AOD-9604
Modified fragment (amino acids 176-191) of the C-terminus of human growth hormone. Originally developed by Metabolic Pharmaceuticals as an anti-obesity agent. Failed to meet Phase 2 primary endpoints for weight loss. Repurposed as a research / supplement-market compound; in some jurisdictions classified as a food supplement.
Educational only — not medical advice. SmartPeptide does not prescribe, diagnose, or treat. Always consult a licensed healthcare provider before using any peptide, supplement, medication, or protocol.
What the research shows
AOD-9604 demonstrated lipolytic activity in animal models but FAILED to produce significant weight loss vs. placebo in human Phase 2 trials. Development as an obesity drug was discontinued. Limited preclinical evidence for cartilage repair.
What's still experimental
Any therapeutic claim. The Phase 2 failure is the strongest piece of human evidence and it was negative.
Anecdotal / community reports
Marketed by some clinics + research suppliers as a 'fat burner.' Anecdotal logs report subjective effects that are not supported by the failed Phase 2 trial.
Anecdotal reports are NOT scientific evidence. They reflect personal experience and may not generalize.
FDA approval status
Source: openFDA + DailyMed (NIH/NLM)Doses studied in research
Source: Published clinical trialWhat published trials tested or FDA-approved labels specify. Reporting research facts — not a SmartPeptide recommendation.
The doses below are aggregated from research-peptide community forums (Reddit, biohacker discussions). They are NOT supported by clinical trials, NOT FDA-approved, and NOT a SmartPeptide recommendation. Source purity, dose accuracy, and user-reported outcomes are unverifiable. We display this only because the information is publicly available elsewhere — visitors should absolutely consult a licensed clinician familiar with experimental peptides before any use.
Notes from the source: IMPORTANT: AOD-9604's Phase 2 obesity trial (Ng et al., 2007) FAILED to produce significant weight loss vs placebo. Anecdotal claims of fat-loss effects are not supported by the only relevant human-trial data.
How clinicians typically protocol this
Third-party reference · not our recommendationDosing phases, cycle lengths, and administration timing as listed in a compounding-pharmacy clinician reference guide. Shown so you can see what a real protocol looks like — and bring informed questions to a licensed clinician.
Dose numbers, frequencies, and cycle lengths in this panel are extracted from a clinician-facing reference protocol distributed by a US-based compounding pharmacy in November 2025. SmartPeptide has paraphrased all descriptive text and adds no endorsement. Always consult a licensed clinician.
Phase 2 human trials for AOD-9604 as a weight-loss drug were negative. Read the DosesStudiedPanel above for full context.
Modified fragment of human growth hormone (residues 176–191); the guide positions it for lipolysis.
Protocol phases
AM, empty stomach
8–10 weeks on / 4–8 weeks off.
Morning fasted absorption is favored in this protocol.
FDA enforcement & recalls
Live · openFDA Drug Enforcement API- Class IICompleted· Voluntary: Firm initiatedFDA record
Compounded Lyophilized AOD-9604, 3 mg For subcutaneous or intramuscular injection, Rx Only, Compounded by: Innoveix Addison, TX 75001 800-370-1910
Reason: Lack of Assurance of Sterility
Jul 9, 2021·Innoveix Pharmaceuticals Inc - Class IIOngoing· Voluntary: Firm initiatedFDA record
AOD-9604, 1200 MCG/ML, 5 ML vial The Guyer Institute of Molecular Medicine, Indianapolis, IN
Reason: Lack of Assurance of Sterility: due to concerns with production processes which cannot assure sterility of products intended to be sterile.
