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    AOD-9604 + CJC-1295 + Ipamorelin (12mg)

    SubcutaneousOnce daily12mg

    Reviewed by the AllPeptides.eu Editorial Team·Last reviewed: 2026-06-16

    🇺🇸 GRAS

    Educational information. Not medical advice, and no efficacy claim is implied. Regulatory approval is not a use recommendation by AllPeptides.eu.

    Research-only — no FDA/EMA approval
    Educational information. Not medical advice or a recommendation for use.

    ⚠️ For informational/educational purposes only. Not medical advice. We do not sell any products. Self-treatment carries serious risks — consult a healthcare professional. Disclaimer

    Free Access

    How It Works

    AOD-9604 (Anti-Obesity Drug 9604) is a modified fragment (amino acids 176-191) of human growth hormone that activates lipolysis without the anabolic or diabetogenic effects of full GH. It acts by activating β3-adrenergic receptors in adipose tissue. CJC-1295 is a modified GHRH(1-29) analog that provides prolonged GHRH signaling, increasing endogenous GH and IGF-1 for 6–8 days. Ipamorelin is a pentapeptide that binds to the ghrelin receptor (GHS-R1a), selectively stimulating GH without increasing ACTH or cortisol. The triple combination provides enhanced lipolysis, increased muscle protein synthesis, and improved body composition.

    Quick Start

    • Reconstitution: Add 3.0 mL of bacteriostatic water → 4 mg/mL total (~1.33 mg/mL per component).
    • Typical Daily Range: 100–300 mcg per component (300–900 mcg total) with gradual titration.
    • Storage: Lyophilized: freezer at −20 °C · after reconstitution: refrigerator at 2–8 °C · use within 3–4 weeks.
    Detailed Protocol Data

    12-Week Gradual Titration (3 mL = 4 mg/mL)

    Educational only
    Vial Size— affects syringe units
    BAC Water3 mL
    Concentration4.00 mg/mL

    Route: Subcutaneous | Frequency: Once daily

    WeekDoseUnits (per injection)
    Weeks 1–2
    100 mcg/component (300 mcg total)
    2.5 Units (0.03 mL)
    Weeks 3–4
    200 mcg/component (600 mcg total)
    5 Units (0.05 mL)
    Weeks 5–12
    300 mcg/component (900 mcg total)
    7.5 Units (0.07 mL)

    Studies report administration once daily subcutaneously, preferably at bedtime on an empty stomach (2+ hours after the last meal). This timing enhances nocturnal GH secretion and maximizes lipolytic action.

    Reconstitution Steps

    1. Draw up 3.0 mL of bacteriostatic water with a sterile syringe (ideally a 3 mL syringe with a 21–23 gauge needle).
    2. Inject slowly down the side of the vial; avoid foaming (do not spray directly onto the powder).
    3. Gently swirl or rotate until fully dissolved (do not shake vigorously).
    4. Note the reconstitution date and concentration (4 mg/mL); refrigerate at 2–8 °C, protected from light.

    Protocol Overview

    • Goal: Synergistic fat loss and GH enhancement via triple action: lipolysis (AOD-9604) + GHRH (CJC-1295) + GHS (Ipamorelin).
    • Schedule: Daily subcutaneous injections for 8–12 weeks, followed by a 4-week washout period.
    • Storage: Lyophilized frozen · reconstituted refrigerated · use within 3–4 weeks.

    Dosing Protocol

    • Initiation: 100 mcg per component daily (7.5 units) to assess tolerance.
    • Increase: 200 mcg per component (15 units) during weeks 3–4.
    • Target: 300 mcg per component (22.5 units) during weeks 5–12.
    • Timing: At bedtime on an empty stomach (2+ hours post-meal) for maximal GH response.
    • Cycle Duration: 8–12 weeks on, 4 weeks off.
    • Break between cycles: After the cycle, a 4–6 week washout period is recommended. The triple combination (AOD + CJC + Ipamorelin) acts on multiple pathways — the pause prevents tolerance buildup.

    Washout & Cycle Restart

    When can I restart?

    After the cycle, a 4–6 week washout period is recommended. The triple combination (AOD + CJC + Ipamorelin) acts on multiple pathways — the pause prevents tolerance buildup.

    Minimum wait period: 4 weeks

    Storage Instructions

    • Lyophilized: Store at −20 °C in dry, dark conditions.
    • Reconstituted: Refrigerate at 2–8 °C; use within 3–4 weeks.
    • Allow frozen vials to reach room temperature before opening.

    Important Notes

    • Inject on an empty stomach (2+ hours post-meal) — carbohydrate intake reduces GH response.
    • Aseptic technique: clean the vial stopper and skin with separate alcohol pads.
    Clinical Analysis & Safety

    Potential Benefits & Side Effects

    Potential Benefits:

    • Enhanced lipolysis and loss of visceral/subcutaneous fat through triple action.
    • Increased GH/IGF-1 levels without an increase in cortisol (selectivity of Ipamorelin).
    • Improved body composition — muscle mass ↑, body fat ↓.
    • Supports recovery, sleep quality, and skin elasticity.
    • Well-tolerated in clinical studies.

    Potential Side Effects:

    • Mild injection site reaction (redness, itching).
    • Transient increase in appetite due to ghrelin action (Ipamorelin/CJC).
    • Slight dizziness at high doses (rare).
    • Water retention (especially initially) — usually transient.

    ⚠️ Serious Warnings & Long-Term Risks

    The following warnings are based on published literature, FDA labels, and post-marketing surveillance. They do not constitute medical advice. Consult a healthcare professional.

    🎗️ Cancer Markers
    🟡 Moderate / Theoretical

    Theoretical risk (GH/IGF-1 elevation)

    As a GHS, increases GH. Theoretical risk for pre-existing neoplasms due to IGF-1 elevation. No clinical signal in short-term studies.

    📄 Growth Horm IGF Res 2008
    ⚠️ Other
    🟡 Moderate / Theoretical

    Failed clinical trials — questionable efficacy

    The Phase III obesity trial did not meet primary endpoint. Long-term safety as injectable has not been documented (GRAS only for oral use).

    📄 Metabolic Pharmaceuticals (Clinical Trial Data)

    References

    1. Obesity Research — AOD-9604: lipolytic action without anabolic GH effects
      View Source
    2. J Clin Endocrinol Metab — CJC-1295: prolonged increase in GH/IGF-1 for 6–8 days
      View Source
    3. Eur J Endocrinol — Ipamorelin: the first selective GH secretagogue without ACTH/cortisol effects
      View Source
    4. Endocrine Reviews — GH secretagogues: mechanisms & clinical applications
      View Source
    5. Transl Androl Urol (PMC) — GH secretagogues in improving body composition
      View Source
    Research Sources & Verified Data
    …
    Clinical Trials
    …
    PubMed Studies
    Research-only
    FDA Status
    0
    Regulatory Approvals
    Verified across ClinicalTrials.gov, PubMed & FDA

    External Sources & Regulatory Status

    Regulatory Approvals

    🇺🇸
    FDA
    GRAS

    GRAS (oral) — Not approved as an injectable

    FDA GRAS (oral only)

    No official regulatory source available yet — research peptide.

    Educational information. Not medical advice, and no efficacy claim is implied. Regulatory approval is not a use recommendation by AllPeptides.eu.

    Summary:
    1 Approvals
    0 PubMed
    0 Clinical Studies

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