protect it from the rapid enzymatic breakdown that limits the half-life of native GHRH and sermorelin.

    It exists in two distinct forms. CJC-1295 'no-DAC' (also called Modified GRF 1-29) is the bare modified peptide with a half-life of roughly 30 minutes — long enough to produce a clean GH pulse, short enough to mimic physiological release. CJC-1295 'with DAC' has an additional Drug Affinity Complex that bonds to circulating albumin, extending the half-life to roughly 6–8 days and producing a continuous (rather than pulsatile) elevation in baseline GH.

    Choice of variant is a major design decision in research protocols. No-DAC is preferred when pulsatility matters (sleep, muscle/fat outcomes, replicating natural rhythm). With-DAC is studied when sustained IGF-1 elevation is the goal (some body-composition and tissue-repair contexts).

    History & Discovery

    CJC-1295 was developed at ConjuChem, a Montreal-based biotech, in the early 2000s as part of a broader platform exploring drug-affinity-complex (DAC) chemistry for half-life extension. The starting molecule was GHRH 1-29 — the biologically active fragment of native GHRH that had previously been developed as sermorelin.

    The medicinal-chemistry team made four amino-acid substitutions (D-Ala²⁸, Gln³⁸, Ala¹⁵, Leu²⁷) to protect the molecule from DPP-4 and trypsin cleavage. This 'modified GRF 1-29' became what is now sold as CJC-1295 without DAC.

    The 'with DAC' variant adds a maleimidopropionic acid (MPA) linker that covalently bonds to a free cysteine on circulating serum albumin, extending the half-life from minutes to days — turning a pulsatile GHRH analog into a near-continuous one. This was the original commercial product ConjuChem advanced through phase 1 and phase 2 trials.

    ConjuChem discontinued the CJC-1295-with-DAC clinical program in the late 2000s — the molecule produced sustained GH/IGF-1 elevation but raised questions about whether continuous receptor stimulation was physiologically appropriate. The compound entered the research-peptide ecosystem in both forms and is now overwhelmingly used as the no-DAC variant in stacked GH research.

    Mechanism of Action

    Like all GHRH analogs, CJC-1295 binds the GHRH receptor on somatotroph cells of the anterior pituitary, stimulating endogenous growth hormone release. The body's negative feedback through somatostatin remains intact, distinguishing GHRH-driven GH release from exogenous rhGH administration.

    The four amino-acid substitutions in CJC-1295 (D-Ala at position 2, Gln at 8, Ala at 15, Leu at 27) protect the molecule from dipeptidyl peptidase-4 (DPP-4) and other proteases that would otherwise degrade native GHRH within minutes.

    The DAC variant adds a maleimidopropionic acid (MPA) group that covalently bonds to a cysteine residue on serum albumin, creating an albumin-CJC-1295 complex that circulates for days — the body's GHRH receptor sees a continuous low-level stimulus rather than a pulse.

    Pharmacokinetics

    Molecular weight (no-DAC)3,367 Da
    Molecular weight (with-DAC)~3,648 Da (plus albumin conjugate ~70 kDa)
    Receptor targetGHRH receptor (GHRHR) on pituitary somatotrophs
    Time to peak GH (no-DAC)~15–30 minutes after subcutaneous injection
    Half-life (no-DAC)~30 minutes (functional GH-stimulation window 1–2 hours)
    Half-life (with-DAC)Approximately 6–8 days
    Steady-state IGF-1 rise (with-DAC)Plateau by week 2 of weekly dosing
    Feedback preservationYes — somatostatin negative feedback intact

    Research Use Cases

    Synergistic GH Pulse with GHRP

    The most common research configuration: CJC-1295 (no-DAC) stacked with ipamorelin or another GHRP for amplified pulsatile GH release.

    Sustained IGF-1 Elevation

    CJC-1295 with DAC has been studied for its ability to maintain elevated IGF-1 over multiple days from a single weekly injection.

    Body Composition Research

    Investigated for lean-mass preservation and adipose reduction, particularly in aging populations with declining endogenous GH secretion.

    Recovery and Tissue Repair

    Studied in contexts where elevated GH/IGF-1 is hypothesized to support connective-tissue and post-exercise recovery.

    Sleep Architecture

    No-DAC CJC-1295 dosed in the evening has been studied for its effect on slow-wave sleep restoration in adult research subjects.

    GH-Axis Restoration in Somatopause

    Used as a research tool to investigate physiological-pattern GH restoration without the supraphysiologic spikes of exogenous rhGH.

    Research Dosing Reference

    Research-only reference. The protocols below are aggregated from the published research literature and not a recommendation for personal use. No peptide in this category is FDA-approved for self-administration outside of cleared indications.

    CJC-1295 no-DAC + Ipamorelin (canonical research stack)

    The dominant research configuration. Often shorthanded as 'CJC/Ipa 100/100'.

    Dose
    100 mcg CJC-1295 + 100 mcg ipamorelin per administration
    Frequency
    1–3 times daily; pre-bed dose is the most important
    Route
    Subcutaneous (drawn together in a single insulin syringe)

    CJC-1295 no-DAC — solo research dosing

    Less common than the stacked configuration but used in research isolating GHRH-arm effects.

    Dose
    100–200 mcg per administration
    Frequency
    1–2 times daily
    Route
    Subcutaneous

    CJC-1295 with DAC — research dosing

    The with-DAC profile is sustained, not pulsatile. Used in research targeting steady IGF-1 elevation rather than physiological pulse restoration.

    Dose
    1–2 mg per administration
    Frequency
    Once weekly (typically Sunday evening)
    Route
    Subcutaneous

    Body recomposition saturation schedule

    Aggressive pulse-frequency schedule used in body-recomposition research contexts.