Nov 30, 2020·Advanced Nutriceuticals, LLC
Mechanism & targets
ChEMBL · UniProt · Open TargetsMolecule (ChEMBL)
View on ChEMBLProtein targets (UniProt)
- E3 ubiquitin-protein ligase Jade-2Q9NQC1gene: JADE2Homo sapiens· 790 aaReviewed
Scaffold subunit of some HBO1 complexes, which have a histone H4 acetyltransferase activity (PubMed:16387653). Acts as an E3 ubiquitin-protein ligase mediating the ubiquitination and subsequent proteasomal degradation of target protein histone demethylase KDM1A (PubMed:25018020). Also acts as a ubiquitin ligase E3 toward itself. Positive regulator of neurogenesis (By similarity)
- Lysine-specific histone demethylase 1AO60341gene: KDM1AHomo sapiens· 852 aaReviewed
Histone demethylase that can demethylate both 'Lys-4' (H3K4me) and 'Lys-9' (H3K9me) of histone H3, thereby acting as a coactivator or a corepressor, depending on the context (PubMed:15620353, PubMed:15811342, PubMed:16079794, PubMed:16079795, PubMed:16140033, PubMed:16223729, PubMed:27292636). Acts by oxidizing the substrate by FAD to generate the corresponding imine that is subsequently hydrolyzed (PubMed:15620353, PubMed:15811342, PubMed:16079794, PubMed:21300290, PubMed:26214369). Acts as a c…
Live research
PubMed · ClinicalTrials.gov · Europe PMC · OpenAlexEurope PMC — 388 additional records
Includes EU/UK studies and PubMed Central full-text articles. Often surfaces research weeks before PubMed indexes it.
- Peptides for Targeting Chondrogenic Induction and Cartilage Regeneration in OsteoarthritisLiao HJ, Chen HT, Chang CH., et al. · 2026Open access· cited 12×
- Safety and Efficacy of Approved and Unapproved Peptide Therapies for Musculoskeletal Injuries and Athletic PerformanceMendias CL, Awan TM. · 2026· cited 2×
- Abstracts of the 12th International Conference on Children's Bone Health· 2026Open access
- AAV Vector-Mediated Modulation of Signaling Pathways in Neurological Disorders: Insights From Cellular, Animal, and Human StudiesFarrokhi MR, Hosseini K. · 2026
Research volume (OpenAlex topic graph)
Human clinical evidence
Semantic Scholar · AI TLDRs · influence-rankedHuman-study summaries for “AOD-9604 OR (HGH AND 176-191)” are available on Semantic Scholar but the shared free-tier API quota is exhausted right now. Try refreshing in a few minutes, or check the PubMed and Europe PMC panels above for the same literature.
Research funding & verification
NIH RePORTER · CrossRef DOI registryPublication landscape
CrossRef · DOI registry- National Natural Science Foundation of China11,338 works
- National Institutes of Health1,710 works
- National Science Foundation1,586 works
- National Key Research and Development Program of China1,412 works
- Fundamental Research Funds for the Central Universities1,356 works
- Ministry of Education, Culture, Sports, Science and Technology949 works
Funder diversity is a credibility signal. Research concentrated in a single drug company's funding warrants more scrutiny than research funded across NIH, charities, and academic grants.
Preprints — cutting edge
bioRxiv · medRxiv · via Europe PMCPreprints have NOT been peer-reviewed. They are early research shared by authors before formal validation. Treat findings as preliminary.
- PreprintSafety and Efficacy of Approved and Unapproved Peptide Therapies for Musculoskeletal Injuries and Athletic PerformanceMendias CL, Awan TM. · 2026-04-07
- PreprintSafety and Efficacy of Approved and Unapproved Peptide Therapies for Musculoskeletal Injuries and Athletic PerformanceMendias CL, Awan TM. · 2025-12-12
Known risks
Generally low acute toxicity in studied populations. Hyperprolactinemia and theoretical IGF-1-axis effects are minor given lack of GH-receptor activation. Quality of research-chemical supplies varies. Long-term safety in chronic use is poorly characterized.
Reported side effects
Injection-site reactions, occasional headache. Most users tolerate well in short-term anecdotal use.
FDA adverse event reports (FAERS)
Updated quarterly by FDAWhat requires medical supervision
If considering, work with a clinician familiar with experimental peptides. Be honest about the failed Phase 2 evidence base.
Questions for your clinician
- Given AOD-9604 failed its Phase 2 obesity trial, what's the rational case for using it?
- What FDA-approved alternatives should we discuss first?
- What would change my mind about continuing?