Le contenu des preuves est maintenu en anglais.

Bottom line

A marketed growth-hormone-axis combination pairing a substance labeled “CJC-1295 (no DAC)” with GHRP-2 (pralmorelin), a hexapeptide ghrelin-receptor agonist. GHRP-2 has an approved product-specific diagnostic role in Japan, but no published controlled study of this combination was identified.

No established or recommended human dose.

Name and formulation variability

Market observation (source/date)Claimed components and amountsExact identity independently verified?Verification limits
Online-market listings observed in 2026Substance labeled “CJC-1295 (no DAC)” plus GHRP-2; variable amountNoSeller-declared identity and amount are not independent verification

Also known as: CJC-1295/GHRP-2, Mod GRF 1-29/GHRP-2, CJC-1295+ GHRP-2. GHRP-2: Pralmorelin (INN), GPA-748, KP-102.

Critical ambiguity: the clinical-study name CJC-1295 refers to the DAC conjugate designed for albumin binding. Online-market “CJC-1295 no DAC” usually refers to Modified GRF 1-29, a different substance. Evidence for CJC-1295 DAC cannot be transferred to Modified GRF 1-29 or this blend.

Exact identities and status
CJC-1295 and GHRP-2 identity and status do not transfer to the market blendA no-DAC marketed substance is separated from the different with-DAC identity. GHRP-2 has separate human evidence and product-specific diagnostic status in Japan; dotted links meet only at a market blend with no combination study.CJC-1295 NO DACmarketed substanceCJC-1295 WITH DACdifferent identityNOT INTERCHANGEABLEGHRP-2 / PRALMORELINseparate humanstudy evidenceJapan diagnosticproduct statusMARKET BLENDNO PUBLISHED COMBINATION STUDYIDENTITYHYPOTHESIZED / SHARED DOMAINMARKET ASSOCIATIONEVIDENCE GAP
Japan's pralmorelin status is product, jurisdiction, and indication specific. Legend: solid outlines identify the substances described on the page; dashed lines show hypothesized or shared biological domains; dotted lines show market association only; barred lines mark missing combination or compatibility evidence.
Alternative textuelle

The marketed CJC-1295 no-DAC substance is a different identity from clinical-studied CJC-1295 with DAC. GHRP-2 or pralmorelin has separate small human-study evidence and a product-specific diagnostic status in Japan. Neither status nor separate evidence authorizes or tests the market blend.

Component evidence

ComponentSeparate evidenceCombination evidenceCompatibility
CJC-1295 no DACHuman evidence: no controlled study identified. Regulatory record: no product-specific authorization identified. Limitations: GHRH-receptor/cAMP activity is inferred from sequence and class rather than demonstrated for this standalone substance.Not identifiedNo published stability data
GHRP-2 / pralmorelinHuman evidence: small, indication-specific studies measured GH-axis, pituitary-hormone, and food-intake endpoints. Regulatory record: PMDA lists a pralmorelin hydrochloride diagnostic product in Japan. Limitations: the product, jurisdiction, and diagnostic indication do not transfer to this blend.Not identifiedNot identified

The component evidence is limited and indication-specific. Arvat et al. studied six young adults and six older adults given GHRP-2 or hexarelin at 1 or 2 mcg/kg and reported GH release plus small ACTH, cortisol, and prolactin responses. Laferrère et al. used a randomized within-subject comparison in seven lean healthy men; a 270-minute GHRP-2 infusion at 1 mcg/kg/hour increased food intake by 35.9% versus saline. Neither study tested Modified GRF(1-29), CJC-1295, or this blend.

Combination-specific studies

A targeted PubMed search through 2026-08-06 identified no published human or controlled animal study of the specific CJC-1295 + GHRP-2 combination.

Safety and interaction uncertainties

  • GHRP-2 elevates ACTH, cortisol, and prolactin — confounding GH-axis readouts

  • Appetite stimulation may confound metabolic studies

  • No combination-specific safety data

  • Theoretical mitogenic concern from sustained GH/IGF-1 elevation

Regulatory and product-quality notes

  • Neither component FDA-approved for therapeutic use

  • PMDA lists GHRP Kaken 100 (pralmorelin hydrochloride), approved in Japan for diagnosis of growth-hormone secretory deficiency; this product-specific diagnostic authorization does not apply to the blend

  • The 2026 List explicitly names CJC-1295 among GHRH analogues and GHRP-2 (pralmorelin) among GH-releasing peptides in section S2.2.4; both are prohibited at all times

  • An online “research use only” label is not authorization for human use

Evidence gaps

  • No combination study (human or animal)

  • No dose-ratio optimisation data

  • No long-term safety data for the combination

  • Corticosteroid elevation complicates interpretation of any study using this blend

For jurisdiction context, see Japan regulation. Compare CJC-1295 + Ipamorelin and CJC-1295 + GHRP-6; the WADA page addresses the independent sport-status axis.