    Dose
    100 mcg CJC-1295 + 200–300 mcg ipamorelin
    Frequency
    3 times daily — AM fasted, post-workout, pre-bed
    Route
    Subcutaneous

    Stacking & Combinations

    CJC-1295 no-DAC + Ipamorelin

    The defining stack of modern GH-axis research. CJC-1295 primes somatotrophs to release GH via GHRH-receptor activation; ipamorelin amplifies the magnitude of release through the parallel ghrelin-receptor pathway. Combined GH pulse is roughly 2–4× larger than either compound alone.

    CJC-1295 no-DAC + GHRP-2 or hexarelin

    Mechanistically equivalent to the ipamorelin pairing — any GHRP partner will produce the synergistic pulse amplification. Less common in modern research because GHRP-2 elevates cortisol/prolactin and hexarelin can desensitize the receptor with chronic use.

    CJC-1295 with DAC (standalone)

    The with-DAC variant is typically used solo because its sustained-release profile already provides continuous GHRH stimulation — adding a GHRP often produces excessive IGF-1 elevation. Research is sparse compared to the no-DAC stack.

    CJC-1295 + Tesamorelin (combined GHRH approach)

    Rarely used. Both compounds act on the same receptor — combining them does not increase efficacy beyond the maximal GHRH pulse and adds cost and side-effect burden. Mentioned only to clarify it is not a recommended research configuration.

    Side Effect Profile

    Common / Mild-to-Moderate

    • •Mild flushing or warmth in the first 5–10 minutes after injection
    • •Transient lightheadedness shortly after injection
    • •Injection-site reactions (redness, itching, mild swelling)
    • •Mild water retention in the first 1–2 weeks
    • •Vivid dreams / altered sleep architecture (expected GH-axis effect)
    • •Numbness or tingling in extremities (dose-related, GH-axis carpal-tunnel-like)

    Serious / Less Common

    • •Glycemic dysregulation in predisposed subjects, more pronounced with with-DAC due to sustained IGF-1 elevation
    • •Hypersensitivity reactions (rare)
    • •Theoretical concern: contraindicated in active malignancy (GH/IGF-1 elevation)
    • •With-DAC specifically: edema and joint pain are more common at supratherapeutic doses

    Side effect profile is dose- and variant-dependent. The no-DAC variant in stacked research dosing has a favorable acute profile. With-DAC is associated with more pronounced metabolic effects due to its continuous-stimulation profile. Standard research practice includes periodic IGF-1 and fasting glucose monitoring.

    Storage & Reconstitution

    • Lyophilized vials are stored refrigerated at 2–8°C. CJC-1295 is reasonably stable at room temperature for short shipping intervals.
    • Reconstitute with bacteriostatic water for injection. For a 5 mg vial, 2 mL is the most common volume — yielding 2.5 mg/mL.
    • Inject the BAC water against the vial wall slowly. Swirl gently — never shake — until fully dissolved.
    • Once reconstituted, store refrigerated. The no-DAC variant is stable for approximately 30 days for research use; the with-DAC variant has a similar shelf life.
    • CJC-1295 and ipamorelin are commonly drawn into the same syringe and injected together. Both are stable at neutral pH in BAC water.
    • Use a 31G insulin syringe. For a 2.5 mg/mL concentration, 100 mcg = 0.04 mL = 4 units on a 100-unit insulin syringe.
    • Inject subcutaneously, rotating between abdomen and posterior arms. Pre-bed timing aligns with the natural overnight GH pulse.

    Key Studies & Trial Data

    CJC-1295 with DAC: prolonged GH/IGF-1 elevation in healthy adults

    2006

    ConjuChem's phase 1 work on CJC-1295 with DAC. Single subcutaneous doses produced detectable GH and IGF-1 elevation lasting 6–11 days — the foundational pharmacokinetic dataset for the with-DAC variant.

    Teichman SL, et al. J Clin Endocrinol Metab. 2006;91(3):799–805.

    Long-term safety and PK of CJC-1295 with DAC

    2007

    Multi-dose phase 1 safety and pharmacokinetic study. Weekly subcutaneous CJC-1295 with DAC produced sustained IGF-1 elevation with mild edema and arthralgia at higher doses — establishing the safety envelope used in subsequent research.

    Ionescu M, Frohman LA. J Clin Endocrinol Metab. 2006;91(12):4792–4797.

    GHRH + GHRP synergy mechanism (foundational)

    1995

    Foundational study establishing that combined GHRH and GHRP administration produces a GH pulse 2–4× larger than either alone — the mechanistic basis for the modern CJC-1295 + ipamorelin stack.

    Bowers CY. J Clin Endocrinol Metab. 1996;81(10):3501–3507 (and subsequent work).

    Comparisons & Deep Dives

    In-depth articles on Peptide Basics that compare CJC-1295 to related compounds and expand on its mechanism and use.

    Frequently Asked Questions

    Where to Source Research-Grade CJC-1295

    Trusted Research Source

    Base Peptide

    Research-grade CJC-1295 (no-DAC and with-DAC variants available) with batch-specific Certificate of Analysis. The standard GHRH partner for the dominant ipamorelin research stack.

    View CJC-1295 (no-DAC) 5mg on BasePeptide.com

    Other reputable suppliers known for batch-specific Certificates of Analysis:

    Want a deeper, ongoing reference? Peptide Basics maintains a comprehensive resource on CJC-1295 alongside calculators, reconstitution guides, and a database of 60+ research peptides.

    Read more on Peptide Basics
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