Informational only. Not medical advice.INFORMATIONAL PLATFORM ONLY — NOT MEDICAL ADVICE, DIAGNOSIS, OR TREATMENT
Informational only. Not medical advice.INFORMATIONAL PLATFORM ONLY — NOT MEDICAL ADVICE, DIAGNOSIS, OR TREATMENT
Head-to-head comparison of CJC-1295 (no DAC) and Hexarelin — mechanism, side effects, legal status, and pricing.
CJC-1295 without Drug Affinity Complex (no DAC), also known as Modified GRF(1-29), is a synthetic analog of the first 29 amino acids of growth hormone-releasing hormone (GHRH). Four amino acid substitutions at positions 2, 8, 15, and 27 confer resistance to DPP-IV enzymatic degradation while maintaining GHRH-receptor binding activity. Unlike the DAC-conjugated variant (half-life 6–8 days via albumin binding), the no-DAC form has a short half-life of approximately 30 minutes, producing brief, pulsatile bursts of GH secretion. Not FDA-approved in any form.
Hexarelin (His-D-2MeTrp-Ala-Trp-D-Phe-Lys-NH2) is a synthetic hexapeptide growth hormone secretagogue developed by Mediolanum (Italy) in the 1990s. It is a potent ghrelin-receptor (GHSR-1a) agonist that also binds the CD36 scavenger receptor, giving it a cardioprotective signal distinct from other GHRPs. It is not FDA-approved for any indication and remains a research-only compound; its clinical development for GH deficiency and cardiac indications did not reach approval. A defining feature versus other GHRPs is rapid, pronounced tachyphylaxis with chronic daily dosing.
CJC-1295 (no DAC)
Hexarelin
Category
Legal Status
Mechanism
Half-life
COA-verified vendors · trust score ≥70 required · single-vial price — bulk/bundle deals may be lower
CJC-1295 (no DAC)
Hexarelin
COA corpus from Disclosed Labs — independently tested batches only.
CJC-1295 (no DAC)
2
COAs
99.4%
Avg purity
2
Labs
Hexarelin
10
COAs
99.4%
Avg purity
4
Labs
The parent molecule CJC-1295 (DAC form) was identified by Jetté et al. (Endocrinology, 2005; PMID 15817669) at ConjuChem as a tetrasubstituted GHRH(1-29) bioconjugate that covalently binds Cys34 of serum albumin via a maleimidopropionyl-lysine linker, extending half-life to roughly 5.8–8.1 days. In healthy adults, Teichman et al. (JCEM, 2006; PMID 16352683) showed single SubQ doses of the DAC form produced 2- to 10-fold GH elevations for ≥6 days and 1.5- to 3-fold IGF-1 elevations for 9–11 days, and Ionescu & Frohman (JCEM, 2006; PMID 17018654) demonstrated that pulsatile GH secretion was preserved (7.5-fold increase in trough GH, IGF-1 up 45%). ConjuChem halted Phase 2 lipodystrophy development around 2006–2007 after a participant death in an HIV-visceral-adiposity trial (deemed by the trial physician most likely due to pre-existing coronary artery disease rather than CJC-1295, but the program was not resumed; aidsmap news, July 2006). The no-DAC form described here ('Modified GRF 1-29') shares the same position-2/8/15/27 substitutions (which confer DPP-IV resistance; see Soule et al., JCEM 1994, PMID 7962295 for the foundational D-Ala2 half-life work) but omits the albumin-linker lysine, giving a short (~30 min) half-life similar to sermorelin. No form of CJC-1295 is FDA-approved for any indication. Grey-market compounding practice pairs the no-DAC form with ipamorelin; this combination is not clinically validated for anti-aging, body composition, or performance use, and peer-reviewed human trials of the no-DAC variant specifically are lacking — the 100–300 mcg dosing range reflects community practice, not clinical evidence.
Key references
CJC-1295 (no DAC) (Performance) and Hexarelin (Hormone) are in different categories and target different biological pathways. This is a common pattern in multi-compound research protocols. Researchers should monitor the biomarkers from both profiles and watch for interactions listed in each compound’s contraindications. Consult a licensed healthcare provider before combining any research compounds.
This platform provides informational tools only, not medical advice. This comparison is for educational purposes only. Consult a licensed provider.
Side Effects
Contraindications
Lab Testing
Ghigo et al. (1994, PMID 8126144, JCEM) characterized hexarelin's GH-releasing activity across IV, SubQ, intranasal, and oral routes in healthy men, establishing it as a potent GH secretagogue. Rahim & Shalet (1998, PMID 10990150, Growth Horm IGF Res) demonstrated that twice-daily SubQ hexarelin in healthy elderly subjects caused ~45% attenuation of the GH AUC over 16 weeks, with partial recovery 4 weeks after discontinuation — the canonical human tachyphylaxis study. Bodart et al. (2002, PMID 11988484, Circulation Research) showed that hexarelin's cardiovascular action in perfused hearts is mediated by CD36 rather than GHSR-1a and is absent in CD36-null animals. Hexarelin has never been FDA-approved; grey-market use for body composition, recovery, or cardiac benefit is not clinically validated.
Key references
Disclosed Labs