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    Gonadorelin (2mg)

    Subcutaneous2–3 times weekly2mg

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

    🇺🇸 FDA (Factrel®)
    🇪🇺 EMA

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

    FDA & EMA approved — for specific indications
    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

    Gonadorelin is a synthetic decapeptide identical to the endogenous gonadotropin-releasing hormone (GnRH) secreted by the hypothalamus. When administered in a short, pulsatile fashion, it binds to GnRH receptors on pituitary gonadotroph cells, triggering the release of luteinizing hormone (LH) and follicle-stimulating hormone (FSH). LH stimulates Leydig cells to produce testosterone in men and triggers ovulation in women, while FSH supports spermatogenesis and follicular development. Unlike continuous administration of GnRH agonists, which desensitizes receptors, short intermittent dosing preserves the natural pulsatile signaling pattern.

    Quick Start

    • Reconstitution: Add 2.0 mL of bacteriostatic water → 1 mg/mL (1000 mcg/mL) concentration.
    • Typical Dose Range: 50–250 mcg per injection, 2–3 times weekly.
    • Storage: Lyophilized: −20 °C; post-reconstitution, refrigerate at 2–8 °C; avoid freeze-thaw cycles.
    Detailed Protocol Data

    Typical / Maintenance Approach (2 mL = 1 mg/mL)

    Educational only
    Vial Size— affects syringe units
    BAC Water2 mL
    Concentration1.00 mg/mL

    Route: Subcutaneous | Frequency: 2–3 times weekly

    WeekDoseUnits (per injection)
    Weeks 1–2 (Initiation)
    50 mcg
    5 Units (0.05 mL)
    Weeks 3–4 (Titration)
    100 mcg
    10 Units (0.10 mL)
    Weeks 5–8 (Maintenance)
    100–150 mcg
    10–15 Units (0.10–0.15 mL)

    Studies report administration 2–3 times weekly subcutaneously on non-consecutive days (e.g., Mon/Wed/Fri).

    Related compounds

    Reconstitution Steps

    1. Withdraw 2.0 mL of bacteriostatic water.
    2. Inject slowly down the side; avoid foaming.
    3. Gently swirl/rotate until dissolved (do not shake).
    4. Note concentration (1 mg/mL) and date; refrigerate at 2–8 °C.

    Protocol Overview

    • Objective: Stimulate endogenous LH and FSH release to support testosterone production and testicular function.
    • Schedule: Subcutaneous injections 2–3 times weekly for 4–8 weeks; off-periods.
    • Storage: Lyophilized frozen; reconstituted refrigerated; avoid freeze-thaw cycles.

    Dosing Protocol

    • Initiation: 50–100 mcg per injection; assess tolerance before increasing.
    • Target: 100–150 mcg per injection, 2–3 times weekly.
    • Frequency: Non-consecutive days (e.g., Mon/Wed/Fri) to mimic pulsatile GnRH release.
    • Cycle Duration: 4–8 weeks; off-periods to maintain pituitary sensitivity.
    • Timing: Morning administration preferred; rotate sites.
    • Break between cycles: Following the cycle (4–8 weeks), a 4–6 week washout period is recommended. The break maintains GnRH receptor sensitivity.

    Washout & Cycle Restart

    When can I restart?

    Following the cycle (4–8 weeks), a 4–6 week washout period is recommended. The break maintains GnRH receptor sensitivity.

    Minimum wait period: 4 weeks

    Storage Instructions

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

    Important Notes

    • Limit continuous daily dosing to ≤14 days to avoid receptor desensitization.
    Clinical Analysis & Safety

    Potential Benefits & Side Effects

    Potential Benefits:

    • Supports endogenous testosterone production via LH stimulation.
    • May help maintain testicular volume and function during exogenous testosterone therapy.
    • Promotes spermatogenesis and fertility in hypogonadotropic hypogonadism with pulsatile regimens.
    • Generally well-tolerated; occasional mild injection site reactions.
    • Potential for transient headache or flushing shortly after injection.

    Potential Side Effects:

    • Occasional mild injection site reactions (redness, itching, swelling).
    • Potential for transient headache or flushing.

    ⚠️ 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.

    🧬 Endocrine
    🟡 Moderate / Theoretical

    Hypogonadism with chronic use (downregulation)

    Continuous (non-pulsatile) GnRH administration leads to receptor downregulation → iatrogenic hypogonadism. Therapeutically used as 'chemical castration' in prostate cancer.

    📄 NEJM 1986

    References

    1. GnRH Agonists: Gonadorelin, Leuprolide, Nafarelin — Pharmacology and Clinical Applications — GnRH agonists: gonadorelin, leuprolide, and nafarelin – pharmacology and clinical applications
      View Source
    2. Gonadorelin Injection: Routes and Indications — Mayo Clinic — Gonadorelin injection: routes of administration and indications
      View Source
    3. GnRH Analogues: Pulsatile vs. Continuous Effects on FSH/LH (PMC) — GnRH analogues: pulsatile vs. continuous effects on FSH/LH
      View Source
    4. Gonadotropin Therapy in Hypogonadotropic Hypogonadism — Spermatogenesis and Fertility — Gonadotropin therapy in hypogonadotropic hypogonadism – spermatogenesis and fertility
      View Source
    5. Pulsatile Gonadorelin Pump Induces Spermatogenesis in Congenital HH (PMC) — Pulsatile gonadorelin pump induces spermatogenesis in congenital HH
      View Source

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    Research Sources & Verified Data
    …
    Clinical Trials
    …
    PubMed Studies
    Approved
    FDA Status
    2
    Regulatory Approvals
    Verified across ClinicalTrials.gov, PubMed & FDA

    External Sources & Regulatory Status

    Regulatory Approvals

    🇺🇸
    FDA
    Approved

    Factrel® · LH/FSH diagnostic (1973)

    🇪🇺
    EMA
    Approved

    Diagnostic / Infertility

    FDA + EMA approved

    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:
    2 Approvals
    0 PubMed
    0 Clinical Studies

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