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Phase IIVendors pendingFacts verified · 2026-05-25

CJC-1295 (with DAC)

Also known as cjc-1295 dac, dac-grf(1–29) · Wikipedia

CJC-1295 with DAC (DAC-GRF(1-29)) is a tetrasubstituted analog of human GHRH(1-29) bearing a Drug Affinity Complex - a maleimidopropionyl-lysine at the C-terminus that forms a covalent bond with cysteine-34 of circulating serum albumin, converting the molecule into a long-acting depot (https://pubmed.ncbi.nlm.nih.gov/15817669/). Originally developed by ConjuChem and advanced to Phase II, CJC-1295 produces sustained elevations of GH and IGF-1 lasting days to weeks per injection (https://pubmed.ncbi.nlm.nih.gov/19386527/). Clinical development was discontinued and the molecule is sold only as a research chemical. It is WADA-prohibited and not FDA-approved for any indication. Also known as: CJC-1295 DAC; DAC-GRF(1-29).

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Mechanism of action

CJC-1295 with DAC is the same tetrasubstituted (D-Ala2, Gln8, Ala15, Leu27) GHRH(1-29) analog as mod-GRF, modified at the C-terminus with a maleimidopropionic-acid lysine (Drug Affinity Complex) that covalently binds Cys-34 of serum albumin via Michael addition (https://pubmed.ncbi.

CJC-1295 with DAC is the same tetrasubstituted (D-Ala2, Gln8, Ala15, Leu27) GHRH(1-29) analog as mod-GRF, modified at the C-terminus with a maleimidopropionic-acid lysine (Drug Affinity Complex) that covalently binds Cys-34 of serum albumin via Michael addition (https://pubmed.ncbi.nlm.nih.gov/15817669/). This converts the peptide into a slow-release depot, extending plasma half-life from minutes to roughly 6-8 days. The intact albumin-conjugated molecule still engages the pituitary GHRH receptor and stimulates GH secretion, but - unlike endogenous pulsatile GHRH - produces a sustained 'bleed' of GH and downstream IGF-1 rather than discrete physiologic pulses, blunting normal pulsatile rhythm (https://pmc.ncbi.nlm.nih.gov/articles/PMC2787983/). In ConjuChem Phase I trials, single doses produced 2- to 10-fold mean GH increases for up to 6 days and IGF-1 elevation persisting 9-11 days.

Pharmacokinetic properties

Half-life

~6-8 days (due to albumin binding)

Routes

subcutaneous

Bioavailability

Long-acting depot effect via covalent albumin conjugation; once- or twice-weekly dosing typical.

Amino-acid sequence

Tyr-D-Ala-Asp-Ala-Ile-Phe-Thr-Gln-Ser-Tyr-Arg-Lys-Val-Leu-Ala-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Leu-Ser-Arg (C-terminal Lys modified with maleimidopropionyl (DAC))

Use & research dosing

Original ConjuChem Phase I/II trials in healthy adults used single SC doses of 60, 90, 125, and 250 mcg/kg, producing dose-dependent GH peaks and sustained IGF-1 elevation for 6-11 days post-injection (https://pmc.ncbi.nlm.nih.gov/articles/PMC2787983/). Self-experimentation protocols typically report fixed doses of 1-2 mg subcutaneously per week, often split into 500 mcg to 1 mg twice weekly. There is no FDA-approved dose; clinical development was halted at Phase II and the molecule is sold only as a research chemical.

Research-use framing only. SavePeptides sells nothing for human consumption. Doses above reflect reported research / self-experimentation ranges, not clinical recommendations.

Editorial perspective

The defining feature of CJC-1295 with DAC is its sustained non-pulsatile GH elevation, which differs fundamentally from endogenous pulsatile GHRH and from short-acting GHRH analogs like mod-GRF/sermorelin. Many protocol authors prefer the no-DAC version specifically to preserve physiologic pulsatility. Clinical development was discontinued after Phase II for reasons not fully detailed in peer-reviewed literature; this is the principal reason the molecule remains a research chemical despite well-characterized pharmacology in the published Phase I/II reports.

— SavePeptides editorial desk · last updated 2026-05-25

Cautions & contraindications

Before researching this compound, note:

  • Not FDA-approved for any indication; ConjuChem clinical development halted at Phase II
  • Sustained (non-pulsatile) GH and IGF-1 elevation differs from physiologic pulsatile release and may carry distinct long-term risk profile (cardiomyopathy, insulin resistance, neoplasia)
  • Avoid in active or suspected malignancy due to mitogenic effects of IGF-1
  • Avoid in pregnancy, breastfeeding, and active proliferative diabetic retinopathy
  • Injection-site reactions, facial flushing, headache, and fluid retention reported in Phase I trials (https://pmc.ncbi.nlm.nih.gov/articles/PMC2787983/)
  • May worsen insulin sensitivity and impair glucose tolerance via sustained GH excess
  • Reports of a death in a Phase II ConjuChem program (causality unclear and not formally adjudicated in the peer-reviewed literature) - a cautionary signal that contributed to discontinuation
  • WADA-prohibited (S2: peptide hormones, growth factors, related substances)
  • Vendor purity and dose accuracy are unverified - research-chemical market only

Facts verified

2026-05-25

Confidence

medium

What this means

  • clinical development halted at Phase II; reports of death in trial not formally adjudicated in peer-reviewed literature

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