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Growth hormone research · RESEARCH PROFILE

CJC-1295 DAC

An albumin-binding GHRH analogue studied for prolonged endocrine activity.

2 specifications·20 source documents·Source updated Jul 13, 2026

At a glance

An albumin-binding GHRH analogue studied for prolonged endocrine activity.

This profile separates the compound’s scientific background from specification-specific preparation and source schedules. Begin with the research findings and limitations, then select the formulation you want to examine.

How it works

CJC-1295 DAC engages the growth hormone-releasing hormone pathway. Its albumin-binding modification changes exposure duration, making the DAC form pharmacologically different from preparations sold without DAC.[1][2][9]

Potential benefits & side effects

Interpret each outcome in the context of the study population, formulation and evidence type. Research findings do not establish a personal treatment outcome.

Potential benefits & research findings

The cited research examines GH and IGF-1 responses. Changes in hormone measurements do not independently establish improvements in strength, recovery or longevity.[3][4][10]

Read the original publications to see the measured endpoints, comparator, duration and uncertainty. Mechanistic plausibility and a favorable experimental result are different from demonstrated clinical benefit.

Side effects & evidence limitations

Interpret the reported adverse effects together with the study population, route and observation period. Small or short studies can miss uncommon and delayed harms. Evidence from a related compound does not establish the safety of CJC-1295 DAC.

Source-reported adverse effects and cautions

  • Common side effects may include transient flushing, injection-site reactions, water retention, or headache; serious adverse effects are uncommon at standard doses[1].
  • Sources are available for independent reading. Individual claims and research schedules have not yet undergone an independent clinical review by Pep Science.

    Editorial responsibility
    Pep Science editorial desk
    Last independent review
    Not yet recorded
    Editorial standards & corrections

    SPECIFICATIONS & SOURCE SCHEDULES

    Explore a vial size

    Select the exact formulation. Vial content, target dose and prepared concentration are different measurements.

    Showing 2 mg · 1 source tables

    Source-derived research information. Table phases retain the source’s actual duration; open-ended phases are not converted into a fixed eight-week course. Review the original study before interpreting a schedule.

    Standard Weekly Approach (1 mL = 2.0 mg/mL)

    Weeks 1–12
    WeekWeekly Dose (mcg)Units (per injection) (mL)
    Weeks 1–122,000 mcg (2 mg)100 units (1.00 mL)

    Frequency: Inject once weekly subcutaneously, preferably in the evening before bed to align with natural nocturnal GH surges[5]. The peptide’s extended half-life (~6–8 days) supports weekly administration without significant loss of activity between doses[1].

    Additional schedule context & duration

    Concise summary of the once-weekly regimen.

    • Goal: Elevate endogenous GH and IGF-1 levels to support muscle growth, fat metabolism, recovery, and anti-aging research[3][4].
    • Schedule: Weekly subcutaneous injections for 8–12 weeks.
    • Dose: 2,000 mcg (2 mg) once weekly — one full vial per injection.
    • Reconstitution: 1.0 mL per 2 mg vial (2.0 mg/mL) for accurate unit measurements.
    • Storage: Lyophilized frozen; reconstituted refrigerated; avoid repeated freeze–thaw.

    Suggested weekly administration approach.

    • Standard Dose: 2,000 mcg (2 mg) once weekly[1].
    • Conservative Option: 1,000 mcg (1 mg) weekly if exploring lower doses.
    • Frequency: Once per week (subcutaneous).
    • Cycle Length: 8–12 weeks; optional 4-week break between cycles.
    • Timing: Evening administration (pre-bed) may synergize with natural nocturnal GH release; rotate injection sites weekly[5].

    Read this source protocol ↗ · View cited documents ↓

    Preparation

    Preparation and stability depend on the formulation, diluent, container and handling. The source-specific notes below apply to the selected record.
    Reconstitution Steps
    1. Draw 1.0 mL bacteriostatic water with a sterile syringe.
    2. Inject slowly down the vial wall; avoid foaming or direct stream onto the powder.
    3. Gently swirl/roll until dissolved (do not shake vigorously).
    4. Label with reconstitution date and refrigerate at 2–8 °C (35.6–46.4 °F), protected from light.

    Important: This guide is for educational purposes only and is not medical advice. For research use only. Not for human consumption.

    Storage Instructions

    Proper storage preserves peptide quality and efficacy.

    • Lyophilized: Store at −20 °C (−4 °F) in dry, dark conditions; minimize moisture exposure.
    • Reconstituted: Refrigerate at 2–8 °C (35.6–46.4 °F); use within 4 weeks and avoid freeze–thaw[6].
    • Allow vials to reach room temperature before opening to reduce condensation uptake.

    Injection Technique

    General subcutaneous guidance from clinical best-practice resources[7][8].

    • Clean the vial stopper and skin with alcohol; allow to dry completely.
    • Pinch about an inch of skin at the injection site (lower abdomen, outer thigh, or upper arm)[8].
    • Insert the needle at a 90° angle into the pinched fold (use 45° if minimal subcutaneous fat)[8].
    • Depress the plunger fully, then withdraw the needle and dispose in a sharps container.
    • Rotate sites weekly to prevent lipohypertrophy — for example, alternate between left and right abdomen[8].

    Materials & quantity planning

    Source materials checklist · 2 mg

    Plan based on an 8–12 week weekly protocol.

    • Peptide Vials (CJC-1295 DAC, 2 mg each):

      • 8 weeks: 8 vials (1 vial/week)
      • 12 weeks: 12 vials (1 vial/week)
    • Insulin Syringes (U-100, 1 mL capacity):

      • Per week: 1 syringe
      • 8 weeks: 8 syringes
      • 12 weeks: 12 syringes
    • Bacteriostatic Water (10 mL bottles): Use 1.0 mL per vial for reconstitution.

      • 8 weeks (8 vials): 8 mL1 × 10 mL bottle
      • 12 weeks (12 vials): 12 mL2 × 10 mL bottles
    • Alcohol Swabs: One for the vial stopper + one for the injection site each week.

      • Per week: 2 swabs
      • 8 weeks: 16 swabs → recommend 1 × 100-count box
      • 12 weeks: 24 swabs → recommend 1 × 100-count box

    Calculate a phased quantity

    Enter each finite phase from the schedule you are studying. Open-ended phases need an explicit duration. Calculation uses 2 mg per vial and 1 mL per vial.

    Complete each phase to calculate totals.

    Quantity estimates exclude preparation losses and expiry. Follow the formulation’s handling and disposal requirements.

    FOLLOW THE EVIDENCE

    References & further reading

    Original publications and source documents cited across this product’s variants. A listed source is not an independent endorsement of a dosing schedule.

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    Related topics are not interchangeable compounds or formulations.