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SYS · ONLINEPASS · 63.0%
Open Assay
Independent Testing / Est. 2026
BATCH04·26·B
PASS63.0%
N27
PeptidesBlend, GH-stackCJC-1295 + Ipamorelin (Blend)

CJC-1295 + Ipamorelin (Blend)

/ Two-component vendor blend — CJC-1295 (with or without DAC; vendors vary) plus ipamorelin (selective GHS-R1a hexapeptide)
SPECULATIVEN = 0 · TESTING PENDING

ALIAS · CJC-1295/Ipamorelin · Mod-GRF + Ipamorelin · IPA/CJC blend · Classic GH stack

Pass rate
0
Samples
0
Suppliers
Research use onlyAny dose figures below describe what specific cited studies used, reported factually. Nothing on this page is guidance for human use.READ FIRST →

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§ A · Identity
Primary sequence— sequence not captured —
MW · CLASS · Two-component vendor blend — CJC-1295 (with or without DAC; vendors vary) plus ipamorelin (selective GHS-R1a hexapeptide)CATEGORY · Blend, GH-stack

Tier 4 for the combination. Each component independently has the evidence reviewed under its own peptide page. The blend has no published combination pharmacology trial. The most-discussed peptide stack on research-vendor and bodybuilding forums.

§ B · Mechanism of action

The pharmacological rationale is convergent stimulation of pituitary GH release through two receptor pathways — CJC-1295 via the GHRH receptor and ipamorelin via the ghrelin (GHS-R1a) receptor. In animal pharmacology, GHRH agonist plus GHS-R1a agonist produces synergistic GH peaks compared with either alone; the principle is established class biology, but no published human trial of this specific combination exists.

§ C · Human clinical evidence

None for the combination. Component evidence: CJC-1295 with DAC has a single 2006 Phase 1 study (tier 4); CJC-1295 without DAC has no published clinical data; ipamorelin reached Phase 2 in postoperative ileus and orthopedic recovery without clear efficacy translation.

§ F · Safety signal

No combined safety database. Each component carries minimal individual human safety data (CJC-1295 with DAC has Phase 1 only; ipamorelin Phase 2 short-term only). Predicting combined effects from components is inference, not data.

§ H · Regulatory status

Regulatory status

FDA status:
Not FDA-approved
§ I · Notable gaps and controversies

Vendor presentations of CJC-1295/Ipamorelin as an established 'protocol' are not supported by clinical-trial evidence at the dose ratios or schedules typically marketed. The pharmacological rationale is sound; the human safety and efficacy database is essentially empty.