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What Is AOD-9604?| Honest Peptide

What is AOD-9604? The hGH Fragment Studied for Fat Metabolism and Weight Regulation Disclaimer: Information provided is for research and educational purposes only. AOD-9604 is not approved by the FDA for therapeutic or cosmetic use. Introduction: AOD-9604 is a

Written by Peptide Therapy Guide Editorial Team
For education only

This guide cannot diagnose a condition or recommend a personal treatment plan. Discuss medical questions with a qualified professional.

What is AOD-9604?

The hGH Fragment Studied for Fat Metabolism and Weight Regulation

Disclaimer: Information provided is for research and educational purposes only. AOD-9604 is not approved by the FDA for therapeutic or cosmetic use.

Introduction:

AOD-9604 is a synthetic peptide fragment of human growth hormone (hGH 177–191) engineered to replicate hGH’s fat-metabolism effects without altering IGF-1 or glucose levels.¹ In preclinical research, it promoted lipolysis (fat breakdown) and reduced lipogenesis (fat storage) through receptor-independent mechanisms.² ³

AOD-9604 Fast Facts

Class: Synthetic hGH fragment analog (Tyr-hGH 177–191)¹

Intended purpose: Stimulate fat metabolism while avoiding hGH’s growth or glucose effects²

Mechanism: Increases fat oxidation, enhances lipolysis, suppresses lipogenesis³

Distinct from hGH: Does not activate the growth hormone receptor or raise IGF-1² ⁴

Development stage: Completed Phase II trials; discontinued after lack of clinical efficacy⁶ ⁹

Chemical Structure

AOD-9604 is a 15-amino-acid fragment of human growth hormone. It was engineered isolate hGH’s lipolytic (fat-breaking) properties without activating the growth hormone receptor or increasing IGF-1.² The design allows it to mimic hGH’s metabolic domain in a shorter, more stable form.

How AOD-9604 Works (in Brief)

AOD-9604 was engineered from the C-terminal segment of human growth hormone (amino acids 177–191) — the portion thought to influence fat metabolism.¹ ²

In preclinical models, this fragment supported fat oxidation and lipid mobilization without the broader hormonal effects of full-length hGH.³ ⁴Because it does not activate the traditional hGH receptor, its fat-metabolism effects are considered indirect and receptor-independent.²

Discovery & Research Milestones

Originally developed in the 1990s as a potential anti-obesity drug. While it showed anti-obesity signal⁶ and advanced into clinical trials, it failed to show sufficient weight-loss effects to support commercialization.⁸

Year

Study & Source

Key Finding

20002001

Heffernan MA et al¹ ² ³

AOD-9604 found to increase fat oxidation and reduce weight gain.

2000

Ng FM et al.⁴

Demonstrated metabolic benefits without hGH-induced insulin resistance.

2007

Metabolic Pharmaceuticals⁷

Reported 24-week Phase IIb results; discontinued anti-obesity program.

2013

Misra M ⁶

12-week trial showed modest signal; 24-week trial failed. Development stopped.

Stier H et al. ⁵

Summarized human safety data—well tolerated, no antibodies detected.

AOD-9604 vs HGH Fragment 176–191: What’s the Difference?

Since AOD-9604 is often described as an HGH fragment, it’s easy to confuse the two. In reality:

HGH Fragment 176–191 is the natural sequence of amino acids (176 to 191) at the C-terminal end of human growth hormone (HGH).

AOD-9604 is a modified version of this fragment, designed to enhance stability and activity in fat metabolism. ¹²

Takeaway: AOD-9604 should be thought of as an optimized, research-developed analog of HGH fragment 176–191

Feature

HGH Fragment 176–191

AOD-9604

Origin

Direct amino acid sequence from HGH

Synthetic analog of fragment 176–191

Primary Action

Stimulates lipolysis (fat breakdown)

Stimulates lipolysis + inhibits lipogenesis

Stability

Shorter half-life, limited clinical exploration

Designed to be more stable and suitable for trials

Clinical Development

Investigated mainly in preclinical studies

Entered Phase I/II obesity trials

Takeaway

AOD-9604 should be thought of as an optimized, research-developed analog of HGH fragment 176–191 — not an entirely separate peptide, but not exactly the same either. This distinction helps explain why it progressed into formal obesity trials, whereas the raw fragment itself did not.

