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CategoryFat Loss
SafetyLow Risk
RegulatoryNot Evaluated
StatusResearch Only

AOD-9604

Advanced Obesity Drug 9604 · hGH Fragment 176-191

CategoryFat Loss
Half-life30–60 minutes
Routesubcutaneous, oral
RiskLow Risk
Providers182 listed#4 in Fat Loss

In brief

AOD-9604 (anti-obesity drug 9604; Tyr-hGH(177–191)) is a synthetic 16-amino-acid peptide corresponding to the C-terminal lipolytic fragment of human growth hormone, modified with an N-terminal tyrosine residue for…

Low Risk182 providers listed

About AOD-9604

AOD-9604 stimulates lipolysis and inhibits lipogenesis through mechanisms believed to be independent of the insulin-like growth factor pathway. It appears to mimic the fat-metabolising action of growth hormone without triggering the proliferative effects associated with full GH or GH-releasing peptides. Oral bioavailability has been observed in some formulations, making it of interest for non-injectable protocols.

AOD-9604 (anti-obesity drug 9604; Tyr-hGH(177–191)) is a synthetic 16-amino-acid peptide corresponding to the C-terminal lipolytic fragment of human growth hormone, modified with an N-terminal tyrosine residue for stability, and investigated as a candidate anti-obesity compound on the premise that the lipolytic activity of hGH resides in this C-terminal domain — separable from the growth-promoting and insulin-antagonizing effects mediated by other regions of the full-length molecule. AOD-9604 is proposed to stimulate fat metabolism through beta-3 adrenergic receptor-mediated pathways without activating IGF-1 production or the anabolic receptor domains of full-length GH, making it theoretically safer than GH itself for metabolic applications; preclinical studies in obese mice demonstrated lipolytic effects and body weight reduction. Clinical trials were conducted in humans by Metabolic Pharmaceuticals, and Phase 2/3 data generated in Australia suggested modest weight loss effects; however, the primary trial results were never published in PubMed-indexed peer-reviewed journals, and the best indexed primary evidence for AOD-9604 remains a preclinical study in obese mice demonstrating effects on lipid metabolism. AOD-9604 has no FDA approval and no approved indication in any jurisdiction; despite its human clinical program, the absence of published peer-reviewed primary trial data means clinical efficacy and safety cannot be independently evaluated, and the compound is currently available only as a research peptide. AOD-9604 is supplied as a lyophilized powder requiring reconstitution with bacteriostatic water before subcutaneous administration; the volume of BAC water added to the vial determines the concentration of the resulting solution, following standard peptide reconstitution methodology. Research on AOD-9604 peptide dosage was conducted in both the preclinical obese-mouse model and the Phase 2/3 human clinical program in adult obesity populations; clinical trial dosage data exists from the Metabolic Pharmaceuticals program, though primary results were not published in indexed peer-reviewed journals. Oral formulations of AOD-9604 were also evaluated in the clinical program as an alternative to subcutaneous delivery. AOD-9604 dosage context In the Metabolic Pharmaceuticals clinical program, AOD-9604 was evaluated at oral doses of 1mg and 9mg daily, and via subcutaneous injection at approximately 1mg/day in Phase 2/3 human obesity studies. In the research peptide community, subcutaneous protocols commonly reference 250–300mcg once daily, administered to the subcutaneous adipose tissue of the abdomen. These figures derive from the research context rather than an approved clinical protocol — AOD-9604 has no approved dosing for any human indication. Reconstitution follows standard peptide preparation: a 5mg vial combined with 2mL bacteriostatic water yields 2,500mcg/mL (0.1mL = 250mcg per injection). Oral formulations were evaluated in the clinical trial as a potential non-injectable route; no commercial oral AOD-9604 product exists. AOD-9604 side effects and safety profile The safety data from AOD-9604's clinical program includes several notable findings: no elevation in IGF-1 levels was observed at studied doses — a key distinction from full-length growth hormone, where IGF-1 elevation drives concerns about cell proliferation and potential oncogenicity. No significant disruption of fasting glucose or insulin sensitivity was documented. No serious adverse events attributable to AOD-9604 were reported in published trial summaries. The absence of anabolic receptor activity (no binding to the GH receptor growth-promoting domain) is the proposed basis for this benign safety profile compared to GH itself. Long-term safety data does not exist due to the absence of Phase 3 completion and product approval. Research-grade AOD-9604 carries standard purity and contamination risks associated with unregulated compounding. Providers offering AOD-9604 through supervised clinical programs are searchable in the PeptideBase provider directory.

