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MUSCLE & GROWTHPEPTIDE PROFILE

Mod GRF 1-29

Also known as Modified GRF 1-29, CJC-1295 without DAC, CJC-1295 no DAC, Tetrasubstituted GRF 1-29

Mod GRF 1-29 (Modified Growth Hormone Releasing Factor 1-29) is a stabilized synthetic analog of endogenous GHRH with four amino acid substitutions that resist enzymatic degradation. Unlike CJC-1295 with DAC, it lacks the Drug Affinity Complex and has a short 30-minute half-life, producing pulsatile GH release that closely mimics natural physiology. It is almost always co-administered with a GHRP such as ipamorelin.

Last updated June 25, 2026

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Mod GRF 1-29: quick citable summary

Mod GRF 1-29 is listed by PeptaHub as a muscle & growth peptide with a research only legal-status classification. The page summarizes mechanism, research context, common routes, safety notes, and references for writers and AI answer engines.

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PeptaHub. “Mod GRF 1-29: Mechanism, Research Context, Safety.” peptahub.com, 2026. https://peptahub.com/peptides/mod-grf-1-29. Licensed CC BY 4.0.

License: Creative Commons Attribution 4.0 International. Link back to https://peptahub.com/peptides/mod-grf-1-29.

SAMEAS / EXTERNAL IDS
Mod GRF 1-29 CAS: 863288-34-0
QUICK ANSWER

What is Mod GRF 1-29?

Mod GRF 1-29 is a stabilized GHRH analog with four amino acid substitutions that resist enzymatic degradation, intended to produce pulsatile GH release. It is usually paired with a GHRP like ipamorelin. No human trial of Mod GRF 1-29 itself has been published.

§ 01

Overview

Mod GRF 1-29 (Modified Growth Hormone Releasing Factor 1-29) is a stabilized synthetic analog of endogenous GHRH with four amino acid substitutions that resist enzymatic degradation. Unlike CJC-1295 with DAC, it lacks the Drug Affinity Complex and has a short 30-minute half-life, producing pulsatile GH release that closely mimics natural physiology. It is almost always co-administered with a GHRP such as ipamorelin.

§ 02

Mechanism of action

Mod GRF 1-29 binds to and activates GHRH receptors on somatotroph cells of the anterior pituitary. The four amino acid substitutions (at positions 2, 8, 15, and 27) protect against dipeptidyl peptidase-IV cleavage and other serum proteases, extending bioactive duration beyond native GHRH (1-29) while maintaining pulsatility. Receptor activation triggers Gs-mediated adenylyl cyclase signaling, elevating intracellular cAMP, which drives GH synthesis and secretion. The resulting GH pulse stimulates hepatic IGF-1 production, skeletal muscle protein synthesis via IGF-1R/PI3K/Akt/mTOR pathways, lipolysis in adipose tissue via hormone-sensitive lipase activation, and collagen synthesis in connective tissue. Peak GH levels occur approximately 30 minutes post-injection, returning to baseline within 2–3 hours, preserving normal GH pulsatility over time.

§ 03

Reported study ranges

PurposeRouteReported rangeFrequency
GH pulse stimulation (combined with GHRP)subcutaneous100200 mcg1–3 times daily

Reported ranges are for research context only. Consult a qualified healthcare professional before using any peptide.

Convert Mod GRF 1-29 research-range units

Need to convert mg to mcg, dose volume, or U-100 syringe units? The Mod GRF 1-29 dose calculator is preloaded with these ranges, or use the general dose unit converter.

§ 04

Research summary

No published human trial has administered Mod GRF 1-29 itself. The human evidence cited for this peptide comes from studies of the DAC-modified analog CJC-1295 (Teichman et al., JCEM 2006; Ionescu & Frohman, JCEM 2006), which has a fundamentally different pharmacokinetic profile, and from the broader GHRH analog class such as sermorelin. The tetrasubstituted GHRH(1-29) backbone shared by both was shown to resist protease degradation in rats (Jetté et al., Endocrinology 2005). GHRH analogs and ghrelin mimetics such as ipamorelin produce greater-than-additive GH release when combined, an effect established for the drug classes rather than for this specific pairing. No human pharmacokinetic study, dose-response study, or body composition trial of Mod GRF 1-29 has been published as of 2026.[1][2][3][4][5]

📄This section cites 5 peer-reviewed sources. View all references →
§ 04b

Evidence grading

Each claimed benefit is graded by the strength of available evidence. Grades reflect study quality, not effect size.

