About Mod GRF 1-29
Modified GHRH analog; binds GHRH receptors with improved stability to produce physiological GH pulses when combined with a GHRP
Mod-GRF 1-29 (also designated CJC-1293 without DAC, or tetrasubstituted GHRH[1-29]) is a synthetic analogue of the first 29 amino acids of growth hormone-releasing hormone, modified at four positions including substitution of norleucine at position 27 to improve proteolytic stability and extend the effective half-life of native GHRH 1-29, thereby producing more sustained pituitary GH stimulation per dose. Like endogenous GHRH, it acts through GHRH receptors on pituitary somatotrophs to stimulate cAMP-mediated GH synthesis and secretion, and is administered to mimic the hypothalamic pulse signal that drives GH release and downstream IGF-1 axis activity. Modified GHRH 1-29 analogues sharing the core amino acid substitutions of Mod-GRF 1-29, specifically [Nle27]GHRH(1-29)-NH2, have been administered to humans in controlled studies that documented sustained GH and IGF-1 axis effects with endocrine, metabolic, and immune endpoints characterized in age-advanced subjects. Mod-GRF 1-29 has not received FDA approval; the related compound sermorelin (unmodified GHRH 1-29) was previously FDA-approved for pediatric GH deficiency but was withdrawn by its manufacturer, and Mod-GRF 1-29 is an investigational compound not approved for any clinical indication. Naming note — Mod GRF 1-29 vs CJC-1295: the research compound marketplace uses several overlapping names for this compound. "Mod GRF 1-29" and "CJC-1295 without DAC" refer to the same tetrasubstituted GHRH(1-29) peptide. "CJC-1295 with DAC" (or simply "CJC-1295" in most clinical protocol contexts) is a different compound — it includes a Drug Affinity Complex (DAC) linker that enables albumin binding and produces a dramatically extended half-life (~8 days vs ~30 minutes for Mod GRF 1-29). CJC-1295 with DAC is used as an infrequent injection (weekly or biweekly) while Mod GRF 1-29 / CJC-1295 without DAC is used at each injection session, typically immediately before or alongside a GHRP such as ipamorelin to maximally leverage the GH pulse window. Dosage in research protocols: Mod GRF 1-29 is typically used at 100 mcg per injection alongside ipamorelin or another GHRP, administered 2–3 times daily or immediately before sleep to align with natural GH secretion peaks. Subcutaneous injection after reconstitution with bacteriostatic water is the standard route. Provider availability for Mod GRF 1-29 and CJC-1295 compounds is listed in the PeptideBase directory.
Mod GRF 1-29 Benefits & Research Areas
Research Signals
Commonly researched in the context of
Population research notes
These signals reflect research interest areas, not treatment indications.
Regulatory & Evidence
Risk Profile
Moderate risk profile in research contexts. Review contraindications and administration guidelines before use.
Regulatory Status
- Availability Status
- Research Only
- FDA Status
- Not Evaluated
GHRH analog (CJC-1295 without DAC). Related to sermorelin but structurally distinct (tetrasubstituted AAs). No FDA approval. Not on FDA 503A bulks list. WADA prohibited. Research chemical.
Regulatory status reflects publicly available information and may change. This is not legal or medical advice.
Research Sources
2 sources cited · 1 strong · 1 moderate
2 RCTs
Endocrine and metabolic effects of long-term administration of [Nle27]growth hormone-releasing hormone-(1-29)-NH2 in age-advanced men and women
Journal of Clinical Endocrinology and Metabolism · 1997
Research in a 5-month randomized placebo-controlled trial found that nightly subcutaneous administration of a GHRH(1-29) analog significantly increased 12-hour integrated GH levels, serum IGF-I, and IGFBP-3, with increases in lean body mass in men, improved skin thickness in both sexes, and enhanced insulin sensitivity and well-being in men.
Effects of [norleucine27]growth hormone-releasing hormone (GHRH) (1-29)-NH2 administration on the immune system of aging men and women
Journal of Clinical Endocrinology and Metabolism · 1997
Research in a randomized controlled trial found that 4-month nightly GHRH analog administration significantly increased GH secretion and IGF-I levels while also enhancing immune cell activation, including B cell numbers, T cell receptor expression, and interleukin-2 responsiveness in elderly men and women, without sex differences in immune response.
Mod GRF 1-29 Side Effects & Safety Considerations
Moderate risk profile. Review all reported considerations carefully before use.
Reported contraindications & considerations
Consult a qualified healthcare professional before making any health decisions. This information is educational only and does not constitute medical advice.
Known Interactions
1 notedResearch suggests Ipamorelin and Mod GRF 1-29 may produce enhanced growth hormone pulse effects when combined. Ipamorelin acts via ghrelin receptors (GHSR) while Mod GRF 1-29 acts via GHRH receptors — distinct pathways that research suggests may amplify GH secretion when activated together.
Raun K et al. (1998) Ipamorelin, the first selective growth hormone secretagogue. Eur J Endocrinol; Bowers CY et al. (1991) Synergism of GHRH and GHRP. Endocrinology
These interactions reflect published research and are provided for educational purposes only. This is not medical advice. Consult a qualified healthcare professional before combining any compounds or medications.
Research Stacks
Browse all →Where to Buy Mod GRF 1-29 — Providers & Availability
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Questions to Ask Your Provider
Frequently Asked Questions — Mod GRF 1-29
Mod-GRF 1-29 (also designated CJC-1293 without DAC, or tetrasubstituted GHRH[1-29]) is a synthetic analogue of the first 29 amino acids of growth hormone-releasing hormone, modified at four positions including substitution of norleucine at position 27 to improve proteolytic stability and extend the effective half-life of native GHRH 1-29, thereby producing more sustained pituitary GH stimulation per dose. Like endogenous GHRH, it acts through GHRH receptors on pituitary somatotrophs to stimulate cAMP-mediated GH synthesis and secretion, and is administered to mimic the hypothalamic pulse signal that drives GH release and downstream IGF-1 axis activity.
pituitary GHRH receptor agonism — pulsatile GH stimulation, improved proteolytic stability vs native GHRH 1-29, synergistic GH release when combined with GHRPs (ipamorelin, GHRP-6), ~30 min half-life — requires dosing at each session vs CJC-1295 with DAC (weekly).
Research on Mod GRF 1-29 primarily documents effects related to pituitary GHRH receptor agonism — pulsatile GH stimulation and improved proteolytic stability vs native GHRH 1-29 and synergistic GH release when combined with GHRPs (ipamorelin, GHRP-6) and ~30 min half-life — requires dosing at each session vs CJC-1295 with DAC (weekly). These are areas covered in preclinical and clinical literature — individual response varies and effects depend on context of use.
Reported contraindications and considerations for Mod GRF 1-29 include active cancer, acromegaly. This is educational information only — consult a qualified healthcare professional before use.
13 providers in the directory currently offer Mod GRF 1-29.
Research in a 5-month randomized placebo-controlled trial found that nightly subcutaneous administration of a GHRH(1-29) analog significantly increased 12-hour integrated GH levels, serum IGF-I, and IGFBP-3, with increases in lean body mass in men, improved skin thickness in both sexes, and enhanced insulin sensitivity and well-being in men.
Mod GRF 1-29 is featured in the following research stacks on PeptideBase: Hexarelin + Mod GRF 1-29: Anabolic GH Amplification.