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Published Phase 1 human studies

CJC-1295

CJC-1295

CJC-1295 is an investigational growth-hormone-releasing peptide that is not FDA-approved; this page explains what it is, how the DAC and no-DAC (mod GRF 1-29) forms differ in half-life, and the safety signals to know — while the mg-to-units math lives on the CJC-1295 dosage calculator.

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50units
0.5 mL5 mg/mL2.5 mg / dose
1 mL syringe - 100 u/mLFits
50 u050100 u
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10 mg
4
0 mg
28 days
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Formula and source context only. Not medical advice; verify with a clinician, product label, pharmacist, or approved research protocol. Do not use this tool to infer sterility, potency, purity, stability, compatibility, or an appropriate dose. Catalog and supply-chain data: finnrick.com/products - research date 2026-06-24.

CJC-1295: reference record

CJC-1295 - regulatory status, route, frequency and published range
Regulatory statusInvestigational; not FDA-approved
RouteSubcutaneous (CJC-1295 with DAC in cited study)
Dosing frequencySingle or study-scheduled
Published range30–60 mcg/kg
Evidence basisPublished Phase 1 human studies
Common vial sizes5, 10 (DAC / no-DAC)

Sources

  • PubMed - PMID 16352683Basis for the regulatory status, route, frequency and published range in the table above. Source last checked 2026-06-24

What is CJC-1295?

CJC-1295 is an investigational growth-hormone-releasing peptide. It exists in two forms that behave differently: the DAC version, which binds to albumin and persists far longer in circulation, and the no-DAC form often sold as mod GRF 1-29, which clears quickly.

Is CJC-1295 FDA-approved?

No. CJC-1295 is investigational and not FDA-approved. The published human data come from early-phase studies rather than from an approved product label, so there is no approved formulation or indication.

How is CJC-1295 given?

The cited human study used the DAC form subcutaneously, on a single or study-scheduled basis. There is no approved outpatient route or regimen, and the two forms are not interchangeable.

What are the known safety concerns with CJC-1295?

Data are limited. The FDA has noted serious adverse events associated with this substance, including increased heart rate and vasodilatory reactions. Nothing here establishes that any route or amount is safe.

Healthy-adult studies examined 30 and 60 mcg/kg among ascending doses; protocol-controlled

Weight-based conversion supported mathematically, but CJC-1295 with DAC must not be confused with 'no-DAC' products.

Limited data; FDA notes serious adverse events including increased heart rate and vasodilatory reaction.

Supply-chain quality · Finnrick

Avg quality score

5

/10

Purity range

68.75

99.95

%

Qty divergence

±

100

%

Vendors · samples

49

·

266

Common vial sizes

5, 10 (DAC / no-DAC)

mg

Test window

Dec 2024 - May 2026

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