CJC-1295 (with DAC) vs CJC-1295 (no DAC): Research Comparison

Built from the CJC-1295 (with DAC), CJC-1295 (no DAC) research profiles · Profiles last updated October 1, 2026 · Reviewed by The Peptide Dispatch Editorial Team

TL;DR

This page compares CJC-1295 (with DAC) and CJC-1295 (no DAC) using only their research-profile data. CJC-1295 (with DAC) (research stage: Phase 1 / early human; half-life: 6-8 days). It is a long-acting version of the hormone that tells the pituitary to release growth hormone, so its effect lasts for days. CJC-1295 (no DAC) (research stage: Preclinical (animal); half-life: Not established in published research). It is expected to prompt the pituitary gland to release growth hormone, based on similar compounds; it has not been studied directly. Educational summary, not medical advice.

Where each point comes from: Clinicalhuman trials and FDA labels   Lab / animalrodent, cell and ex vivo studies   Community-reporteduser experience and commonly used protocols, not from clinical studies

Educational summary. Everything below is taken from each compound's research profile and describes what was reported in the cited studies — not a promise of results, a dose recommendation, or an endorsement for human use. Not medical advice. Full disclaimer.

Side-by-side comparison

CJC-1295 (with DAC)CJC-1295 (no DAC)
CategoryGrowth HormoneGrowth Hormone
Research statusPhase 1 / early humanPreclinical (animal)
Regulatory note (as of Sept 2026)Not FDA-approved. Not among the peptides named in the 2026 PCAC actions.
Regulatory tracker →
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Regulatory tracker →
Half-life6-8 daysNo published PK data found
Administration routeSubcutaneous injectionSubcutaneous injection
Dosing used in published research (not a recommendation)Healthy adults aged 21-61: single s.c. ascending doses, then 2-3 weekly or biweekly s.c. doses. Best tolerated at 30 or 60 µg/kg (Teichman 2006). That is about 2-4 mg per dose for a 70 kg adult, given once, weekly or every 2 weeks, over 28-49 days.No published studies of Mod GRF(1-29)/CJC-1295 no DAC found. CJC-1295 with DAC: 30 or 60 µg/kg s.c. single/weekly doses in healthy adults. Sermorelin: 1 µg/kg i.v. as a diagnostic GH stimulation test in children.
Community-reported protocol (not from clinical studies)Community-reported1–2 mg per week, subcutaneous injectionCommunity-reported100–200 mcg, subcutaneous injection
How it works (as summarized from the cited research)In plain terms: It is a long-acting version of the hormone that tells the pituitary to release growth hormone, so its effect lasts for days. GHRH analogue with a drug affinity complex (DAC) modification designed to bind albumin and prolong its action. In two placebo-controlled trials in healthy adults, single and repeated subcutaneous doses produced prolonged increases in GH and IGF-I (Teichman 2006).In plain terms: It is expected to prompt the pituitary gland to release growth hormone, based on similar compounds; it has not been studied directly. Proposed mechanism, inferred from related GHRH analogues (no published studies of this compound were found): a GHRH-receptor agonist expected to stimulate pituitary GH release. The related GHRH analogue sermorelin (GRF 1-29) stimulates GH secretion from the anterior pituitary (Prakash 1999).
Effects reported in research (study subjects as stated)
  • ClinicalRaised GH 2-10-fold for ≥6 days and IGF-I 1.5-3-fold for 9-11 days in healthy adults (Teichman 2006)
  • Lab / animalIn animal studies: enhanced GH release
  • Body composition, recovery, sleep and anti-aging effects are hypothesized based on GHRH pharmacology; no published studies of this compound
Potential side effects
  • ClinicalNo serious adverse reactions in the Teichman 2006 trials; tolerability was best at 30-60 µg/kg
  • Long-term human safety data are lacking
  • No published human safety data for the no-DAC form
  • ClinicalFor CJC-1295 with DAC: injection-site reactions and no serious adverse events in 28-49 day trials (PMID 16352683)
Profile descriptionCJC-1295 with Drug Affinity Complex that extends half-life dramatically, providing sustained GH elevation over days rather than hours.Modified Growth Hormone Releasing Factor (1-29), proposed to provide more stable GH release when combined with GHRPs (no primary study found). Also known as Mod GRF 1-29.
References cited on the profile12

