Human oral/IV studies and animal metabolic work; injectable weight-loss efficacy is not established.
What does it do?
A modified growth-hormone fragment investigated for obesity; the larger weight-loss trial did not confirm meaningful efficacy.
Approved & studied uses
Community uses Reported, unvalidated
Fat metabolism
18Lipolysis, reduced lipogenesis and metabolic-safety claims do not prove weight-loss benefit.
Joint / cartilage
18Osteoarthritis, cartilage regeneration and injury-recovery research, including hyaluronic-acid combinations.
Reasons people report using it; these do not establish benefit.18
Evidence limits
View research →The clinical benefit and long-term safety of repeated subcutaneous administration are not established by these studies.1
3 distinct primary sources or abstracts checked. Evidence may concern a parent compound, individual blend ingredient, animal, or cell model; it does not necessarily establish a benefit for this exact product.
Evidence definitions →Key safety information
All risks →Immunogenicity and impurities
FDA flags potential concerns for compounded AOD-9604.3
No FDA-approved therapeutic product identified.
Molecular information
Amino-acid sequence
- Tyr
- Leu
- Arg
- Ile
- Val
- Gln
- Cys
- Arg
- Ser
- Val
- Glu
- Gly
- Ser
- Cys
- Gly
- Phe
16 residues · N → C18
Length16 amino acids
Molecular weight · Da1815.1 Da
Formula, sequence notation & identity
Molecular formulaC78H123N23O23S24
YLRIVQCRSVEGSCGF (Tyr-Leu-Arg-Ile-Val-Gln-Cys-Arg-Ser-Val-Glu-Gly-Ser-Cys-Gly-Phe)Identity reported by Pep-Pedia; exact-product sequence and modifications have not been independently confirmed.
Modified growth-hormone C-terminal fragment with a disulfide bond.
Formula describes the peptide; counterions and formulation excipients are excluded.
Pep-Pedia identity details
17 amino acids · 1,815.1 Da
YLRIVQCRSVEGSCGF (Tyr-Leu-Arg-Ile-Val-Gln-Cys-Arg-Ser-Val-Glu-Gly-Ser-Cys-Gly-Phe)Reference description; checked chemical identity above takes precedence when available.18
Pharmacokinetics
How long does it stay in the body?
Unverified reference estimateNot independently confirmed
Reference half-life30 min17
Route / formulationSource page: Injectable. Exact PK route not verified.
Secondary-source estimate shown for this route; the population and exact formulation have not been independently matched to a human PK study. The source’s clearance label is approximately five half-lives, not zero remaining drug or a duration of effects.
50%of reference level
Illustrative scenario using an unverified reference estimate.
About 3% remaining after 2.5 h
Five half-lives in this estimated model. This is not a prediction of when effects stop.
Evidence and model details
Population: Not established by the reference estimate
Source’s stated attribution: Metabolic Pharmaceuticals trials
Source’s reported peak time: 15 min. This has not been independently confirmed and is not used in the elimination curve.
100 × 2−time / half-life. Time zero is a reference level, not the moment of administration. Absorption, repeated dosing, metabolites and clinical effects are not modeled. Five half-lives leaves 3.125%, not zero. This curve cannot determine a dosing interval.
Unverified reference estimateNot independently confirmed
Reference half-life30 min17
Route / formulationSource page: Oral. Exact PK route not verified.
Secondary-source estimate shown for this route; the population and exact formulation have not been independently matched to a human PK study. The source’s clearance label is approximately five half-lives, not zero remaining drug or a duration of effects.
50%of reference level
Illustrative scenario using an unverified reference estimate.
About 3% remaining after 2.5 h
Five half-lives in this estimated model. This is not a prediction of when effects stop.
Evidence and model details
Population: Not established by the reference estimate
Source’s stated attribution: Metabolic Pharmaceuticals trials
Source’s reported peak time: 30 min. This has not been independently confirmed and is not used in the elimination curve.
