CJC-1295 No DAC Protocol
Shorter-acting GHRH analog variant studied for growth-hormone pulse research.
- Standard dose
- 200 mcg
- Frequency
- 1–2× daily, subcutaneous
- Route
- subcutaneous
- Cycle
- 8–12 weeks
- Vial
- 5 mg
Evidence Level: Investigational / Theoretical
Primarily preclinical or very limited human data — mechanism-based reasoning more than a demonstrated clinical effect. Treat as investigational.
Human evidence: Limited early-phase pharmacodynamic data.
Animal evidence: Preclinical GHRH-receptor studies.
Introduction & Mechanism of Action
Shorter-acting GHRH analog variant studied for growth-hormone pulse research.
GHRH(1-29) analog without the drug-affinity complex, giving it a short half-life that better mimics the body's natural pulsatile GHRH release pattern, at the cost of requiring more frequent dosing.
Receptors/targets: GHRH receptor
Areas of Research Interest
- Growth-hormone pulse research
- Recovery studies
Benefits Reported in Research
- Growth-hormone pulse research
- Recovery studies
Reported Research Dosing Range
The figures below are cited from published research literature and protocol references — they describe what has been studied, not a personal prescription or instruction.
Reported range: 100–300 mcg
Reported frequency: 1–2× daily, subcutaneous
Reported cycle duration: 8–12 weeks
Escalation & maintenance: A dedicated weekly escalation and maintenance schedule specific to this peptide has not yet been published here — follow the dose range and frequency above, titrating conservatively from the low end, and consult a physician before adjusting.
Research Reference Data
Published research on CJC-1295 No DAC reports administration at 100–300 mcg via subcutaneous route. The table below cites that published research — it is not an individualized instruction.
| Variant | Route | Reported frequency | Reported dose |
|---|---|---|---|
| Standard Protocol | subcutaneous | 1–2× daily, subcutaneous | 200 mcg |
Reconstitution Reference
Published research protocols reconstitute a 5 mg vial with 2 mL bacteriostatic water, yielding a concentration of 2.50 mg/mL. This is cited reference information, not a personalized preparation instruction — use the general research calculator below for your own reference computation.
Open the research calculator, pre-filled for CJC-1295 No DAC →Research Protocol Timeline
A reference summary of how this compound is described across published research — formulation, reported administration, and reported cycle length.
- 01
Formulation
Supplied as a lyophilized 5 mg vial requiring reconstitution before research use.
- 02
Reconstitution Reference
Published research protocols reconstitute this vial with 2 mL bacteriostatic water to reach 2.50 mg/mL.
- 03
Reported Research Administration
Published research describes 1–2× daily, subcutaneous administration via subcutaneous route, at 200 mcg per administration.
- 04
Cycle Reference
Published protocols describe a cycle duration of 8–12 weeks. Consult a physician before beginning any new research cycle.
Dilution Guide
Reconstitute with 2 mL bacteriostatic water
Bacteriostatic Water (BAC Water) is the only recommended diluent. Do not dilute with sterile water, normal saline, lidocaine, or any other solution unless explicitly specified by the manufacturer.
Handling Guide
General laboratory handling practice cited for reference — not a personalized instruction. Any human use should follow the guidance of a licensed physician.
Wash hands and clean the injection site with an alcohol swab. Pinch a fold of skin and insert the needle at a 45–90° angle for standard subcutaneous injection (abdomen, thigh, or upper arm). Inject slowly, withdraw, and apply gentle pressure. Rotate injection sites to reduce irritation, and dispose of needles in an approved sharps container.
Storage
Store lyophilized (powder) vials in a freezer at -20°C, protected from light. Once reconstituted with bacteriostatic water, refrigerate at 2–8°C and use within the timeframe recommended in your supplier documentation — typically 2–4 weeks.
Monitoring
Monitor for injection-site reactions and the side effects listed above. Stop use and consult a physician if severe or persistent reactions occur. This is a general monitoring guideline, not a personalized medical monitoring plan.
Side Effects
- Flushing
- Injection-site reaction
- Headache
Contraindications
- Active malignancy (theoretical concern)
- Pregnancy
Drug interactions
- Ghrelin-receptor agonists (e.g. Ipamorelin) — commonly combined, marketed together as CJC no-DAC / Ipamorelin
Safety
- Frequent dosing burden
- Injection-site reactions
Shorter-acting than the DAC variant, requiring more frequent dosing; human evidence remains limited.
Expected Results & Comparison
Shorter-acting than the DAC variant, requiring more frequent dosing but producing a GH-release pattern closer to natural pulsatility — this is the version most commonly paired with Ipamorelin as a combination product.
