CJC-1295 DAC Protocol: Complete Cycling & Dosing Guide
Overview
CJC-1295 DAC is a long-acting synthetic growth hormone-releasing hormone (GHRH) analogue designed to stimulate sustained endogenous growth hormone secretion. The Drug Affinity Complex (DAC) modification binds the peptide to serum albumin, creating a depot effect that extends its active half-life to 6–8 days—a dramatic increase from the minutes-long duration of native GHRH.
This extended pharmacokinetic profile makes CJC-1295 DAC fundamentally different from unmodified CJC-1295 (which requires 2–3 times weekly dosing). The once-weekly injection schedule, combined with its mechanism of stimulating endogenous GH release rather than replacing it exogenously, positions CJC-1295 DAC as a popular choice in anti-aging protocols, body composition optimization, and athletic recovery contexts.
Critical Transparency Note: CJC-1295 DAC has not been studied in humans for efficacy in muscle growth, hormonal balance, or any other therapeutic outcome. The only published human study is an analytical chemistry paper on urine metabolite detection for anti-doping purposes—it provides zero evidence of biological effect or clinical safety. The information below is based on mechanistic understanding, pharmacokinetics, and practical protocol experience in research and user communities, not clinical trial data. It is educational content only.
Standard Protocol
Dosing Framework
Standard Maintenance Dose: 1000–2000 mcg (1–2 mg) injected once weekly
- Lower end (1 mg/week): Suitable for initial users, individuals sensitive to peptides, those over 50, or those seeking conservative GH axis stimulation
- Mid-range (1.5 mg/week): The most common effective dose across protocols; balances tissue-building drive with tolerability
- Upper end (2 mg/week): Reserved for experienced users, younger athletes, or those with prior exposure to GHRH peptides
Cycle Structure
On-Cycle Duration: 12–24 weeks is standard
- 12-week cycles: Appropriate for first-time users or those testing tolerance; sufficient to assess effect trajectory
- 16-week cycles: The modal protocol; allows full tissue remodeling while minimizing desensitization risk
- 24-week cycles: Used in extended anti-aging or body composition protocols; requires monitoring for receptor tolerance
Rest Periods: 4–8 weeks between cycles
- After a 12-week cycle: 4 weeks off minimum
- After a 16-week cycle: 6 weeks off
- After a 24-week cycle: 8 weeks off
The rest period allows GH axis receptors and signaling to reset, preventing tachyphylaxis (diminishing response over time).
Dose Escalation
Most users employ a conservative titration approach:
- Week 1–2: Start at 1000 mcg once weekly; assess tolerance and response
- Week 3–4: If tolerated well, escalate to 1500 mcg once weekly
- Week 5+: Advance to 2000 mcg once weekly if further response is desired and side effects remain minimal
This approach identifies individual sensitivity before committing to higher doses and allows the body to acclimatize to GH axis upregulation.