100 × 2−time / half-life. Time zero is a reference level, not the moment of administration. Absorption, repeated dosing, metabolites and clinical effects are not modeled. Five half-lives leaves 3.125%, not zero. This curve cannot determine a dosing interval.
What to expect
Study outcomes
Safety measures are not efficacy proof
The pooled oral/IV program reported no meaningful IGF-1 or glucose changes. It does not establish effective subcutaneous fat loss.1
Reported timelines
Reference & communityWeeks 1–2 / 3–4 / 5–8 / 8–12
Reference sequence: little change; subtle composition; fat loss; continued change. Negative controlled trials outweigh anecdotes.18
These are reported timelines, not a prediction of your response.
Community poll 10 topics · Pep-Pedia snapshot
Voluntary, unverified reports. These percentages do not measure effectiveness or safety.
Experience
The source hides 1 additional categories. Their labels and percentages are unavailable.
Number of responses to this question: not disclosed.
Duration of use
The source hides 5 additional categories. Their labels and percentages are unavailable.
Number of responses to this question: not disclosed.
Age range
The source hides 2 additional categories. Their labels and percentages are unavailable.
Number of responses to this question: not disclosed.
Gender
Number of responses to this question: not disclosed.
Primary goal
The source hides 4 additional categories. Their labels and percentages are unavailable.
Number of responses to this question: not disclosed.
Effectiveness
The source hides 16 additional categories. Their labels and percentages are unavailable.
Number of responses to this question: not disclosed.
Side effects
The source hides 16 additional categories. Their labels and percentages are unavailable.
Number of responses to this question: not disclosed.
Dosage frequency
The source hides 9 additional categories. Their labels and percentages are unavailable.
Number of responses to this question: not disclosed.
Would recommend
The source hides 11 additional categories. Their labels and percentages are unavailable.
Number of responses to this question: not disclosed.
How discovered
The source hides 6 additional categories. Their labels and percentages are unavailable.
Number of responses to this question: not disclosed.
Source & limitations
The source displays “1760 responses” for this profile. This is not a confirmed participant count or a denominator for individual questions.
- Voluntary self-reports from Pep-Pedia visitors; identity, treatment, outcomes and timing are unverified. These data are not efficacy or safety estimates.
- The source displays a profile-wide response label, not a confirmed unique participant count. It stays unchanged across questions. Question-specific denominators and absolute option counts are not exposed.
- Only the top five categories are displayed for some questions. Extra categories are retained as an undisplayed-category count; their labels and percentages are unavailable.
- Displayed percentages are rounded. They may not total 100%, especially where categories are hidden.
- This is a dated snapshot, not a live survey or current recommendation.
Protocols
Doses & schedules
Compare purpose, amount, route, frequency, and duration.
Source corrections
Pep-Pedia claims Australian iTRAM approval and exclusively oral trials; do not treat either as verified. FDA reviewed oral and IV studies.
