GLP-1 & MetabolicLimited ResearchResearch Only

AOD-9604

HGH Fragment 176-191 · Stimulates lipolysis via β3-adrenergic receptor-like activation; inhibits lipogenesis (fat synthesis); mimics HGH's fat-burning C-terminal action without activating IGF-1 production or insulin-like growth effects

Not medical advice. For educational and research reference only.

Typical Dose

300 mcg daily (research protocols)

Route

Injectable

Cycle

Protocol-dependent

Storage

2–8°C Refrigerated

What is AOD-9604?

AOD-9604 is a modified C-terminal fragment (residues 176–191, Tyr-hGH177-191) of human growth hormone, studied for lipolytic and anti-obesity properties. Unlike full HGH, AOD-9604 lacks growth-promoting or diabetogenic effects but retains the fat-burning activity attributed to HGH's C-terminus. Phase IIb/III trials were conducted for obesity but fell short of the primary endpoint. Research only in the US.

Mechanism of Action

Stimulates lipolysis via β3-adrenergic receptor-like activation; inhibits lipogenesis (fat synthesis); mimics HGH's fat-burning C-terminal action without activating IGF-1 production or insulin-like growth effects

Target: β3-adrenergic receptor-like pathway

Research / educational reference. Educational research index only — not medical advice. Literature maturity is not a verdict on whether a compound works in people. Community reports are not evidence of efficacy.

Evidence at a glance

Derived · maturity-1.0

Human efficacy is unproven unless an approved label or completed published efficacy program says otherwise. Counts reflect indexed literature volume/kind — never a verdict on effect.

Literature maturity

nascent 15/100

PubMed hits

11

CT.gov trials

0

Strong-human apps

0

Sample papers

2

Sample articles by era

  • pre-20182

Application grades (curated)

  • Human-grade apps1
  • Animal / in-vitro0
  • Mechanistic0

Does literature support studied applications?

Grades reflect cited literature posture — not a treatment recommendation. Community notes are never efficacy evidence.

ApplicationCited evidenceGradeCommunity
Lipolytic fragment biology

hGH 176–191 fragment studied for fat-metabolism endpoints; not FDA-approved for weight loss.

Limited humanCommunity reports vary; not evidence of efficacy.

Pharmacology

Mechanism of action

  • •Stimulates lipolysis via β3-adrenergic receptor-like activation; inhibits lipogenesis (fat synthesis); mimics HGH's fat-burning C-terminal action without activating IGF-1 production or insulin-like growth effects
  • •Primary target framing: β3-adrenergic receptor-like pathway

Half-life

~30 minutes

Identity & chemistry

CAS
221231-10-3
Formula
C78H123N23O23S2
Molar mass
1815.1 Da
InChIKey
GVIYUKXRXPXMQM-BPXGDYAESA-N

Identity cross-checked with PubChem where available. Compass HTML used only as a bootstrap checklist — not republished as product copy.

Storage & stability

Lyophilized
2–8°C; lyophilized typical shelf 18–24 months
Reconstituted
2–8°C; in-use window often 21–30 days (product-dependent)
Tell-tale degradation
  • !Cloudiness, clumping, or particles after mixing
  • !Discoloration versus the expected clear/colorless (or labeled) solution
  • !Failed or incomplete reconstitution of lyophilized cake

Educational estimates. Prefer product labeling and peptide shelf-life tool.

Lab handling posture

Research / educational handling notes only. Not a substitute for an SDS.

  • •Use PPE appropriate for peptide powder/solution handling
  • •Avoid inhalation of lyophilized powder; handle spills per institutional policy
  • •Do not present research materials as medicines

Sample indexed literature

Research Indications

Weight LossMost Effective

Clinical trials demonstrate significant body weight reduction with sustained benefit

Blood Sugar ControlMost Effective

Improves glycemic control and A1C levels in type 2 diabetes

Cardiovascular HealthEffective

Associated with reduced cardiovascular events in high-risk patients

Metabolic SyndromeEffective

Addresses multiple components of metabolic syndrome simultaneously

Research Protocols

These are commonly discussed research protocols — not medical advice. Consult a healthcare provider before use.

GoalDoseFrequencyRoute
Starting DoseLow doseOnce weeklySubcutaneous injection
Maintenance DoseTitrated doseOnce weeklySubcutaneous injection

Peptide & Drug Interactions

Always consult your healthcare provider before combining with other compounds. Use our Interaction Checker for reference.

Other GLP-1 Agonists (e.g. Semaglutide + Tirzepatide)Avoid
InsulinMonitor
SulfonylureasMonitor
MetforminCompatible
SGLT2 InhibitorsCompatible
Oral ContraceptivesCaution
Warfarin / Blood ThinnersMonitor
NAD+Compatible

How to Reconstitute & Inject

Use bacteriostatic (BAC) water only. Avoid saline — may cause precipitation. Refrigerate and use within 28 days.