Regulatory Status

AOD-9604 is not FDA-approved for any medical use and is listed by the FDA as a bulk drug substance that may present safety risks.⁸ Clinical development was halted after Phase IIb trials failed to meet efficacy endpoints.⁹

Summary

AOD-9604 is a synthetic analog of the HGH 177–191 fragment developed for fat-metabolism research. Preclinical studies showed lipolytic and anti-lipogenic effects, but human trials failed to demonstrate significant weight-loss outcomes. It remains available for research use only.

FAQs About AOD-9604

What is AOD-9604?

AOD-9604 is a synthetic analog of the HGH fragment 176–191, studied for fat metabolism and weight regulation.

Is AOD-9604 the same as HGH fragment 176–191?

Not exactly — AOD-9604 is a modified version of the natural fragment, designed to be more stable and active.

Does AOD-9604 build muscle like HGH?

No, it does not stimulate IGF-1 or muscle growth — its effects are limited to fat metabolism pathways.

Is AOD-9604 approved for medical use?

No, AOD-9604 is not FDA-approved and is available only for research purposes.

Connected reading

Helpful context for this guide

Source-derived material selected through this article’s indexed topics.

comparison

Comparison Table: NAD⁺, NMN, NR

Compound Structure/Source Bioavailability Conversion to NAD⁺ Research Use Typical Dosing Safety Profile Supplement Status NAD⁺ Core coenzyme, not orally stable Poor orally N/A (already NAD⁺…

Source: honestpeptide.com
Research context

Read sources and limitations before applying a claim.

3. Human Clinical Trial Results

In obese human subjects, no serious adverse events were attributed to AOD-9604.³ Side effects were generally mild and similar to placebo.

Source: honestpeptide.com ↗

Discovery & Research Milestones

The story of NAD⁺ begins over a century ago. Early biochemists noticed a mysterious “co-ferment” that made yeast ferment sugars more efficiently — a clue that energy transfer depended on a small, reusable molecule.From that simple observation grew a century of research revealing NAD⁺ as one of biology’s most indispensable molecules. Year Study & Source Key Finding Early 1900s – Discovery Harden A, Young WJ. Proc R Soc B. 1906¹ Identified an unknown “coferment” required for yeast fermentation — the first evidence of NAD⁺. 1930s – Characterization Warburg O, Christian W. Biochem Z. 1936² Defined NAD⁺ as a central electron carrier in cellular respiration and redox reactions. 1950s–1980s – Pathway Mapping Preiss J, Handler P. J Biol Chem. 1958³ Traced NAD⁺ biosynthesis from niacin and described the Preiss–Handler and salvage pathways. 2000 – Enzyme Regulation Imai S et al. Nature. 2000⁴ Linked NAD⁺ to sirtuin activation, introducing its role in gene regulation and longevity. 2004–2007 – Precursor Discovery Bieganowski P, Brenner C. Cell. 2004⁵; Tempel W et al. PLoS Biol. 2007⁶ Identified and structurally mapped the NRK pathway, showing how nicotinamide riboside and NMN boost NAD⁺. 2010–2016 – Aging & Metabolic Decline Houtkooper RH et al. Endocr Rev. 2010⁷; Camacho-Pereira J et al. Nat Med. 2016⁹ Demonstrated that NAD⁺ levels fall with age, contributing to mitochondrial dysfunction and metabolic disorders. 2018-2021 – Recent Research Braidy N et al. Antioxid Redox Signal. 2018¹¹; Yoshino M et al. Science. 2021¹² Demonstrated that NAD⁺ precursors are bioavailable and may enhance insulin sensitivity and muscle metabolism in human studies.

Source: honestpeptide.com ↗
Practical and safety references

These excerpts are educational, not personalised medical instructions.

Storage reference

Storage & Stability

Store sealed vials at –20 °C (freezer). Protect vials from moisture and light. Keep at 2–6 °C (refrigerator) and use within 4–8 weeks. Under ideal conditions, lyophilized peptides last up to 2 years. Reconstituted peptides should be used within 4-8 weeks

Source: honestpeptide.com ↗
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About the author

Peptide Therapy Guide Editorial Team

Editorial team for Peptide Therapy Guide.

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