Route
Scroll to compare all columns →
| Route | Dose | Frequency | Goal / evidence | Duration | References |
|---|---|---|---|---|---|
| Oral | 0.25 mg | Once daily | Safety in obesity: METAOD006Human study | 24 weeks | 1 |
Population 502 randomized adults with obesity Context Reported in a sponsor-associated pooled safety publication; this is not an injectable protocol. Source dose wording 0.25, 0.5 or 1 mg | |||||
| Oral | 0.5 mg | Once daily | Safety in obesity: METAOD006Human study | 24 weeks | 1 |
Population 502 randomized adults with obesity Context Reported in a sponsor-associated pooled safety publication; this is not an injectable protocol. Source dose wording 0.25, 0.5 or 1 mg | |||||
| Oral | 1 mg | Once daily | Safety in obesity: METAOD006Human study | 24 weeks | 1 |
Population 502 randomized adults with obesity Context Reported in a sponsor-associated pooled safety publication; this is not an injectable protocol. Source dose wording 0.25, 0.5 or 1 mg | |||||
| SubQ | 250-300 mcg | Once daily | Fat lossReference report | 8-12 weeks | 18 |
Population Population not independently verified; see the reference and linked research. Context Reported in Pep-Pedia’s educational protocol table. Study attribution and applicability to this exact product are not independently established. Pep-Pedia claims Australian iTRAM approval and exclusively oral trials; do not treat either as verified. FDA reviewed oral and IV studies. Source tabs Injectable | |||||
| SubQ | 400-500 mcg | Once daily | Enhanced fat lossReference report | 8-12 weeks | 18 |
Population Population not independently verified; see the reference and linked research. Context Reported in Pep-Pedia’s educational protocol table. Study attribution and applicability to this exact product are not independently established. Pep-Pedia claims Australian iTRAM approval and exclusively oral trials; do not treat either as verified. FDA reviewed oral and IV studies. Source tabs Injectable | |||||
| SubQ | 250 mcg | Once daily | Joint supportReference report | 8-12 weeks | 18 |
Population Population not independently verified; see the reference and linked research. Context Reported in Pep-Pedia’s educational protocol table. Study attribution and applicability to this exact product are not independently established. Pep-Pedia claims Australian iTRAM approval and exclusively oral trials; do not treat either as verified. FDA reviewed oral and IV studies. Source tabs Injectable | |||||
| SubQ | 200 mcgStarting dose | Once daily | Conservative startReference report | 8-12 weeks | 18 |
Population Population not independently verified; see the reference and linked research. Context Reported in Pep-Pedia’s educational protocol table. Study attribution and applicability to this exact product are not independently established. Pep-Pedia claims Australian iTRAM approval and exclusively oral trials; do not treat either as verified. FDA reviewed oral and IV studies. Source tabs Injectable | |||||
| Oral | 1.0 mg | Once daily | Clinical trial doseReference report | 12-24 weeks (based on trial durations) | 18 |
Population Population not independently verified; see the reference and linked research. Context Reported in Pep-Pedia’s educational protocol table. Study attribution and applicability to this exact product are not independently established. Pep-Pedia claims Australian iTRAM approval and exclusively oral trials; do not treat either as verified. FDA reviewed oral and IV studies. Source tabs Oral | |||||
No protocols match these filters.
Study and label doses retain their study context. Reference reports are unvalidated practices, not personal treatment instructions. Ranges remain ranges; escalation stages are labeled.
Reported use periods and breaks. These do not establish a safe cycle or prove that breaks prevent tolerance.
Injectable
- Use period
- 8-12 weeks
- Break
- 4 weeks between cycles
Reported timing
Morning on empty stomach, 30 min before food
Oral
- Use period
- 12-24 weeks (based on trial durations)
- Break
- Not established
Reported timing
Not specified in trials
Side effects & safety
Immunogenicity and impurities
FDA flags potential concerns for compounded AOD-9604.
3Serious-event uncertainty
FDA notes serious adverse events with unclear causal attribution.
3Route gap
Oral/IV tolerability findings do not establish repeated subcutaneous product safety.
1Safety uncertainty
Claims of excellent safety or zero reports do not establish injectable or long-term safety.
Symptoms
Persistent GI discomfort, chest tightness, severe redness/swelling, infection or allergic reactions need assessment.
Pregnancy
Pregnancy/lactation safety unstudied.
Not a complete safety screen. Discuss health decisions with a qualified clinician.
Combinations & interactions
7 entriesCheck cautions and reported pairings. A compatibility claim does not establish that a combination is safe.