preliminary
GH pulse stimulation via GHRH receptorGHRH receptor agonism is well established for the class, and Teichman et al. JCEM 2006 showed sustained GH and IGF-1 release in healthy adults. That study used CJC-1295 with DAC, not Mod GRF 1-29, so the human dose-response for this peptide is extrapolated rather than measured
preliminary
Synergy with GHRP co-administrationGHRH analogs plus ghrelin mimetics produce greater-than-additive GH release, a well-described class effect. No published study quantifies the amplification for Mod GRF 1-29 with ipamorelin specifically, and the commonly repeated 3-10x figure has no identifiable source
moderate
DPP-IV resistance extending active half-lifeJetté et al. Endocrinology 2005: tetrasubstituted GHRH(1-29) resisted protease degradation, demonstrated biochemically and in rats. No human pharmacokinetic study of Mod GRF 1-29 has been published
insufficient
Body composition and muscle gain benefitNo large-scale human efficacy trials for body composition endpoints completed as of 2026; anecdotal use only
preliminary
Reduced desensitization vs long-acting GHRH analogsIonescu & Frohman JCEM 2006 found GH secretion remained pulsatile during continuous stimulation by CJC-1295 in healthy men. The inference that a shorter half-life further reduces desensitization is theoretical and has not been benchmarked in humans

Strong = multiple RCTs · Moderate = limited trials or observational · Preliminary = animal or in vitro only · Insufficient = anecdotal or no published data

§ 05

Side effects

Injection site redness or swelling
Transient flushing
Headache
Dizziness
Water retention (with high doses)
Tingling or numbness (extremities, rare)
Increased hunger (especially combined with GHRP-6)

Side effects vary by individual. This is not an exhaustive list. Report unusual symptoms to a healthcare professional.

§ 06

Common stacks

Peptides commonly paired with Mod GRF 1-29 for synergistic effects.

§ 08

Sourcing & access

Research compound

Mod GRF 1-29 is classified as a research compound. Regulatory status varies by jurisdiction. Always verify current legal status and source from vendors providing third-party certificates of analysis (COA).

§ 09

Frequently asked questions

Mod GRF 1-29 (also called CJC-1295 without DAC) is a modified growth hormone releasing factor with four amino acid substitutions at positions 2, 8, 15, and 27 that protect against enzymatic degradation. Unlike CJC-1295 with DAC, it has a short 30-minute half-life, preserving natural GH pulsatility.

Mod GRF 1-29 activates GHRH receptors on pituitary somatotroph cells, triggering GH synthesis and secretion via cAMP signaling. The commonly quoted timing — a GH peak around 30 minutes and a return to baseline within 2-3 hours — reflects GHRH class pharmacology rather than a published pharmacokinetic study of this peptide, since none exists.

Side effects include injection site redness or swelling, transient flushing, headache, dizziness, water retention at high doses, and increased hunger when combined with GHRP-6. Mod GRF 1-29 was not among the 12 peptides the FDA removed from Category 2 in April 2026 and cannot legally be compounded in the US.

GHRH analogs and ghrelin mimetics act on different pituitary receptors, and giving both releases more GH than either alone. That synergy is established for the drug classes; no published study measures it for Mod GRF 1-29 with ipamorelin specifically, so figures like "3-10x" that circulate in community sources are not traceable to a trial. Ipamorelin is preferred among GHRPs because it has less effect on cortisol and prolactin.

§ 10

Research references

  1. Human growth hormone-releasing factor (hGRF)1-29-albumin bioconjugates activate the GRF receptor on the anterior pituitary in rats: identification of CJC-1295 as a long-lasting GRF analogJetté L, Léger R, et al.Endocrinology, 2005PubMed
  2. 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 adultsTeichman SL, Neale A, et al.Journal of Clinical Endocrinology and Metabolism, 2006ClinicalTrials.gov
  3. Pulsatile secretion of growth hormone (GH) persists during continuous stimulation by CJC-1295, a long-acting GH-releasing hormone analogIonescu M, Frohman LAJournal of Clinical Endocrinology and Metabolism, 2006PubMed
  4. Once-daily administration of CJC-1295, a long-acting growth hormone-releasing hormone (GHRH) analog, normalizes growth in the GHRH knockout mouseAlba M, Fintini D, et al.American Journal of Physiology — Endocrinology and Metabolism, 2006PubMed
  5. Advances in the detection of growth hormone releasing hormone synthetic analogsMemdouh S, Gavrilović I, Ng K, et al.Drug Testing and Analysis, 2021Review
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