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Metabolic research · RESEARCH PROFILE

AOD-9604 + CJC-1295 + Ipamorelin

A combined research record involving AOD-9604, a CJC-1295 formulation and ipamorelin.

1 specification·14 source documents·Source updated Jul 13, 2026

At a glance

A combined research record involving AOD-9604, a CJC-1295 formulation and ipamorelin.

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

This record brings together AOD-9604, a CJC-1295 formulation and ipamorelin. The scientific rationale draws on the component pathways, but a plausible combination is not proof of an additive or synergistic clinical effect. Identify the exact components, formulation and relative amounts before comparing it with a published study.[1][7][2]

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

Most component findings must be interpreted separately from evidence for the complete preparation. A co-administration study does not automatically validate a premixed vial, and a blended total is not the dose of each constituent.[1][5][2]

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 AOD-9604 + CJC-1295 + Ipamorelin.

Source-reported adverse effects and cautions

  • Mild injection-site reactions (redness, itching) with subcutaneous administration.
  • Transient flushing or warmth following injection.
  • Occasional headache or lightheadedness during initial use.
  • Sources are available for independent reading. Individual claims and research schedules have not yet undergone an independent clinical review by Pep Science.

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    Pep Science editorial desk
    Last independent review
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    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 12 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 / Gradual Approach (3 mL reconstitution)

    Week 1Week 2Weeks 3–12
    WeekDaily DoseUnits (mL)
    Week 1200 mcg AOD / 100 mcg CJC / 100 mcg Ip10 units (0.10 mL)
    Week 2300 mcg AOD / 150 mcg CJC / 150 mcg Ip15 units (0.15 mL)
    Weeks 3–12400 mcg AOD / 200 mcg CJC / 200 mcg Ip20 units (0.20 mL)

    Concentration after reconstitution: 2.0 mg/mL AOD-9604 | 1.0 mg/mL CJC-1295 | 1.0 mg/mL Ipamorelin Frequency: Inject once daily subcutaneously, preferably in the morning or before bed on an empty stomach. For ≤10‑unit (≤0.10 mL) administrations during titration, consider 30‑ or 50‑unit insulin syringes for improved readability.

    Additional schedule context & duration

    Concise summary of the once‑daily regimen.

    • Goal: Support body composition improvements through combined lipolytic and GH-stimulating mechanisms[4][5].
    • Schedule: Daily subcutaneous injections for 8–12 weeks (extend to 16 weeks if desired).
    • Dose Range: 200–400 mcg AOD / 100–200 mcg CJC / 100–200 mcg Ip daily with gradual titration.
    • Reconstitution: 3.0 mL per 12 mg vial (4 mg/mL total concentration).
    • Storage: Lyophilized frozen; reconstituted refrigerated; avoid repeated freeze–thaw.

    Suggested daily titration approach.

    • Start: 0.10 mL daily (200 mcg AOD / 100 mcg CJC / 100 mcg Ip); increase by ~0.05 mL weekly as tolerated.
    • Target: 0.20 mL daily (400 mcg AOD / 200 mcg CJC / 200 mcg Ip) by Week 3.
    • Frequency: Once per day (subcutaneous).
    • Cycle Length: 8–12 weeks; optional extension to 16 weeks.
    • Timing: Morning or before bed on an empty stomach; rotate injection sites.

    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 3.0 mL bacteriostatic water with a sterile syringe.
    2. Inject slowly down the vial wall; avoid foaming.
    3. Gently swirl/roll until dissolved (do not shake).
    4. Label and refrigerate at 2–8 °C (35.6–46.4 °F), protected from light.
    Storage Instructions

    Proper storage preserves peptide quality.

    • 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 28 days per CDC/USP guidelines[6].
    • Allow vials to reach room temperature before opening to reduce condensation uptake.

    Injection Technique

    General subcutaneous guidance from clinical best-practice resources[9].

    • Clean the vial stopper and skin with alcohol; allow to dry.
    • Pinch a skinfold; insert the needle at 45–90° into subcutaneous tissue[10][11].
    • Do not aspirate for subcutaneous injections; inject slowly and steadily[10].
    • Rotate sites systematically (abdomen, thighs, upper arms) to avoid lipohypertrophy[12].
    • Dispose of used syringes in an approved sharps container; follow local disposal regulations.

    Materials & quantity planning

    Source materials checklist · 12 mg

    Plan based on an 8–16 week daily protocol with gradual titration (maintenance dose: 0.20 mL/day).

    • Peptide Blend Vials (12 mg each):
      • 8 weeks (~11.2 mL total): 4 vials
      • 12 weeks (~16.8 mL total): 6 vials
      • 16 weeks (~22.4 mL total): 8 vials
    • Insulin Syringes (U‑100):
      • Per week: 7 syringes (1/day)
      • 8 weeks: 56 syringes
      • 12 weeks: 84 syringes
      • 16 weeks: 112 syringes
    • Bacteriostatic Water (10 mL bottles): Use 3.0 mL per vial for reconstitution.
      • 8 weeks (4 vials): 12 mL2 × 10 mL bottles
      • 12 weeks (6 vials): 18 mL2 × 10 mL bottles
      • 16 weeks (8 vials): 24 mL3 × 10 mL bottles
    • Alcohol Swabs: One for the vial stopper + one for the injection site each day.
      • Per week: 14 swabs (2/day)
      • 8 weeks: 112 swabs → recommend 2 × 100‑count boxes
      • 12 weeks: 168 swabs → recommend 2 × 100‑count boxes
      • 16 weeks: 224 swabs → recommend 3 × 100‑count boxes

    Calculate a phased quantity

    Enter each finite phase from the schedule you are studying. Open-ended phases need an explicit duration. Calculation uses 12 mg per vial and 3 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.