Hyaluronic acid
Unverified pairingCartilage models; human benefit unestablished.18
Reference report · Pep-Pedia label: SynergisticBPC-157
Unverified pairingReported repair/weight-management pairing; untested.18
Reference report · Pep-Pedia label: CompatibleCJC-1295
Unverified pairingProposed pairing with GH stimulation; untested.18
Reference report · Pep-Pedia label: CompatibleIpamorelin
Unverified pairingDifferent proposed pathways; no combination safety established.18
Reference report · Pep-Pedia label: CompatibleSemaglutide
Unverified pairingProposed complementary weight-management mechanisms; untested.18
Reference report · Pep-Pedia label: CompatibleInsulin
Unverified pairingSource claims glucose neutrality; does not establish interaction safety.18
Reference report · Pep-Pedia label: CompatibleOther peptides or medicines
Not establishedThe cited human program does not establish safety of contemporary injectable combinations.1
Research contextNo matching interactions. Try another name or filter.
Reconstitution calculator
Enter your peptide amount and container size. Get a volume and a simple measurement scale.
Suggested final volume mL
Estimated water to add≈ mL
For dry powder, assuming negligible volume displacement. Use bacteriostatic water only if the formulation specifies it.
1 pen unit (one dial step)=
Amounts below are total blend mass. Ingredient amounts are listed separately.
| Pen units | Amount | Volume |
|---|
Ingredients per unit
Other simple scales
Convert a specific amount
Enter an amount to calculate its volume and device setting.
Calculation & assumptions
The suggestion favors a simple 1, 2, or 5 × power-of-ten amount per unit, then the largest final volume that fits. It does not choose a dose or a biologically suitable concentration.
The water estimate applies only to dry powder and assumes negligible powder displacement. Final solution volume, specified diluent, solubility, stability, sterility, cartridge compatibility, and working fill limits must be established separately. No allowance is made for priming or transfer losses.
V2 measurement specification ↗Bacteriostatic water: formulation instructions ↗Reconstitution
The human report does not establish preparation of retail subcutaneous powders.1
Study context
IV study material was reconstituted with sterile water; a transferable numeric volume is not reported.1
Reference preparation details
Reported handling information, not a validated formulation or instruction to prepare an injectable product.
Injectable
Pep-Pedia describes preparation for this route; product-specific stability has not been independently verified.
- Solvents mentioned
- Bacteriostatic water
- Reported parameters
- Source temperature: 2-8°C. · Reported post-preparation interval: 28 days.
The source describes gentle mixing and avoiding vigorous shaking.
Oral
The source describes a finished oral capsule or tablet requiring no mixing.
- Form
- Source describes a prepared product
Appearance & documentation
Appearance and a purity certificate cannot establish sterility, identity, or suitability for injection.
Reported appearanceWhite Lyophilized PowderReported appearanceClear Solution After ReconstitutionReported appearanceCertificate of AnalysisReported variationNo FDA Drug ApprovalReported variationSubQ Route Not Clinically ValidatedReported concernDiscolored or Clumped PowderReported concernWADA Prohibited
18Vial sizes
Packaging examples, not a market survey. Approved and research products are not interchangeable.
Storage after mixing
Reconstituted research vials
Pep-Pedia reports these handling limits after mixing. They are not validated stability or sterility limits for your vial.
Full storage notes from Pep-Pedia
18Lyophilized: room temp short-term, freezer long-term. Reconstituted: 2-8°C for 28 days
Room temperature
Storage depends on the formulation, diluent, container, and handling. Follow the specific product label or pharmacist’s instructions.
Pen & syringe measurements Scales, capacity & references
Pen & syringe measurements
Device units measure volume. Concentration determines the amount in mg.
1 notch = 0.01 mL
Documented 1-unit V2 models
- One dial increment
- 1 unit
- Cartridge capacity
- 3 mL
- Maximum setting
- 60 units · 0.60 mL
Use the numbered dose window. Whole-unit settings only; confirm the specification for your exact model.
1 unit = 0.01 mL
100 units = 1 mL
- 10 units
- 0.10 mL
- 30-unit capacity
- 0.30 mL
- 50 / 100-unit capacity
- 0.50 / 1 mL
Read the printed unit scale. A small line may represent 0.5, 1, or 2 units depending on the syringe.