Goal-Specific Protocols
Protocol A: Body Composition & Lipolysis (12-week cycle)
Primary Goal: Fat loss with preservation or modest lean mass gain
Dosing:
- Weeks 1–2: 1000 mcg once weekly
- Weeks 3–12: 1500 mcg once weekly
Timing: Inject on the same day each week (e.g., Monday morning)
Nutrition: Maintain a mild caloric deficit (300–500 kcal/day below maintenance); adequate protein (1.0–1.2 g/lb bodyweight)
Training: 3–4 days/week resistance training + 2–3 days/week low-intensity steady-state cardio (walking, cycling)
Rest Period: 6 weeks off before next cycle
Protocol B: Lean Mass Accumulation & Strength (16-week cycle)
Primary Goal: Muscle gain with minimal fat addition
Dosing:
- Weeks 1–2: 1000 mcg once weekly
- Weeks 3–8: 1500 mcg once weekly
- Weeks 9–16: 2000 mcg once weekly
Timing: Inject same day each week; some protocols inject in the evening to align GH pulse with sleep
Nutrition: Slight caloric surplus (200–400 kcal/day above maintenance); high protein intake (1.2–1.4 g/lb bodyweight)
Training: 4–5 days/week progressive resistance training; compound movements prioritized
Supplementation: Creatine monohydrate (5 g/day), essential amino acids or whey protein post-training
Rest Period: 6–8 weeks off
Protocol C: Recovery & Anti-Aging (20-week cycle)
Primary Goal: Tissue repair, skin quality, joint health, sustained GH signaling
Dosing:
- Weeks 1–20: 1000–1500 mcg once weekly (steady dose; no escalation)
Timing: Inject same day each week; evening injection preferred to enhance nocturnal GH secretion
Lifestyle: Emphasis on sleep (8+ hours/night), stress management, daily movement
Supplementation: Collagen peptides (10–20 g/day), hyaluronic acid, antioxidants; some add low-dose NAD+ precursors
Training: Moderate intensity; mix of resistance and mobility work
Rest Period: 8 weeks off; longer rest period to allow complete axis recovery
How to Administer: Step-by-Step
Preparation (Before Every Injection)
- Verify the Compound: Confirm the label indicates CJC-1295 DAC with a clear expiration date; all legitimate vendors provide batch/lot numbers
- Inspect the Vial: Check for particulates, discoloration, or cloudiness; a clear, colorless to slightly off-white lyophilized powder is normal
- Gather Materials: Sterile syringe (insulin or TB syringe, typically 0.5 mL), sterile needle (27 or 30 gauge), sterile bacteriostatic water or normal saline for reconstitution, alcohol swabs, sharps container
Reconstitution (First Use Only)
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Calculate Water Volume: For a standard 2 mg vial:
- Add 2 mL bacteriostatic water to achieve 1000 mcg/mL concentration
- Alternatively, add 1 mL water for 2000 mcg/mL (more concentrated, smaller injection volume)
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Draw Sterile Water: Using a fresh syringe and needle, draw the prescribed volume of bacteriostatic water
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Inject into Vial: Slowly inject the water into the CJC-1295 DAC vial at an angle; do not spray directly onto the powder
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Let Sit: Allow 2–3 minutes for the powder to fully dissolve; do not shake vigorously (can denature peptide); gentle swirling is acceptable
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Verify Clarity: The solution should be clear and colorless; if cloudiness persists, discard and obtain a fresh vial
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Label: Mark the vial with the date of reconstitution and an expiration date (typically 20–30 days if stored properly)
Weekly Injection Procedure
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Calculate Dose: Determine the volume needed based on concentration:
- If 1000 mcg/mL and dose is 1500 mcg, draw 1.5 mL
- If 2000 mcg/mL and dose is 1500 mcg, draw 0.75 mL
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Sanitize Vial Top: Swab the rubber septum of the reconstituted vial with an alcohol wipe; let dry 10 seconds
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Draw into Syringe: Using a fresh sterile needle, draw the calculated volume into the syringe; expel any air bubbles
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Select Injection Site: Typical sites are:
- Subcutaneous (preferred): Belly fat, love handles, back of upper arm, or thigh (less painful, easier administration)
- Intramuscular: Gluteus maximus, vastus lateralis, or deltoid (deeper penetration, slightly different pharmacokinetics)
- Most users prefer subcutaneous injection for convenience
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Prepare Skin: Swab the injection site with an alcohol wipe; wait 10 seconds for alcohol to dry
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Inject: Pinch or spread skin slightly; insert needle at 45–90 degrees; inject slowly to minimize pressure and discomfort; withdraw needle and apply light pressure with gauze for 5–10 seconds
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Dispose: Immediately place used needle and syringe into a sharps container; do not recap
Storage
- Unreconstituted Vial: Store at 2–8°C (refrigerator); stable for 2–3 years if unopened
- Reconstituted Solution: Store at 2–8°C; stable for 20–30 days with bacteriostatic water as diluent; do not freeze
- During Travel: Use an insulated cooler with ice packs; keep temperature between 2–8°C