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    Adipotide (10mg)

    SubcutaneousOnce daily10mg

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

    Research-only — Adipotide (clinical development halted after Phase 1)

    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

    Available sizes:
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    How It Works

    Adipotide is a peptidomimetic designed to selectively target blood vessels within white adipose tissue by binding to prohibitin-1 on the vascular endothelium. Upon binding, it delivers a pro-apoptotic sequence that triggers vessel destruction, cutting off the blood supply to adipocytes. Preclinical studies in obese rodents showed ~30% weight reduction, while obese primates experienced ~11% weight loss in 4 weeks.

    Quick Start

    • Reconstitution: Add 3.0 mL bacteriostatic water → ~3.33 mg/mL concentration.
    • Starting Dose: 250 mcg daily; titrate up by 250 mcg every 2 weeks.
    • Storage: Lyophilized: −20 °C; reconstituted: 2–8 °C; avoid freeze-thaw cycles.
    Detailed Protocol Data

    Titration Schedule (3 mL = ~3.33 mg/mL)

    Educational only
    Vial Size— affects syringe units
    BAC Water3 mL
    Concentration3.33 mg/mL

    Route: Subcutaneous | Frequency: Once daily

    WeekDoseUnits (per injection)
    Weeks 1–2
    250 mcg
    7.5 Units (0.07 mL)
    Weeks 3–4
    500 mcg
    15 Units (0.15 mL)
    Weeks 5–6
    750 mcg
    22.5 Units (0.22 mL)
    Weeks 7–8
    1000 mcg (1.0 mg)
    30 Units (0.30 mL)

    Studies report administration once daily subcutaneously. This protocol uses the most practical dilution (3.0 mL) and starts at a conservative dose with gradual titration to mitigate potential renal side effects.

    Related compounds

    Reconstitution Steps

    1. Draw 3.0 mL of bacteriostatic water with a sterile syringe.
    2. Slowly inject it down the side of the vial; avoid foaming.
    3. Gently swirl until fully dissolved (do not shake).
    4. Date and refrigerate at 2–8 °C, away from light.

    Protocol Overview

    • Goal: Targeted fat mass reduction through vascular targeting in adipose tissue.
    • Schedule: Daily subcutaneous injections for 4–8 weeks (cautious approach due to limited human data).
    • Storage: Lyophilized frozen; reconstituted refrigerated.

    Dosing Protocol

    • Start: 250 mcg daily for Weeks 1–2; increase by 250 mcg every 2 weeks.
    • Target: Up to 1000 mcg (1.0 mg) daily by Weeks 7–8 (if tolerated).
    • Frequency: Once daily (subcutaneous).
    • Cycle Duration: 4–8 weeks (extend with extreme caution).
    • Break between cycles: 8-week pause before repeating due to safety concerns.

    Washout & Cycle Restart

    When can I restart?

    8-week pause before repeating due to safety concerns.

    Minimum wait period: 8 weeks

    Storage Instructions

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

    Important Notes

    • Important: Clinical development was halted due to safety concerns (reversible nephrotoxicity at high doses). For educational purposes only.
    Clinical Analysis & Safety

    Potential Benefits & Side Effects

    Potential Benefits:

    • Targeted fat mass reduction (up to 30% in rodents, ~11% in primates)
    • Mechanism specifically targets adipose tissue vasculature
    • Data from preclinical studies only

    Potential Side Effects:

    • Clinical development was halted due to safety concerns
    • Dose-dependent, reversible nephrotoxicity in preclinical studies
    • Mild local injection site reactions (redness, swelling)
    • Long-term human safety profile: unknown

    ⚠️ 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.

    ⚠️ Other
    🟡 Moderate / Theoretical

    Adipocyte destruction — potential local risks

    Adipotide (FTPP) targets adipose tissue vasculature, causing necrosis. In primates, reversible renal tubular damage was observed. Clinical development was discontinued.

    📄 Sci Transl Med 2011
    🫘 Renal
    🔴 High Risk

    Nephrotoxicity (animal models)

    In rhesus monkeys, Adipotide caused dose-dependent kidney damage (elevated creatinine). Reversible after discontinuation, but serious concern.

    📄 Sci Transl Med 2011

    References

    1. Science Translational Medicine — Peptidomimetic targeting of white fat causes weight loss in obese primates
      View Source
    2. MD Anderson Cancer Center — Obese monkeys lose weight on drug that attacks fat's blood supply
      View Source
    3. Arrowhead Pharmaceuticals — Adipotide Phase 1 trial – first patient dosed
      View Source
    4. ScienceDaily — Obese monkeys lose weight – targeting blood vessels of fat tissue
      View Source

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    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

    Research peptide — No regulatory approval from any agency

    Research-only — Adipotide (clinical development halted after Phase 1)

    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.

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