Sources

  1. Teichman SL, et al. Prolonged stimulation of GH and IGF-I secretion by CJC-1295. J Clin Endocrinol Metab. 2006;91(3):799-805. PMID 16352683. https://pubmed.ncbi.nlm.nih.gov/16352683/

  2. Pihoker C, et al. Pharmacokinetics and pharmacodynamics of GHRP-2 in children. J Clin Endocrinol Metab. 1998;83(4):1168-1172. PMID 9543135. https://pubmed.ncbi.nlm.nih.gov/9543135/

  3. Arvat E, et al. Effects of GHRP-2 and hexarelin, two synthetic GH-releasing peptides, on GH, prolactin, ACTH and cortisol levels in man. Peptides. 1997;18(6):885-891. PMID 9285939. https://pubmed.ncbi.nlm.nih.gov/9285939/

  4. Laferrère B, et al. Growth hormone-releasing peptide-2 (GHRP-2), like ghrelin, increases food intake in healthy men. J Clin Endocrinol Metab. 2005;90(2):611-614. PMID 15699539. https://pubmed.ncbi.nlm.nih.gov/15699539/

  5. Pharmaceuticals and Medical Devices Agency. GHRP Kaken 100 (pralmorelin hydrochloride), current product information and package insert. https://www.pmda.go.jp/PmdaSearch/rdDetail/iyaku/7223407D2023_1?user=1

  6. World Anti-Doping Agency. 2026 Prohibited List, section S2.2.4. https://www.wada-ama.org/sites/default/files/2025-09/2026list_en_final_clean_september_2025.pdf

Voix d'experts

Ce que disent les experts

Les commentaires sont des opinions et ne font pas partie de l'examen des preuves ; leur inclusion ne vaut pas approbation.

Aucun commentaire d’expert vérifié n’a été trouvé pour ce composé dans les sources acceptées par cet atlas — littérature évaluée par les pairs, communications universitaires, hospitalières et de sociétés médicales, autorités réglementaires, et journalisme scientifique signé.

L’absence de commentaire ne constitue pas une preuve pour ou contre le composé.

Les affirmations émanant de fournisseurs, cliniques et médias sociaux sont exclues par politique et ne sont pas comptées comme commentaires.

Aucune vidéo d’expert vérifiée n’a été trouvée pour ce composé dans les sources de cet atlas.

L’absence de vidéo ne constitue pas une preuve pour ou contre le composé.

Les vidéos de fournisseurs et de médias sociaux sont exclues par politique et ne sont pas comptées.

Questions

What does the marketed CJC-1295 plus GHRP-2 blend contain?

Listings pair GHRP-2 with a substance labeled CJC-1295 no DAC, usually meaning Modified GRF 1-29. The no-DAC substance is not the clinical-studied CJC-1295 DAC conjugate.

Has CJC-1295 plus GHRP-2 been studied as a combination?

No published human randomized trial or controlled animal study of the specific pair was identified. The available human findings concern GHRP-2 separately.

What safety uncertainties apply to CJC-1295 plus GHRP-2?

No combination-specific or long-term safety evidence was identified. Separate GHRP-2 studies measured additional pituitary hormones and food-intake effects, which complicates transferring isolated GH-axis observations to a blend claim.

Does Japan's pralmorelin diagnostic product authorize the marketed blend?

No. The PMDA record is specific to a pralmorelin hydrochloride product, Japan, and a diagnostic indication; it does not authorize a CJC-1295 combination or transfer to seller-declared material.

Has the no-DAC substance been tested in controlled human studies?

No controlled human study of the standalone no-DAC substance was identified on this page. Findings for the CJC-1295 DAC conjugate concern a different chemical identity.

Can hormone-release findings establish a clinical benefit from this pair?

No. Hormone release is a physiologic or surrogate endpoint, while clinical benefit from the exact combination requires its own controlled evidence.