Key differences in the published research

  • Research status: CJC-1295 (with DAC) — Phase 1 / early human; CJC-1295 (no DAC) — Preclinical (animal).
  • Category: the same on every profile (Growth Hormone).
  • Reported half-life: CJC-1295 (with DAC) — 6-8 days; CJC-1295 (no DAC) — No published PK data found.
  • Administration route in the literature: the same on every profile (Subcutaneous injection).
  • Evidence cited: CJC-1295 (with DAC)’s profile lists 1 reference; CJC-1295 (no DAC)’s profile lists 2 references.

Regulatory status

  • CJC-1295 (with DAC): Not FDA-approved. Not among the peptides named in the 2026 PCAC actions. Details →
  • CJC-1295 (no DAC): No regulatory note on its profile. Details →

For the sourced, dated status of every peptide in FDA's 2026 compounding actions, see the FDA peptide regulatory tracker.

Frequently Asked Questions

Which has more human data?
Going by the research status on each profile (CJC-1295 (with DAC): Phase 1 / early human; CJC-1295 (no DAC): Preclinical (animal)), CJC-1295 (with DAC) is furthest along in human testing. Research status describes the stage of the published evidence, not whether a compound works or is safe.
What are the half-lives?
CJC-1295 (with DAC): 6-8 days. CJC-1295 (no DAC): No published PK data found. Figures are as reported in the cited studies, with the species where stated.
Are they FDA-approved?
CJC-1295 (with DAC): research status “Phase 1 / early human”. Not FDA-approved. Not among the peptides named in the 2026 PCAC actions. CJC-1295 (no DAC): research status “Preclinical (animal)”. See the FDA peptide regulatory tracker for sourced compounding status.
How are they administered in the research?
CJC-1295 (with DAC): Subcutaneous injection. CJC-1295 (no DAC): Subcutaneous injection. This describes the published studies and is not a recommendation for human use.
How do their proposed mechanisms differ?
CJC-1295 (with DAC): In plain terms: It is a long-acting version of the hormone that tells the pituitary to release growth hormone, so its effect lasts for days. GHRH analogue with a drug affinity complex (DAC) modification designed to bind albumin and prolong its action. In two placebo-controlled trials in healthy adults, single and repeated subcutaneous doses produced prolonged increases in GH and IGF-I (Teichman 2006). CJC-1295 (no DAC): In plain terms: It is expected to prompt the pituitary gland to release growth hormone, based on similar compounds; it has not been studied directly. Proposed mechanism, inferred from related GHRH analogues (no published studies of this compound were found): a GHRH-receptor agonist expected to stimulate pituitary GH release. The related GHRH analogue sermorelin (GRF 1-29) stimulates GH secretion from the anterior pituitary (Prakash 1999). These are mechanisms proposed in the cited research, at the research stage listed for each compound.

References

CJC-1295 (with DAC)

  1. Prolonged stimulation of growth hormone (GH) and insulin-like growth factor I secretion by CJC-1295, a long-acting analog of GH-releasing hormone, in healthy adults
    Teichman SL, Neale A, Lawrence B, Gagnon C, Castaigne JP, Frohman LA. The Journal of clinical endocrinology and metabolism. 2006. PMID: 16352683.
    Study type: Two randomized placebo-controlled ascending-dose trials, healthy adults.
    DOI: 10.1210/jc.2005-1536 · PubMed

CJC-1295 (no DAC)

  1. Sermorelin: a review of its use in the diagnosis and treatment of children with idiopathic growth hormone deficiency
    Prakash A, Goa KL. BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy. 1999. PMID: 18031173.
    Study type: Drug review (GRF 1-29 analog).
    DOI: 10.2165/00063030-199912020-00007 · PubMed

Read the full profiles

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Educational content — not medical advice. Effects described are drawn from cited research in study subjects.

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