AOD-9604
Research-Grade
AOD-9604 is a synthetic modification of the growth-hormone fragment hGH(177-191), developed in the 1990s on the hypothesis that GH's lipolytic effects are localized to its C-terminus and can be isolated from its anabolic and insulin-antagonizing activities. Preclinical animal data initially suggested AOD-9604 could mobilize fat oxidation without raising IGF-1 or impairing glucose tolerance — a potentially attractive weight-loss profile. The clinical reality has been disappointing. Metabolic Pharmaceuticals advanced AOD-9604 through several phase-2 trials in humans with obesity. The largest trial (n≈534, 2007) reported weight-loss differences versus placebo that failed to meet the pre-specified primary endpoint, and a subsequent 6-month extension did not demonstrate meaningful additional weight reduction. The sponsor discontinued obesity development and the molecule was repositioned as a cosmetic/research ingredient. Despite thin clinical evidence, AOD-9604 remains heavily marketed in off-label weight-loss peptide circles. Oral and subcutaneous protocols circulate online without trial support. More recently it has appeared in compounded cosmetic injectables, primarily in Australia.
Specifications
| Origin / Manufacturer | Synthetic |
| Regulatory Status | AU TGA: listed cosmetic ingredient |
| Active Components | AOD-9604 |
| Storage | Lyophilized room-temp; reconstituted 2–8°C |
| Form Factor | Lyophilized powder vial |
Frequently Asked Questions
Sources & References
Every clinical claim on this page traces to a primary peer-reviewed source.
- 1Heffernan M, Summers RJ, Thorburn A, et al.. The effects of human GH and its lipolytic fragment (AOD9604) on lipid metabolism following chronic treatment in obese mice and beta(3)-AR knock-out mice. Endocrinology. 2001;142(12):5182-9. doi:10.1210/endo.142.12.8522 PMID:11713213
- 2Ng FM, Sun J, Sharma L, Libinaka R, Jiang WJ, Gianello R. Metabolic studies of a synthetic lipolytic domain (AOD9401) of human growth hormone. Hormone Research. 2000;53(6):274-8. doi:10.1159/000023547 PMID:11146367
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