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AOD-9604

Metabolic & Weight Loss

AOD-9604 is a modified peptide fragment of human growth hormone designed to stimulate fat metabolism while avoiding the adverse effects associated with hGH therapy. It promotes lipolysis, inhibits fat formation, and has a proven safety profile in human studies. It has been explored in clinical research for obesity and metabolic modulation.

Reconstitute
null mL BAC + 2mg vial
Daily Range
400–600 mcg Subcutaneous (SQ)
Once daily
Standard Dose
500 mcg
Cycle
4–8 weeks
then reassess
AOD-9604fat loss peptidelipolysisgrowth hormone fragmentmetabolic health

Dosing & Reconstitution Guide

Doses in clinical trials ranged from 250–1000 μg daily. AOD-9604 is not approved for weight loss or therapeutic use outside of regulated trials.

Standard / Gradual Approach

2mg Vialstandard
PhaseDoseVolume
Week 1300mcg
Week 2300mcg
Week 3600mcg
Week 4600mcg

Protocol Summary

Subcutaneous (SQ): Once daily · Dose range 400600 mcg with gradual titration
Oral: Once daily · Dose range 0.51.5 mg with gradual titration
Cycle Length: 4–8 weeks typical; reassess before extending

Frequency & Cycling

SubQ Injection

Inject 500 mcg in the morning while fasted. Cycle 20 days on, 10 days off, or up to 12 weeks with 2-week break. Effects build gradually; consistent use required for best outcomes.

🧪 Quick Start

Vial Size
2 mg
BAC Water
3 mL
Concentration
667 mcg/unit

Potential Benefits & Use Cases

AOD-9604 is not FDA-approved for fat loss or medical application. Research use only.
Achieves ~2.6 kg weight loss over 12 weeks at 1 mg/day vs 0.8 kg placebo in early trials (human trial)
Preferential loss of abdominal fat, resembling low-dose hGH pattern (human trial)
Does not raise IGF-1 levels; shows placebo-like safety profile with no antibody formation (human trial)
Preliminary preclinical data suggests cartilage repair and bone health potential (preclinical)
Clinical data Strong preclinical Limited data

Mechanism of Action

Stimulates lipolysis
Inhibits lipogenesis
Mimics metabolic region of hGH without affecting IGF-1 levels

Lifestyle & Optimization

timing

Inject on empty stomach, preferably before exercise.

diet

Maintain a slight caloric deficit (300–500 calories below maintenance).

exercise

Consistent resistance training and moderate cardio 4–5 times per week.

sleep

Prioritize 7–9 hours of sleep. Stay well-hydrated.

Side Effects & Safety

Long-Term Safety Data

Development terminated in 2007 — larger Phase IIb trial (536 subjects, 24 weeks) failed to achieve statistical significance; drug not FDA-approved

🧮 Dose Calculator

Concentration
10.0
mcg/unit
Draw Volume
50
units (0.500 mL)
For a 500 mcg dose, draw 50 units on a U-100 insulin syringe
🧬

Bioavailability & Absorption

SubQ Injection
High bioavailability with expected systemic absorption.
Oral Administration
Clinically relevant absorption reported for troche/sublingual forms; enhanced with mucosal delivery.
Half-Life
Approximately 4 hours
Degradation
Metabolized by proteolytic enzymes in peripheral tissue
Tissue Specificity
Primarily targets adipose tissue; also shows chondrocyte activation in cartilage
⚗️

Peptide Details

Molecular Weight
1813.1
Formula
C112H179N29O35S
Sequence
Tyr-hGH177-191
⚖️

Legal Status & Regulatory

RegionStatus
FDANot Approved
EUNot Approved
AustraliaNot Approved
CanadaNot Approved

Storage Instructions

Lyophilized (Powder)
Store lyophilized powder at 2-8°C or below
Reconstituted (Mixed)
After reconstitution, maintain at 2-8°C and use within 30 days. Protect from light and keep in original vial.