10–20 days
Community course convention, not a clinical study period.

Protocol / Research Dosing Guide
An evidence-organized Cortagen guide separating AEDP preclinical work from Cortexin evidence and community protocols.
Cortagen is the synthetic tetrapeptide Ala-Glu-Asp-Pro. Its direct evidence is limited to animal and laboratory work from a narrow research base. Human studies of the different porcine extract Cortexin do not validate Cortagen.
Why researchers care
Cortical-neuron and nerve-regeneration research
Class
Synthetic AEDP tetrapeptide bioregulator
Route reported
Subcutaneous or intramuscular use is community reported
Cycle length
10–20 days reported; not validated
Regulatory status
Research-use listing; not FDA approved
The supplied source reports 0.5–2 mg once daily for 10–20 days by subcutaneous or intramuscular routes. Every value is vendor/community reported, not a clinical dose-finding result.
| Phase or study | Amount | Frequency / evidence |
|---|---|---|
| Community low | 0.5 mg daily | 10–20 days; unvalidated |
| Community common | 1 mg daily | 10–20 days; unvalidated |
| Community high | 2 mg daily | 10–20 days; unvalidated |
No validated human amount, route, frequency, course length, repeat interval, or rest period exists for synthetic Cortagen.
Neutral research-material planning only. This does not establish an appropriate amount or route.
Research planning item
Exact labeled research vial
Research planning item
Measured diluent volume
Research planning item
U-100 measurement reference
Research planning item
Alcohol swabs
Research planning item
Appropriate sharps container
Research planning item
Written concentration label
Concentration
10 mg/mL
Draw volume
0.1 mL
U-100 units
10
Mathematical draws
20
Arithmetic only. The entered amount is not a recommendation and does not establish suitability.
Community convention only.
Not established.
Not applicable to reported injection routes and not established.
No validated procedure exists.
| Route | Evidence context | Boundary |
|---|---|---|
| Subcutaneous | Community reported | No human route trial |
| Intramuscular | