CJC-1295 + GHRP-2 Blend
Also known as: CJC/GHRP-2, Potent GH Stack, Mod GRF 1-29 + GHRP-2, CJC-1295 no DAC + GHRP-2
Evidence: Preclinical
Overview
Vial blend of CJC-1295 without DAC (Mod GRF 1-29) and GHRP-2 (pralmorelin), 5 mg each; GHRP-2 raised GH and appetite in human studies, and no study has tested the pair.
Vendors in the catalog sell this as CJC-1295 without DAC (Mod GRF 1-29) and GHRP-2, 5 mg each. Mod GRF 1-29 has no published study of its own, and its D-Ala2 substitution only extends the half-time of GHRH(1-29) to about 7 min in men (Soule 1994). GHRP-2 is a synthetic hexapeptide ghrelin-receptor agonist approved in Japan only as a single-dose diagnostic for GH deficiency (Chihara 2007); it sustained GH and IGF-1 over a 30-day infusion in older adults and increased food intake 36% in healthy men. IV GHRP-2 given with GHRH was synergistic in children (Pihoker 1995), the rationale for the pairing, but no study has tested this blend. FDA lists injectable GHRP-2 in category 2 for 503B outsourcing and CJC-1295 in the withdrawn-nomination table of its compounding safety-risk page.
Benefits
GH release (human, GHRP-2); increased food intake (human, GHRP-2 infusion); GH release by Mod GRF 1-29 inferred from related GHRH analogs; body-composition and recovery claims untested for the blend
Dosing reference
- Research dose
- 200 to 500 mcg of blend per injection (100 to 250 mcg of each at the 5 mg/5 mg ratio), 1 to 3x daily: vendor/community range, no published human dose of the blend or of Mod GRF 1-29
- Range
- 200 to 500 mcg, 1-3x daily
- Reconstitution
- 2 mL bacteriostatic water
- Common vial sizes
- 10 mg
Subcutaneous in community use, usually fasted. Human GHRP-2 doses: 1 mcg/kg or 100 mcg IV (diagnostic), 1 mcg/kg/h by continuous SC infusion for 30 days in older adults, and 0.3 to 3 mcg/kg/day SC in GH-deficient children. No human dose of Mod GRF 1-29 has been published. The 5 days on, 2 days off pattern is community convention.
Mechanism
Proposed, from component and class studies. Mod GRF 1-29 is a tetrasubstituted GHRH(1-29) analog acting on the pituitary GHRH receptor; its activity has not been measured directly. GHRP-2 activates the ghrelin receptor (GHS-R1a), raising GH within 60 min, and in swine it also raised ACTH and cortisol where ipamorelin did not (Raun 1998). GHRH-receptor and ghrelin-receptor agonists given together raise GH more than either alone, shown for IV GHRP-2 with GHRH in children (Pihoker 1995). GHRP-2's ghrelin-like action also fits the rise in food intake seen with continuous infusion (Laferrere 2005).
Evidence
Preclinical: animal or in vitro data only
- D-Ala2 substitution, one of Mod GRF 1-29's four changes, raised the plasma half-time of GHRH(1-29) from 4.3 to 6.7 min in 10 normal men (Soule et al., 1994)
- IV GHRP-2 1 mcg/kg in 10 children gave a predictable GH rise with a plasma half-life of 33 min (Pihoker et al., 1998)
- 30-day continuous SC infusion at 1 mcg/kg/h sustained pulsatile GH and raised IGF-1 in 17 older adults (Bowers et al., 2004)
- SC GHRP-2 infusion increased ad libitum food intake 36% in 7 healthy men (Laferrere et al., 2005)
- Human-trial status: no study has tested the blend as sold, and none has tested Mod GRF 1-29 itself. GHRP-2 is approved in Japan only as a GH-deficiency diagnostic (Chihara et al., 2007); IV GHRP-2 plus GHRH, not Mod GRF 1-29, was synergistic in children (Pihoker et al., 1995)
References
- Incorporation of D-Ala2 in growth hormone-releasing hormone-(1-29)-NH2 increases the half-life and decreases metabolic clearance in normal men. Soule S, King JA, Millar RP, Journal of Clinical Endocrinology & Metabolism, 1994
- 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 analog. Jette L, Leger R, Thibaudeau K, et al., Endocrinology, 2005
- Pharmacokinetics and pharmacodynamics of growth hormone-releasing peptide-2: a phase I study in children. Pihoker C, Kearns GL, French D, Bowers CY, Journal of Clinical Endocrinology & Metabolism, 1998
- Diagnostic studies with intravenous and intranasal growth hormone-releasing peptide-2 in children of short stature. Pihoker C, Middleton R, Reynolds GA, Bowers CY, Badger TM, Journal of Clinical Endocrinology & Metabolism, 1995
- Sustained elevation of pulsatile growth hormone (GH) secretion and insulin-like growth factor I (IGF-I), IGF-binding protein-3 (IGFBP-3), and IGFBP-5 concentrations during 30-day continuous subcutaneous infusion of GH-releasing peptide-2 in older men and women. Bowers CY, Granda R, Mohan S, Kuipers J, Baylink D, Veldhuis JD, Journal of Clinical Endocrinology & Metabolism, 2004
- Growth hormone releasing peptide-2 (GHRP-2), like ghrelin, increases food intake in healthy men. Laferrere B, Abraham C, Russell CD, Bowers CY, Journal of Clinical Endocrinology & Metabolism, 2005
- A simple diagnostic test using GH-releasing peptide-2 in adult GH deficiency. Chihara K, Shimatsu A, Hizuka N, Tanaka T, Seino Y, Kato Y; KP-102 Study Group, European Journal of Endocrinology, 2007
- Ipamorelin, the first selective growth hormone secretagogue. Raun K, Hansen BS, Johansen NL, et al., European Journal of Endocrinology, 1998
Side effects
No human safety study of the blend or of Mod GRF 1-29 has been published. A 30-day continuous GHRP-2 infusion kept safety screening tests normal in 17 older adults (Bowers 2004). GHRP-2 raised ACTH and cortisol in swine (Raun 1998) and increased hunger in men. Commonly reported by users (anecdotal): water retention, hunger, tingling in the hands and joint aches. CJC-1295 with DAC, a different product, has a half-life of 5.8 to 8.1 days, so mixing up the two forms changes exposure a great deal. Injectable and nasal GHRP-2 is in category 2 of FDA's 503B interim policy (added 2023-09-29), and CJC-1295 is in the withdrawn-nomination table for 503A, as of 2026-04-22: https://www.fda.gov/drugs/human-drug-compounding/certain-bulk-drug-substances-use-compounding-may-present-significant-safety-risks. FDA cites serious adverse events with CJC-1295, including increased heart rate and a systemic vasodilatory reaction.
Storage
- Storage
- Refrigerate 2-8°C (36-46°F)
- Lyophilized
- 2+ years at room temp, 3+ years refrigerated
- Reconstituted
- 28-30 days refrigerated
Pharmacology
- Half-life
- Mod GRF 1-29 not measured; D-Ala2-GHRH(1-29) ~6.7 min (human, IV). GHRP-2 ~33 min (children, IV bolus). The ~30 min figure for Mod GRF is community lore
- Bioavailability
- Not measured for Mod GRF 1-29. GHRP-2 raised GH after SC and intranasal dosing in humans; absolute bioavailability not reported. No data for the blend