Metabolic Protocol

AOD-9604 · 5ML
AOD-9604 1.2mg/mL · 5mL

A modified fragment of human growth hormone (hGH 176-191) studied for lipolysis and body composition support, without affecting blood glucose or IGF-1 levels. Physician-reviewed. Prescription required.

GLP / Metabolic Performance Prescription Required
What It Is
AOD-9604 5ML

Mechanism of Action

AOD 9604 is a small peptide derived from the C-terminal fragment of human growth hormone (hGH). Unlike full-length GH, AOD 9604 is designed to stimulate fat metabolism without affecting blood sugar or growth of other tissues. Its primary action is on lipid metabolism pathways, rather than traditional GH–IGF-1 signaling.

AOD-9604 targets fat metabolism through direct lipolysis and inhibition of lipogenesis, without the blood-sugar or growth effects of full-length GH. Individual outcomes may differ. This protocol is not intended to diagnose, treat, cure, or prevent any disease.

AOD-9604 · 5ML
Mechanism Biological Effect
Lipolysis activation Breakdown of stored fat
Inhibition of lipogenesis Reduces fat storage
Selective GH fragment Minimal IGF-1 effects
Tissue repair (minor) Slight cartilage/ECM support
Candidate Profile

Who It's Designed For

Your physician will determine eligibility based on your complete health intake. The following profiles are commonly associated with AOD-9604 protocol candidates in clinical practice:

Fat Loss Protocol

Individuals with physician-confirmed adiposity seeking targeted metabolic support.

Insulin Sensitivity

Individuals with metabolic syndrome components seeking targeted fat-metabolism support.

Endurance & Energy

Athletes or executives seeking body-composition and metabolic efficiency support.

Combination Protocol

Patients adding AOD-9604 to a physician-reviewed metabolic stack.

Determine your candidacy

A physician will review your intake and make eligibility determination within 24–48 hours.

Outcomes & Timeline

What the Clinical Literature Indicates

All outcome language below reflects what has been observed in clinical and preclinical settings. Individual outcomes may differ significantly. These are not guarantees.

Weeks 1–4
Early-stage signaling activity may be observed. Individual outcomes may differ. Physician monitoring recommended.
Weeks 4–8
In clinical and preclinical settings, progressive effects have been associated with continued administration. Results vary by individual.
Weeks 8–12
Sustained physician-supervised administration may support continued outcomes. Your physician will evaluate protocol continuation.
Dosing Overview

Protocol Structure

Dosing is determined individually by your assigned physician. The following represents typical ranges discussed in clinical literature. Do not self-administer or adjust dosing without physician guidance.

Typical Range

300 mcg–1.2 mg/day

Administration

Subcutaneous injection

Duration

12–24 weeks (physician-determined)

Frequency

Daily to 3x weekly (physician-determined)

These ranges are indicative only. Your physician will prescribe the specific dose and schedule appropriate for your clinical profile.

What's Included

Your Protocol Package

Physician consultation — Virtual intake review and protocol consultation with your assigned NP/MD

Valid prescription — Issued by your attending physician upon protocol approval

Pharmacy-dispensed compound — Dispensed by our licensed 503A compounding pharmacy partner

Follow-up check-in — Physician review at protocol midpoint; reorder pathway established

Clinical Considerations

Contraindications & Safety Notes

Your physician will review your complete health history before determining eligibility. The following are commonly reviewed clinical considerations.

Active malignancy: Reviewed carefully in cancer history contexts. Full disclosure required.
Pregnancy or lactation: Not indicated. Contraindicated.
Diabetes medications: Disclose at intake; your physician will review glucose management.
Current medications: Disclose all medications at intake.
FAQ

Common Questions

This compound is not FDA-approved as a drug. It is dispensed as a compounded medication through licensed 503A compounding pharmacies operating under FDA guidelines. All Verum Health protocols require a valid physician prescription.
After completing your HIPAA-secure health intake, a physician or NP will review your medical history, current medications, goals, and contraindications. If you're a candidate, a virtual consultation is scheduled — typically 15–20 minutes. Turnaround is 24–48 hours from intake submission.
Protocol stacking is reviewed on a case-by-case basis during your physician consultation. Any combination protocol is evaluated for safety and clinical appropriateness. Do not combine protocols without explicit physician guidance.
Reorders are managed through your patient portal. A follow-up physician check-in is required at protocol completion before continuation is authorized. Reorder notification is sent 10 days before your protocol completes.
AOD-9604
VERUM HEALTH
From $200
Prescription required