  1. 1

    Remove AOD-9604 vial from refrigeration and allow to reach room temperature (15–20 minutes)

  2. 2

    Clean vial top with alcohol swab and allow to air dry completely

  3. 3

    Using a sterile syringe, draw the calculated volume of bacteriostatic water (BAC water)

  4. 4

    Inject BAC water slowly down the side of the vial — do not aim directly at the powder

  5. 5

    Gently swirl in circular motions — DO NOT shake vigorously as this degrades the peptide

  6. 6

    Allow 2–3 minutes for full dissolution — solution should be clear and colorless

  7. 7

    Draw calculated dose into an insulin syringe for subcutaneous injection

  8. 8

    Inject into abdomen, thigh, or upper arm. Rotate injection sites to prevent lipodystrophy

  9. 9

    Store reconstituted solution refrigerated (2–8°C) and use within 28 days

What to Expect

Week 1–2

Initial appetite suppression may begin. Mild GI effects (nausea, fullness) as your body adapts.

Week 2–4

Noticeable reduction in food cravings and portion sizes. Early weight changes begin.

Week 4–8

Significant appetite control and steady weight loss. Improved blood sugar if applicable.

Week 8–16

Substantial weight reduction and enhanced energy. Metabolic markers begin improving.

Week 16–24

Major weight loss milestone with cardiovascular benefits and improved lipid profiles.

Week 24+

Maximum clinical efficacy. Comprehensive metabolic improvements and sustained benefits.

Side Effects & Safety

  • Nausea (most common, typically dose-dependent and transient)
  • Diarrhea or constipation during dose escalation
  • Vomiting, especially when starting or increasing dose
  • Reduced appetite and early satiety
  • Injection site reactions (redness, bruising)
  • Fatigue, particularly in early weeks
  • Rare: Pancreatitis — discontinue immediately with severe abdominal pain
  • Rare: Thyroid C-cell effects (contraindicated with MEN2 or thyroid cancer history)

FDA Status & Regulatory Info

Research Only

AOD-9604 is a modified C-terminal fragment (residues 176–191, Tyr-hGH177-191) of human growth hormone, studied for lipolytic and anti-obesity properties. Unlike full HGH, AOD-9604 lacks growth-promoting or diabetogenic effects but retains the fat-burning activity attributed to HGH's C-terminus. Phase IIb/III trials were conducted for obesity but fell short of the primary endpoint. Research only in the US.

Rx Required: No
503A Ban: No
Telehealth: Available
Full FDA Status Tracker

Frequently Asked Questions

Research References

External links for education only. We do not control third-party content.

Community-reported data

The information below reflects self-reported experiences from PeptIQ app users. It is not clinical evidence and should not replace professional medical advice.

Community Intelligence

What 44 users report

44 community reports

Overall experience

From check-in ratings — separate from side effects logged below. Side effects are logged separately from overall experience. A favorable check-in can still include nausea, fatigue, or injection-site reactions.

Favorable 98% · Mixed 2% · Unfavorable overall 0%

Most reported benefits

Benefits users selected when logging a favorable or mixed check-in.

Appetite
155
Recovery
155

Most logged side effects

Side effects are logged separately from overall experience. A favorable check-in can still include nausea, fatigue, or injection-site reactions.

Headache
2
Injection site irritation
1

Self-reported dose per injection

Median bucket: 0.2–0.4 mg · Most common: 0.2–0.4 mg

Reports span 0.1 to ≥ 5 mg (open-ended top bucket)

0.1–0.2 mg
4
0.2–0.4 mg
113
0.4–0.6 mg
37
5+ mg
1

Anonymized self-reports from PeptIQ users — not prescribing guidance. Buckets group similar logged amounts; open-ended top buckets mean “at least” that dose.

How repeat users are trending

Among repeat reporters, 100% said they felt similar to their last entry, 0% more positive, and 0% more negative.

Overall, repeat reporters leaned similar or mixed compared to their previous entry.

Median gap between entries: 54 days · Based on 30 repeat reporters

Share Your Experience

Rate AOD-9604 in the PeptIQ app and help the community make informed decisions.

Educational information only

This page is for educational reference. It is not medical or legal advice. PeptIQ does not sell peptides or list vendors. Consult the FDA and a licensed healthcare professional for current regulations and individualized guidance.

PeptIQ app

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Quick Facts

Half-Life
~30 minutes
Target
β3-adrenergic receptor-like pathway
Route
Injectable
Availability
Research only
Rx Required
No
503A Ban
No
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