O conteúdo das evidências é mantido em inglês.

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.
Alternativa em texto

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

Vozes de especialistas

O que dizem os especialistas

Os comentários são opiniões e não fazem parte da revisão de evidências; a inclusão não significa endosso.

Nenhum comentário de especialista verificado foi encontrado para este composto nas fontes que este atlas aceita — literatura revisada por pares, comunicações universitárias, hospitalares e de sociedades médicas, reguladores e jornalismo científico com autoria nominal.

A ausência de comentários não é evidência a favor ou contra o composto.

Alegações de fornecedores, clínicas e redes sociais são excluídas por política e não são contabilizadas como comentários.

Nenhum vídeo de especialista verificado foi encontrado para este composto nas fontes deste atlas.

A ausência de vídeos não é evidência a favor ou contra o composto.

Vídeos de fornecedores e redes sociais são excluídos por política e não são contabilizados.

Questões

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.