Use the mL scale
mL syringes and calibrated pipettes
- 0.01 mL
- 10 µL
- 0.10 mL
- 100 µL
- Amount
- mL × mg/mL
Drops, sprays and other pen clicks need their own verified volume per increment. They have no universal conversion.
3 mL is cartridge capacity. It does not mean you must prepare or load 3 mL. The original vial and the pen cartridge are different containers. This reference compares measurement scales; it does not establish product or route compatibility.
Device references
AVERON V2 specifications ↗SilverLeaf V2 unit reference ↗FDA: syringe unit conversions ↗Specifications checked October 12, 2026.Research findings
Limited human dataSource context
Pep-Pedia claims Australian iTRAM approval and exclusively oral trials; do not treat either as verified. FDA reviewed oral and IV studies.
Compound identity & other names
A modified fragment of human growth hormone studied for fat metabolism. Animal findings and human oral/IV safety studies do not establish that community subcutaneous regimens cause meaningful fat loss.
Other names: AOD9604 · AOD · Anti-Obesity Drug 9604
No FDA-approved therapeutic product identified.
How it may work
Fat-metabolism effects and beta-3 adrenergic signaling were investigated preclinically; cartilage applications remain experimental.18
Human studies mostly addressed other routes
A sponsor-associated publication summarized six randomized studies, including oral treatment for up to 24 weeks and single IV exposures. It reported no clear IGF-1 or glucose-tolerance signal under those conditions.
1Early metabolic effects were in animals
A study in obese Zucker rats found reduced weight gain and greater fat breakdown. That is preclinical evidence, not proof of human weight loss.
2Source checks & newer research
AOD-9604: FDA 2024 compounding advisory briefing
FDA reviewed limited oral and IV safety information, identified possibly related chest tightness/euphoria after IV dosing, and found insufficient long-term or subcutaneous safety data. Immunogenicity and product-quality concerns remain.
FDA 2024 compounding advisory briefing; checked19Research areas and evidence gaps
Weight and fat-metabolism research. Human oral/IV studies and animal metabolic work; injectable weight-loss efficacy is not established.12
- The clinical benefit and long-term safety of repeated subcutaneous administration are not established by these studies.
- Food-ingredient safety language should not be treated as approval of an injectable drug.
Community reports Unvalidated
Pep-Pedia describes fat-loss and body-composition expectations. These are secondary claims; the retrieved human studies do not validate its injectable schedule.6
A secondary protocol description, not a clinical recommendation or a representative survey. Dose, product identity, other compounds and outcome reporting are not independently verified.
Search coverage and review status
No additional 2025–2026 peer-reviewed efficacy trial of this exact product was identified in this targeted check. Earlier evidence and unresolved listed references are retained.
- Checked
- 2026-10-12
- Search
- AOD9604 2025 2026 study site:pubmed.ncbi.nlm.nih.gov
- Catalog
- Pep-Pedia ↗ · 11 listed references retained
- Targeted search, not an exhaustive systematic review.
- Bibliography-only entries are retained for traceability and are not treated as verified findings.
- The cited 14-kDa GH fragment is a different entity; this reference does not establish AOD-9604 efficacy.
AI-prepared summaries. Independent medical editorial review is pending.
References
Original sources and review status. Open a reference to read its summary.
1Safety and tolerability of AOD9604 in humansReview status not recorded
AI-PREPARED SUMMARY
Sponsor-associated report of six randomized studies with oral or IV exposure. Its safety findings cannot validate repeated community subcutaneous use.
Human studies mostly addressed other routes
A sponsor-associated publication summarized six randomized studies, including oral treatment for up to 24 weeks and single IV exposures. It reported no clear IGF-1 or glucose-tolerance signal under those conditions.
