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CJC-1295 (No DAC) vs Sermorelin

Two GHRH(1-29)-based signals. Sermorelin is the native sequence; CJC-1295 No DAC is the same sequence with four amino acid substitutions that resist enzymatic degradation. This page compares what the peer-reviewed literature currently supports on each.

Last reviewed 2026-07-12

  • Peptide structure

    CJC-1295 (No DAC)

    GHRH(1-29) with four amino acid substitutions (D-Ala², Gln⁸, Ala¹⁵, Leu²⁷) that resist DPP-IV and other enzymatic degradation. No albumin-binding modification.

    Sermorelin

    Native GHRH(1-29)NH2 sequence — the shortest fragment of endogenous GHRH that retains full receptor activity. No chemical modifications.

    2 citations in this row

  • Half-life and pulse profile

    CJC-1295 (No DAC)

    ~30 minutes. Produces a physiologic pulsatile GH release, similar in pattern to sermorelin but sustained slightly longer per pulse.

    Sermorelin

    ~10–20 minutes. Produces a shorter, sharper GH pulse — closest of the class to the endogenous pattern.

    1 citation in this row

  • Regulatory status

    CJC-1295 (No DAC)

    Not FDA-approved for any indication. Access via compounding pharmacies or research supply.

    Sermorelin

    Historically FDA-approved as Geref (1990). NDA withdrawn from the U.S. market by the sponsor in 2008 for commercial reasons (not a safety issue). No currently marketed FDA-approved product.

    1 citation in this row

  • Human evidence base

    CJC-1295 (No DAC)

    Human PK/PD data for CJC-1295 primarily cover the DAC form (Teichman JCEM 2006, Ionescu JCEM 2006). The No-DAC form is best supported by preclinical work in GHRH-knockout mice (Alba AJP-Endo 2006). Modern controlled human trial data on No-DAC specifically is limited.

    Sermorelin

    Human data from the Geref era: pediatric GHD trials (Thorner JCEM 1996), adult GH-axis studies (Walker JCEM 1994), and the Prakash 1999 pharmacology review.

    5 citations in this row

  • Reported dosing

    CJC-1295 (No DAC)

    Research contexts commonly report 100–300 µg subcutaneously per pulse, once daily to 3× daily. The 'saturation dose' concept places the plateau around 100 µg per pulse based on preclinical GHRH-receptor kinetics.

    Sermorelin

    Historical Geref pediatric dose: ~30 µg/kg subcutaneously at bedtime. Adult research doses reported in the 200–500 µg/day range in published trials.

    2 citations in this row

  • Position in the GHRH class

    CJC-1295 (No DAC)

    Chemically stabilised research analogue. Its practical advantage vs sermorelin is a somewhat longer half-life without changing the physiologic pulsatile pattern.

    Sermorelin

    The native sequence — the reference peptide for the GHRH(1-29) class. Historical FDA-approved status makes it the class's regulatory benchmark, even without a current active product.

    1 citation in this row

CJC-1295 No DAC and sermorelin share the GHRH(1-29) architecture but sit at different points in their regulatory and evidentiary trajectories. Sermorelin carries a historical FDA legacy and the class's reference sequence. CJC-1295 No DAC is a research-only chemically stabilised variant with a somewhat longer half-life. Neither compound is a substitute for a clinical decision informed by an individual's medical history.

References

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