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For research purposes onlyThese compounds aren't FDA approved. All data presented is from clinical trials for educational reference.

AOD-9604

4.8 (41)

Composition Peptide

Dosage

Quantity

1

Price

$44.99

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Made in the USA

Certificate of Analysis

Batch verified lab data

Latest

99.93%

Purity

Variant
AOD-9604 5mg
Lot #
A0112
Labeled
20mg
Actual
22.56mg
Tested
Feb 4, 2026

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Research Purposes Snapshot

AOD-9604 is a synthetic fragment of human growth hormone (hGH 176–191) engineered to engage lipolytic signaling without the full anabolic / IGF-1 axis of intact hGH. Obesity development stopped after Phase 2b, but preclinical and early clinical archives remain widely cited for metabolic and cartilage models—educational only for this listing.

β3-AR upregulation

Adipocyte reports describe marked β3-adrenergic receptor expression increases vs controls (Heffernan et al., 2001).

70%

Cartilage signal

Rabbit osteoarthritis model: ~70% cartilage thickness improvement in cited preclinical work (Kwon et al., 2015).

2.8 kg

Weight loss

OPTIONS Phase 2b narrative: ~2.8 kg mean loss at 1 mg daily over 12 weeks vs ~0.8 kg placebo (approximate).

100%

Glucose-neutral

Human trials report no meaningful fasting glucose excursions across tested doses (Stier et al., 2013).

0%

Anti-drug antibodies

Immunogenicity panels commonly report absence of neutralizing anti-AOD-9604 antibodies.

Development status

Where it stands

Phase 2b completedNot FDA-approvedWADA prohibited
Historical sponsor
Metabolic Pharmaceuticals (trial-era)
Primary indication tested
Obesity (OPTIONS program)
Phase 2b outcome
Did not meet commercial efficacy bar
Current framing
Research compound / legacy dataset
Clinical trial records — AOD-9604

Key mechanism

Why it differs from intact hGH

Full hGH elevates IGF-1, perturbs insulin sensitivity, and carries broad anabolic liability. AOD-9604 is positioned as a lipolytic-domain mimic that retains fat-oxidation biology while sparing carbohydrate metabolism and IGF-1 in human dosing ranges studied to date.

No systemic GH mimicry: trial summaries emphasize stable glucose, insulin sensitivity, IGF-1, and absent anti-peptide antibodies—contrasting classic hGH safety talking points.
  • Fat oxidation↑ similar to hGH in model systems
  • IGF-1No change
  • Blood glucoseNeutral
  • Insulin sensitivityUnchanged

What research has shown

Human obesity trials plus preclinical cartilage work

Phase 2b OPTIONS (300+ subjects)

2.8 kg

Approximate mean loss — 1 mg daily × 12 weeks

Percent weight change (illustrative)

0.25 mg2.6%
0.5 mg2.7%
1 mg2.8%
Placebo0.8%

The 24-week Phase 2b program did not achieve sponsor efficacy hurdles for obesity commercialization, yet safety and tolerability narratives remained favorable—fueling continued niche research (joint models, fat oxidation).

Key clinical observations

Human + preclinical signals

Subjects without glucose excursions (trial summaries)100%
Anti-AOD-9604 antibody formation (reported)0%
Cartilage improvement — rabbit OA model (cited)70%
Obesity indication development halted after Phase 2b; any modern use must be framed as investigational and jurisdiction-specific.
Cross-study context

AOD-9604 vs other weight-loss datapoints

  • AOD-9604 (1 mg cohorts)~2.8% BW
  • Lifestyle-only controls (trial narratives)~0.8% BW
  • Orlistat (meta-analytic comparators)~2.9% BW

Orlistat figures derive from separate meta-analyses—not a randomized head-to-head against AOD-9604.

Beyond weight loss

Other research threads

Joint repair

Cartilage-centric OA models (Kwon et al., 2015).

0 glucose Δ

Fasting glucose stable (Stier et al., 2013).

7× β3-AR

Adipocyte receptor program (Heffernan et al., 2001).

Placebo-like AE

Six-trial tolerability narrative (JOFEM-style reviews).

Joint health

Cartilage regeneration potential

Preclinical OA work describes thickness gains (~70%) with intra-articular schedules; ultrasound-guided delivery plus hyaluronic acid co-administration is discussed as synergistic in specialty case series.

  • Example regimen cited: ~0.25 mg weekly × 4–7 weeks (model-dependent)

Ann Clin Lab Sci (2015): combination ultrasound-guided IA protocols reported superior structural scores vs monotherapy arms in archived data.

Metabolism

Selective fat oxidation

Adipocyte work ties AOD-9604 to increased lipolysis / oxidation without parallel muscle catabolism or glycemic shifts in the same experimental frames.

Fat oxidation (model scale)75%
Lean mass signal0%
Glucose signal0%

Heffernan et al., 2001

Safety archive

Human exposure

600+

Patients across six clinical trials (review summaries)

No neutralizing antibodies; IGF-1 stable; carbohydrate metrics stable; AEs mirror placebo in aggregate narratives (JOFEM 2014-style collations).

Safety profile from research

Pooled trial language

Reviewed human programs describe placebo-comparable AE rates with mild injection-site complaints dominating; metabolic labs remain boringly stable versus hGH comparators.

Frequently cited mild events

15%

Injection site

Mild
8%

Headache

Mild
5%

Fatigue

Mild
3%

Nausea

Mild

No classic hGH liabilities (trial narratives)

  • Fasting glucose unchanged
  • Insulin sensitivity unchanged
  • IGF-1 unchanged
  • No anti-AOD-9604 antibody signal

Discontinuation

  • 0.25 mg<5%
  • 0.5 mg<5%
  • 1 mg<5%

Similar to placebo; few serious AEs attributed to drug; many withdrawals unrelated per CSR-style summaries.

Typical trial exclusions
Pregnancy / breastfeedingType 1 or uncontrolled T2DRecent bariatric surgeryActive malignancySevere hepatic / renal impairmentConcurrent weight-loss drugs

Storage handling reference

Peptide handling

Cold

Lyophilized: store per COA.

Reconstitution

Sterile technique; verify route.

Light

Protect from UV during prep.

Traceability

Log batch and concentration.

Researcher notes

  • 600+ unique exposures across six sponsor trials underpin the tolerability story—still not a post-market surveillance database.
  • Public reviews rarely describe tachyphylaxis, but long-term recreational use is unstudied.
  • Safety messaging holds for 24-week windows in archives; beyond that is extrapolation.
  • WADA bans the parent fragment class—assume testing positives even if labeled “research only.”

Important Research Notice

Not for human consumption. This product and all products are sold exclusively for research and educational purposes. It is not intended to diagnose, treat, cure, or prevent any disease.

All clinical trial data and research findings presented on this page are sourced from journals and official publications but should be fact checked. They are provided for educational reference only and should not be interpreted as medical advice or product claims.

By purchasing this product, you confirm that you are a qualified researcher and will use it in accordance with all applicable laws and regulations and you do not intend to use it for human consumption.