2Metabolic studies of AOD9604 in obese ratsPrimary source checked
AI-PREPARED SUMMARY
Obese rats showed less weight gain and increased lipolysis. This does not establish a human treatment effect.
Early metabolic effects were in animals
A study in obese Zucker rats found reduced weight gain and greater fat breakdown. That is preclinical evidence, not proof of human weight loss.
Pep-Pedia bibliography · Checked 2026-10-12
3FDA: substances with potential compounding safety risksReview status not recorded
AI-PREPARED SUMMARY
FDA flags limited safety data and potential immune and impurity risks.
4PubChem: AOD-9604 chemical identityReview status not recorded
AI-PREPARED SUMMARY
Chemical record for the disulfide-containing 16-residue peptide, including formula and molecular weight.
5Safety and Tolerability of the Hexadecapeptide AOD9604 in HumansPrimary source checked
AI-PREPARED SUMMARY
Sponsor-associated report of six randomized studies with oral or IV exposure. Its safety findings cannot validate repeated community subcutaneous use.
Pep-Pedia bibliography · Checked 2026-10-12
6Pep-Pedia: aod-9604 — community referenceCommunity source checked
AI-PREPARED SUMMARY
Accessed October 12, 2026. Reports commonly discussed protocols; these schedules are unvalidated descriptions, not evidence of safety or efficacy.
7Research catalog: labeled vial examplesCatalog checked
AI-PREPARED SUMMARY
Catalog offers 5 mg and 10 mg research-vial labels. These are seller label examples, not verified contents, market-frequency estimates or supplier endorsements.
8Phase IIa / Phase IIb OPTIONS oral AOD-9604 obesity trials (linked review)Pep-Pedia report · Primary source not checked
AI-PREPARED SUMMARY
Pep-Pedia reports: Mean weight change at 1 mg/day was reported as −2.8 kg, compared with −0.8 kg on placebo at 12 weeks.
Reported population / model
300 obese adults
Reported study details
Oral 0.25, 0.5, 1.0mg/day · 12 weeks · Significant weight loss at 1mg · Additional card metadata — Phase IIb OPTIONS Trial — Oral AOD-9604 for Obesity (2006): 536 obese adults·Oral dosing·24 weeks·Failed primary endpoint
Phase IIb OPTIONS Trial — Oral AOD-9604 for Obesity (2006): The larger trial did not show significant weight-loss superiority at 12 or 24 weeks; development subsequently stopped.
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here. Multiple reference cards share this URL; their attribution may differ.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
9Effect of Intra-articular Injection of AOD9604 with or without Hyaluronic Acid in Rabbit Osteoarthritis ModelPep-Pedia report · Primary source not checked
AI-PREPARED SUMMARY
Pep-Pedia reports: The rabbit combination with hyaluronic acid had faster lameness recovery: 11±4 versus 25±2 days in controls, with better cartilage measures.
Reported population / model
Rabbits (n=32)
Reported study details
0.25mg weekly intra-articular · 4-7 weeks · Enhanced cartilage regeneration
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
10Detection and in vitro metabolism of AOD9604Pep-Pedia report · Primary source not checked
AI-PREPARED SUMMARY
Pep-Pedia reports: An assay detected 50 pg/mL and identified six candidate metabolites; CRSVEGSCG persisted longer than the parent peptide in serum.
Reported population / model
In vitro
Reported study details
Various concentrations · Metabolite identification
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
11Increase of fat oxidation and weight loss in obese mice caused by chronic treatment with human growth hormone or a modified C-terminal fragmentPep-Pedia report · Primary source not checked
AI-PREPARED SUMMARY
Pep-Pedia reports: Obese mice gained less weight and oxidized more fat; the source reports no hGH-like hyperglycemia or suppression of insulin secretion.
