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CJC-1295 (no DAC / Mod GRF 1-29)

A short-acting GHRH analog — and a clear explanation of DAC vs. no-DAC.

Published Aug 19, 2026 · Updated Sep 19, 2026

CJC-1295 5mg (no DAC)

CJC-1295 without DAC is a synthetic 29-amino-acid analog of growth-hormone-releasing hormone. It is studied as a tool for driving the body’s own growth-hormone production — rather than supplying growth hormone directly — and its defining feature is a deliberately short duration of action.

What you’re reading about — with DAC vs. without

This is the single most confused point about this compound, so here it is plainly:

  • CJC-1295 without DAC — also called Modified GRF (1-29) or Mod GRF 1-29. Short half-life, producing a brief pulse of GH release. This is the compound profiled here.
  • CJC-1295 with DAC — carries a Drug Affinity Complex that binds albumin and extends its half-life to days, producing a sustained elevation instead of a pulse. A different research tool with a different profile.

The distinction matters: the two behave differently enough that findings for one should not be assumed to transfer to the other.

Mechanism under investigation

As a GHRH analog, it binds the GHRH receptor on the pituitary and stimulates release of endogenous growth hormone. Because the no-DAC version clears quickly, the resulting release is pulsatile — closer to the body’s natural rhythm, in which GH is secreted in bursts rather than held at a constant level. That physiological patterning is precisely why researchers reach for it.

Research applications

  • GHRH-receptor signaling and pituitary function.
  • Pulsatile versus sustained GH release — a direct comparison against the DAC variant.
  • Combination research alongside GHRP-class peptides such as Ipamorelin, where GHRH and ghrelin-receptor pathways are studied together.
  • Downstream IGF-1 and body-composition markers.

Clinical outlook

Human data on this specific compound is thin, and we would rather say so than overstate it. A Phase 2 trial studied CJC-1295 in HIV patients with visceral obesity but was terminated (NCT00267527), so it did not produce the evidence a completed study would have. The broader GHRH-analog approach, however, is well validated — Tesamorelin, another GHRH analog, completed Phase 3 trials and reached FDA approval. That makes the class credible even where this particular molecule remains early, and it is the gap researchers working with Mod GRF 1-29 are positioned to help close.

Frequently asked questions about CJC-1295 (no DAC / Mod GRF 1-29)

Straight answers to the questions researchers most often ask. Everything below summarizes published preclinical and clinical literature; it is not medical advice, and these compounds are supplied for laboratory research only.

What is CJC-1295?

CJC-1295 is a synthetic 29-amino-acid analog of growth-hormone-releasing hormone (GHRH 1–29) with four amino-acid substitutions that resist enzymatic breakdown. Our product is the "no DAC" form, also called Mod GRF (1–29).

What is the difference between CJC-1295 with DAC and without DAC?

DAC (drug affinity complex) is a lysine-linked group that binds albumin and extends the half-life from minutes to about a week. Without DAC the peptide produces a short, pulse-like GH release; with DAC it produces continuous elevation. They are studied for different questions.

How does CJC-1295 work?

It binds the pituitary GHRH receptor and stimulates release of the body's own growth hormone, raising IGF-1 downstream. It does not supply growth hormone directly.

Has CJC-1295 been tested in humans?

Only in limited studies. A Phase 2 trial in HIV-associated visceral obesity was terminated before completion, and early pharmacokinetic studies exist for the DAC form. Human data on the no-DAC form specifically is thin.

Is CJC-1295 FDA approved?

No. It is supplied for laboratory research only. Tesamorelin is the GHRH analog that did complete development and win approval.

Why is CJC-1295 paired with Ipamorelin in research?

Because GHRH-receptor and ghrelin-receptor stimulation are additive: Ipamorelin triggers the pulse, CJC-1295 amplifies it. The pairing is one of the most common designs in growth-hormone-axis research.

References

  1. Teichman SL, Neale A, Lawrence B et al. 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 The Journal of clinical endocrinology and metabolism, 2006
  2. Sackmann-Sala L, Ding J, Frohman LA et al. Activation of the GH/IGF-1 axis by CJC-1295, a long-acting GHRH analog, results in serum protein profile changes in normal adult subjects Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society, 2009
  3. Ionescu M, Frohman LA Pulsatile secretion of growth hormone (GH) persists during continuous stimulation by CJC-1295, a long-acting GH-releasing hormone analog The Journal of clinical endocrinology and metabolism, 2006
  4. Alba M, Fintini D, Sagazio A et al. Once-daily administration of CJC-1295, a long-acting growth hormone-releasing hormone (GHRH) analog, normalizes growth in the GHRH knockout mouse American journal of physiology. Endocrinology and metabolism, 2006
  5. Memdouh S, Gavrilović I, Ng K et al. Advances in the detection of growth hormone releasing hormone synthetic analogs Drug testing and analysis, 2021