HGH Fragment 176-191 | Per Vial
From $35.00 / vial
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The targeted fat loss peptide: isolates the lipolytic region of growth hormone to burn fat without the insulin resistance, water retention, or IGF-1 elevation of full HGH
AOD-9604 is a modified fragment of the C-terminus of human growth hormone (amino acids 176-191). It was developed by Monash University in Australia and isolated specifically for its fat-burning properties. Unlike full HGH, AOD-9604 does not bind to the GH receptor and therefore does not stimulate IGF-1 production, cause insulin resistance, or produce the hyperglycemic effects of HGH. It mimics the way natural growth hormone regulates fat metabolism: stimulating lipolysis (fat breakdown) and inhibiting lipogenesis (new fat formation), with a particularly strong effect on abdominal and visceral fat.
Also see: Full Peptides Catalog | Official info: PubMed AOD-9604 Research
AOD-9604 was designed to deliver the fat-burning benefits of growth hormone without the well-documented downsides of full HGH therapy - insulin resistance, hyperglycemia, joint pain, and IGF-1-driven tissue growth. By isolating and modifying only the C-terminal fragment (amino acids 176-191) responsible for GH's lipolytic activity, researchers created a compound with a cleaner metabolic profile. AOD-9604 does not bind to the GH receptor and does not stimulate IGF-1, making it metabolically inert outside of its direct effects on adipose tissue.
Phase I and Phase II clinical trials conducted by Metabolic Pharmaceuticals demonstrated a favorable safety profile and statistically significant reductions in body weight compared to placebo in obese subjects. The compound progressed to a Phase IIb trial before development was discontinued for commercial rather than safety reasons.
| Peptide Name | AOD-9604 (HGH Fragment 176-191) |
| Sequence | Tyr-Leu-Arg-Ile-Val-Gln-Cys-Arg-Ser-Val-Glu-Gly-Ser-Cys-Gly-Phe (cyclic) |
| Molecular Weight | 1817.1 g/mol |
| Form | Lyophilized powder for reconstitution |
| Purity | > 99% (HPLC verified) |
| Storage | Refrigerate at 2-8C; protect from light |
| Price | From $35.00 per vial |
Initial lipolytic activity begins. Users may notice mild thermogenic effect and early changes in body composition, particularly in the abdominal region.
Measurable reductions in fat mass with consistent use alongside a caloric deficit. Protocol works synergistically with resistance training and controlled nutrition.
Best results observed in 12-16 week protocols. AOD-9604 pairs well with other metabolic peptides such as CJC-1295 and Ipamorelin for comprehensive GH optimization.
AOD-9604 is administered via subcutaneous injection, typically in the abdominal region or near target fat depots. It is rapidly absorbed and distributed systemically, reaching adipose tissue within 30-60 minutes of administration.
AOD-9604 acts on adipocytes through beta-3 adrenergic receptor activation, triggering the same intracellular signaling cascade as endogenous GH's fat-metabolizing activity. This activates hormone-sensitive lipase (HSL) and promotes the release of free fatty acids from adipocytes into circulation for energy use.
Unlike many weight loss compounds that only stimulate fat breakdown, AOD-9604 simultaneously inhibits lipogenesis - the metabolic pathway responsible for converting excess calories into stored fat. This dual action creates a favorable metabolic environment for net fat mass reduction even in the absence of severe caloric restriction.
Because AOD-9604 does not bind to the GH receptor (GHR), it does not trigger the IGF-1 axis and produces no measurable effect on insulin sensitivity, blood glucose, or thyroid hormones. This makes it distinctly advantageous compared to full HGH, which at equivalent fat-loss doses would cause significant metabolic disruption and organ enlargement risk.
AOD-9604 is well-suited for adults seeking targeted fat loss - particularly visceral and abdominal fat - as part of a medically supervised body composition protocol. Its clean metabolic profile makes it appropriate for individuals who cannot use full HGH due to metabolic contraindications, and it pairs effectively with other peptides in a GH optimization stack.
Consult a licensed healthcare provider before beginning any peptide protocol. See Important Safety Information below.
AOD-9604 is a fragment of the HGH molecule (amino acids 176-191) that retains only the fat-metabolizing function of GH. Unlike full HGH, it does not bind to the GH receptor, does not elevate IGF-1, and does not affect insulin sensitivity or blood glucose. This means you get targeted fat loss without the bone/organ growth, water retention, joint pain, and metabolic disruption associated with full HGH therapy.
Most users begin to notice changes in body composition within 4-8 weeks of consistent use alongside a moderate caloric deficit. The most significant results are typically observed in 12-16 week protocols. AOD-9604 is not a rapid fat-loss agent - it works best as part of a sustained, medically supervised body recomposition protocol.
Yes. AOD-9604 is commonly used alongside GH secretagogues like CJC-1295 and Ipamorelin for comprehensive GH optimization. The combination aims to naturally elevate GH pulse amplitude (via CJC-1295/Ipamorelin) while using AOD-9604 to specifically target fat metabolism. This stack is among the most popular in anti-aging and body composition peptide protocols.
AOD-9604 is not FDA-approved as a pharmaceutical drug. It completed Phase I and Phase II clinical trials for obesity treatment in Australia and the US with favorable safety data, but development was halted for commercial reasons before Phase III. It holds FDA GRAS (Generally Recognized As Safe) status as a food ingredient (AOD9604). It is available as a research peptide for supervised wellness use.
Important Safety Information