01 — Identity
What Is CJC-1295 with DAC?
Origin
Developed by ConjuChem Biotechnologies. The DAC (Drug Affinity Complex) technology uses a maleimidoproprionic acid-lysine linker that covalently binds to serum albumin after injection, dramatically extending half-life from minutes to 6–8 days.
Chemical Class
Tetrasubstituted GHRH analog with DAC modification. 30 amino acids. The albumin-binding linker is what separates this from CJC-1295 no DAC (Mod GRF 1-29).
Primary Use
Sustained GH elevation, body composition improvement, anti-aging. Weekly injection creates a persistent "GH wave" — continuous low-level GH support between natural pulses.
Administration
Subcutaneous injection. Once or twice weekly — the extended half-life makes daily injection unnecessary. Major adherence advantage over daily GHRH analogs.
DAC vs. no-DAC — key distinction: CJC-1295 with DAC creates a sustained GH "wave" — continuous low-level GH elevation that persists for nearly a week. CJC-1295 no DAC (Mod GRF 1-29) creates a sharp GH pulse that clears in 2–4 hours. These are fundamentally different pharmacokinetic profiles with different use cases. DAC = convenience and sustained elevation. No DAC = pulsatile, physiologic mimicry.
05 — Dosing Protocol
Dose Levels & Unit Draws
| Level | Dose | Syringe Draw | Description |
| LOW |
250mcg ~15 units on insulin syringe |
~15u |
Conservative weekly dose. Good for users new to GHRH analogs or those sensitive to GH-related side effects (fluid retention, joint discomfort). |
| STANDARD |
500mcg ~30 units on insulin syringe |
~30u |
Most commonly used weekly dose. Matches the lower end of published human study dosing. Best balance of efficacy and tolerability for most users. |
| HIGH |
1000mcg ~60 units on insulin syringe |
~60u |
Upper range. Used in published human studies. Monitor for GH-related side effects at this dose — fluid retention and joint discomfort are more common. Monitor glucose. |
Some users split the weekly dose into 2 injections (e.g., 500mcg × 2 = 1000mcg/week) administered on Monday and Thursday. This maintains more consistent week-to-week GH levels and may reduce side effects by avoiding a single large weekly peak. Either approach is valid.
07 — Biomarker Monitoring
Lab Tests & Optimal Ranges
▸ GH Axis Efficacy
| Biomarker | Lab Test | Clinical Range | Optimal Range |
| IGF-1 |
Serum IGF-1 |
CLINICALAge-dependent |
OPTIMALUpper third of age range |
| IGFBP-3 |
Serum IGFBP-3 |
CLINICALAge-dependent |
OPTIMALUpper third of age range |
| Fasting Glucose |
Fasting plasma glucose |
CLINICAL70–100 mg/dL |
OPTIMAL75–90 mg/dL |
| Fasting Insulin |
Serum insulin |
CLINICAL2–25 µIU/mL |
OPTIMAL2–6 µIU/mL |
| HbA1c |
Hemoglobin A1c |
CLINICAL<5.7% |
OPTIMAL4.6–5.3% |
| AST / ALT |
CMP |
CLINICALAST 10–40 / ALT 7–56 U/L |
OPTIMALAST <26 / ALT <26 U/L |
| CBC |
Complete Blood Count |
CLINICALStandard ranges |
OPTIMALMid-range |
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⚠ CJC-1295 with DAC is not FDA-approved. Human data from a 2006 publication — no subsequent large clinical trials. The sustained GH elevation created by the DAC mechanism is pharmacologically different from pulsatile GH release — long-term implications of continuous vs. pulsatile GH elevation are not fully characterized. Monitor glucose metabolism carefully. Do not use in active malignancy.