Dosage Schedule
| Cycle time | Amount per use | Frequency |
|---|---|---|
| Weeks 1–2 | 100 mcg | Once daily |
| Weeks 3–4 | 150 mcg | Once daily |
| Weeks 5–6 | 200 mcg | Once daily |
| Weeks 7–12 | 250–300 mcg | Once daily |
Reconstitution Steps
- Use a sterile syringe to draw the validated diluent volume specified by the selected vial-format table, product label or approved laboratory method.
- Inject the diluent slowly down the inside wall of the vial; avoid directing the stream onto the material and avoid foaming.
- Gently swirl or roll until fully dissolved. Do not shake.
- Label the vial with product, concentration, diluent, preparation date and operator; protect from light and refrigerate at 2–8 °C (35.6–46.4 °F) unless the product-specific method states otherwise.
- Use within the product-specific validated hold time and no later than 4 weeks after preparation unless published stability data supports a different period.
Injection Technique
Use this technique only when the product-specific approved label or authorized research protocol specifies subcutaneous administration and trained personnel are responsible for the procedure.
- Clean the vial stopper and the selected administration site with alcohol; allow both surfaces to dry completely.
- Pinch a small fold of skin and insert the needle into the subcutaneous tissue at a 45–90° angle.
- Do not aspirate during a subcutaneous injection; deliver the validated volume slowly and steadily.
- If the approved protocol specifies a volume greater than 1.0 mL, divide it between separate sites rather than using one site.
- Rotate sites systematically; commonly referenced subcutaneous sites include the abdomen, thigh and upper arm.
- Wait several seconds after delivery before withdrawing the needle to help ensure the complete validated volume is delivered.
- Discard the used syringe immediately in an approved sharps container; never recap or reuse it.
Supplies Needed
- Product vial (CJC-1295 (No DAC); use the selected labelled vial strength).
- U-100 insulin syringe (1 mL capacity) or the sterile administration device specified by the approved protocol.
- Validated diluent in the container size specified by the product label or authorized preparation method.
- Alcohol swabs and an approved sharps container—use a fresh swab for the vial stopper and each administration site.
Storage Instructions
Proper storage helps maintain product quality and stability. The supplied label, COA and product-specific validated method take precedence over these general handling rules.
- Unopened: Keep the vial sealed, dry and protected from light at the temperature stated on the supplied label; do not assume a universal shelf life.
- After preparation: Refrigerate at 2–8 °C (35.6–46.4 °F) unless the product-specific method states otherwise, and use only within its validated in-use period.
- Before opening a cold vial, allow the sealed container to equilibrate as required by the method so condensation does not enter the product.
- Long-term storage: Freeze or aliquot only when supported by product-specific stability data; avoid repeated freeze–thaw cycles and discard material with unexpected particles, discoloration or container damage.
How This Works
CJC-1295 No DAC, also called Modified GRF(1–29), is a short-acting growth-hormone-releasing hormone analogue. It binds pituitary GHRH receptors to stimulate endogenous pulsatile growth-hormone release without the albumin-binding DAC extension.
Chemical identity or a proposed mechanism does not establish an effective amount, treatment indication or safe human-use protocol.
Benefits & Side Effects
Benefits
- Growth-hormone research: CJC-1295 without DAC is used in research on transient growth-hormone and IGF-1 signaling.
- Evidence status: A sustained clinical benefit for body composition, recovery or anti-aging has not been established.
Side Effects & Evidence Limits
- Hormonal effects: Potential effects include flushing, headache, edema, tingling, appetite changes and altered glucose regulation.
- Long-term uncertainty: Safety in cancer risk, pituitary disease, diabetes and prolonged exposure is not established.
This material is provided for educational and laboratory reference only. It is not medical advice, a clinical protocol, or a recommendation for human or veterinary administration. Consult qualified professionals and applicable regulations before planning research.