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 GHRP-2 — 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.
GHRP-2 (pralmorelin) is a synthetic hexapeptide ghrelin receptor agonist that stimulates pituitary growth hormone release. It is approved in Japan (Kaken Pharmaceutical, 2004) as a single-dose diagnostic agent for GH deficiency, but is NOT FDA-approved in the US and is research-only. Unlike ipamorelin, GHRP-2 is non-selective and modestly raises ACTH, cortisol, and prolactin.
CJC-1295 (no DAC)
GHRP-2
Category
Legal Status
Mechanism
Half-life
Side Effects
COA-verified vendors · trust score ≥70 required · single-vial price — bulk/bundle deals may be lower
CJC-1295 (no DAC)
GHRP-2
COA corpus from Disclosed Labs — independently tested batches only.
CJC-1295 (no DAC)
2
COAs
99.4%
Avg purity
2
Labs
GHRP-2
13
COAs
99.3%
Avg purity
6
Labs
GHRP-2 is among peptides under FDA review for the Category 1 (503A) list; if added, it would require a prescription to be compounded by registered 503A/503B pharmacies — not yet authorized. CJC-1295 (no DAC) remains research-only. In April 2026 the FDA removed 12 peptides from Category 2, which does not place them on the Category 1 list or authorize compounding. The FDA's Pharmacy Compounding Advisory Committee is advisory and meets July 23–24, 2026 to review nominations and make recommendations to the FDA.
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) and GHRP-2 are both in the Performance category and may have overlapping mechanisms. Researchers should review both profiles carefully, understand the mechanisms of action, and monitor the relevant biomarkers when combining compounds in the same class. As always, consult a licensed healthcare provider before making any decisions about combining research compounds.
This platform provides informational tools only, not medical advice. This comparison is for educational purposes only. Consult a licensed provider.
Contraindications
Lab Testing
GHRP-2 is approved in Japan (Kaken Pharmaceutical, 2004) as pralmorelin for single-dose diagnostic GH-stimulation testing; Chihara et al. (2007, PMID 17609397) validated a 100 mcg IV dose with a peak-GH <15 mcg/L cut-off against the insulin tolerance test. Arvat et al. (1997, PMID 9285939) showed GHRP-2 raises GH, prolactin, ACTH, and cortisol in healthy men, with hormonal effects similar to hexarelin. Laferrère et al. (2005, PMID 15699539) demonstrated that IV GHRP-2 significantly increases food intake in healthy men, consistent with its ghrelin-like activity. Pralmorelin review: Drugs R D 2004 (PMID 15230633). GHRP-2 is more potent than ipamorelin for raw GH output but is non-selective; grey-market anti-aging, muscle-gain, and performance use is not clinically validated in the US.
Key references
Disclosed Labs