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Growth Hormone Axis

CJC-1295 With DAC calculator

The long-acting form of CJC-1295, bound to a drug affinity complex that extends its half-life to about a week. Not approved; prohibited in sport.

Also known as: CJC-1295 DAC, Drug Affinity Complex CJC

FDA status — not an approved drug Not FDA-approved for any use. CJC-1295 was placed in Category 2 of FDA's bulk drug substances list. Prohibited in sport by WADA.

80 units
on a 100-unit syringe
0.8 mL
volume drawn
2.5 mg/mL
concentration
2 doses
per vial
050100

Schedule CJC-1295 With DAC → Set your dosing schedule and get a phone notification when each dose is due. Free.

A worked example

A 5 mg vial reconstituted with 2 mL of bacteriostatic water gives 2.5 mg/mL. A 2000 mcg dose is then 0.8 mL — about 80 units on a 100-unit insulin syringe, giving roughly 2 doses per vial before accounting for residual volume left in the vial and syringe.

Prefer paper? Download the printable CJC-1295 With DAC dosing chart (PDF) — every vial size and water volume in syringe units, with the same review byline as this page. All charts →

Commonly cited dose range

Figures circulating for CJC-1295 With DAC run from 1000 mcg to 4000 mcg. The DAC form is long-acting and dosed weekly rather than daily. Figures reflect community reference amounts in micrograms. There is no established or approved dose.

Read this as reference information, not instruction. These numbers describe what is commonly discussed, not what is right for any individual. Dose, frequency, and whether to use CJC-1295 With DAC at all are decisions for a licensed clinician who knows your history.

Common questions

What's the difference between CJC-1295 with and without DAC?

The DAC (drug affinity complex) version binds albumin in the blood, extending its half-life to roughly a week, so it is dosed weekly. The no-DAC form clears in hours and is dosed daily. Neither is approved.

Is the DAC form safe?

It produces sustained, non-pulsatile elevation of growth hormone and IGF-1, which differs from the body's natural pattern and raises concerns about insulin resistance and fluid retention. Development was discontinued after a safety event in one trial.

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