AOD-9604 Benefits & Research Areas

selective fat tissue lipolysis via GH C-terminal fragment mechanismadipose metabolism stimulation without IGF-1 elevationoriginally developed to isolate GH lipolytic effect from growth effectssubcutaneous injection — reconstitution with bacteriostatic water required

Research Signals

Commonly researched in the context of

Calorie DeficitSedentary

Population research notes

18–2930s40s50+

These signals reflect research interest areas, not treatment indications.

Regulatory & Evidence

Risk Profile

Low Risk

Generally considered lower risk in research contexts. Risk profile varies by individual — review contraindications before use.

Regulatory Status

Availability Status
Research Only
FDA Status
Not Evaluated

HGH fragment 176-191. Drug development terminated 2007 (Phase 3 failure). FDA GRAS notice GRN 000792 for food ingredient use only — not a drug approval. No active NDA. Research chemical.

Regulatory status reflects publicly available information and may change. This is not legal or medical advice.

Research Sources

1 source cited · 1 moderate

1 Animal

  • The effect of the growth hormone fragment AOD9604 on adipose tissue

    Endocrinology · 2001

    Research in obese mouse models demonstrated that AOD9604, a C-terminal fragment of human growth hormone, stimulated lipolysis and reduced fat mass via beta-3 adrenergic receptor activation without affecting insulin-like growth factor-1 levels or blood glucose, suggesting a targeted fat-reducing mechanism.

    AnimalModeratePMID 11713213

AOD-9604 Side Effects & Safety Considerations

Low Risk

Generally considered lower risk in research contexts. Individual response varies — review all considerations before use.

Reported contraindications & considerations

Pregnant Or Nursing

Consult a qualified healthcare professional before making any health decisions. This information is educational only and does not constitute medical advice.

Research Stacks

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Where to Buy AOD-9604 — Providers & Availability

182 providers
105 Clinics6 Telehealths2 Pharmacys21 Online Vendors181 in stock1 on request

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Questions to Ask Your Provider

Frequently Asked Questions — AOD-9604

AOD-9604 (anti-obesity drug 9604; Tyr-hGH(177–191)) is a synthetic 16-amino-acid peptide corresponding to the C-terminal lipolytic fragment of human growth hormone, modified with an N-terminal tyrosine residue for stability, and investigated as a candidate anti-obesity compound on the premise that the lipolytic activity of hGH resides in this C-terminal domain — separable from the growth-promoting and insulin-antagonizing effects mediated by other regions of the full-length molecule. AOD-9604 is proposed to stimulate fat metabolism through beta-3 adrenergic receptor-mediated pathways without activating IGF-1 production or the anabolic receptor domains of full-length GH, making it theoretically safer than GH itself for metabolic applications; preclinical studies in obese mice demonstrated lipolytic effects and body weight reduction.

selective fat tissue lipolysis via GH C-terminal fragment mechanism, adipose metabolism stimulation without IGF-1 elevation, originally developed to isolate GH lipolytic effect from growth effects, subcutaneous injection — reconstitution with bacteriostatic water required.

Research on AOD-9604 primarily documents effects related to selective fat tissue lipolysis via GH C-terminal fragment mechanism and adipose metabolism stimulation without IGF-1 elevation and originally developed to isolate GH lipolytic effect from growth effects and subcutaneous injection — reconstitution with bacteriostatic water required. These are areas covered in preclinical and clinical literature — individual response varies and effects depend on context of use.

Reported contraindications and considerations for AOD-9604 include pregnant or nursing. This is educational information only — consult a qualified healthcare professional before use.

182 providers in the directory currently offer AOD-9604.

Research in obese mouse models demonstrated that AOD9604, a C-terminal fragment of human growth hormone, stimulated lipolysis and reduced fat mass via beta-3 adrenergic receptor activation without affecting insulin-like growth factor-1 levels or blood glucose, suggesting a targeted fat-reducing mechanism.

AOD-9604 is featured in the following research stacks on PeptideBase: AOD-9604 + Tirzepatide: Advanced Body Composition.

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