Reported population / model
Mice
Reported study details
Mini-osmotic pumps · 14 days · Significant weight reduction and increased fat oxidation
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
12The effects of human GH and its lipolytic fragment (AOD9604) on lipid metabolism following chronic treatment in obese mice and beta(3)-AR knock-out micePep-Pedia report · Primary source not checked
AI-PREPARED SUMMARY
Pep-Pedia reports: Chronic weight and fat effects disappeared in beta-3-receptor knockout mice, while acute energy-expenditure effects remained.
Reported population / model
Mice & Beta-3-AR knockout mice
Reported study details
14 days · Increased beta-3-AR expression, reduced adipose tissue
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
13Effects of oral administration of a synthetic fragment of human growth hormone on lipid metabolismPep-Pedia report · Primary source not checked
AI-PREPARED SUMMARY
Pep-Pedia reports: Mouse weight gain diverged after day 16, with less fat synthesis and greater fat breakdown; isolated human adipose tissue was also examined.
Reported population / model
Mice
Reported study details
Oral daily · 30 days · Reduced lipogenesis, increased lipolysis
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
14Antilipogenic action of synthetic C-terminal sequence 177-191 of human growth hormonePep-Pedia report · Primary source not checked
AI-PREPARED SUMMARY
Pep-Pedia reports: A C-terminal hGH fragment inhibited fat synthesis in laboratory assays; this does not establish a human weight-loss effect.
Reported population / model
In vitro
Reported study details
Various concentrations · Demonstrated antilipogenic activity
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
15Human Growth Hormone Fragment 176-191 Peptide Enhances the Toxicity of Doxorubicin-Loaded Chitosan Nanoparticles Against MCF-7 Breast Cancer CellsLinked reference · Not independently reviewed
REFERENCE NOTE
Listed in Pep-Pedia’s bibliography; the linked publication and its findings have not been independently verified in this pass.
Pep-Pedia bibliography · Checked 2026-10-12
16The 14-Kilodalton Human Growth Hormone Fragment a Potent Inhibitor of Angiogenesis and Tumor MetastasisThe cited 14-kDa GH fragment is a different entity; this reference does not establish AOD-9604 efficacy.Linked reference · Not independently reviewed
REFERENCE NOTE
Bibliography retained for traceability. The cited 14-kDa GH fragment is a different entity; this reference does not establish AOD-9604 efficacy.
Pep-Pedia bibliography · Checked 2026-10-12
17Pep-Pedia: AOD-9604 — reported pharmacokineticsReference estimate; not independently verified human PKCommunity source checked
AI-PREPARED SUMMARY
Lists a half-life of 30 min and a peak time of 15 min. Stated attribution: Metabolic Pharmaceuticals trials. This value is reported by a secondary reference. The stated attribution has not been independently verified as a route- and formulation-matched human PK measurement. Five half-lives is not complete clearance, and the source’s “cleared” value is not used as a measured endpoint.
Secondary reference page checked; the underlying quantitative claim is not independently confirmed. · Checked 2026-10-12
18Pep-Pedia: AOD-9604 — route-specific referenceReference page checked; underlying claims require separate verification.Community source checked
AI-PREPARED SUMMARY
Source page checked across available routes. Protocols, cycles, storage, mechanisms and pairing claims are secondary reports; checking the page does not independently validate those claims. Original concise summaries are used here.
Content coverage audit · Checked 2026-10-12
19AOD-9604: FDA 2024 compounding advisory briefingPrimary source checked
AI-PREPARED SUMMARY
FDA reviewed limited oral and IV safety information, identified possibly related chest tightness/euphoria after IV dosing, and found insufficient long-term or subcutaneous safety data. Immunogenicity and product-quality concerns remain.
AOD-9604: FDA 2024 compounding advisory briefing
FDA reviewed limited oral and IV safety information, identified possibly related chest tightness/euphoria after IV dosing, and found insufficient long-term or subcutaneous safety data. Immunogenicity and product-quality concerns remain.
Additional primary-source check · Checked 2026-10-12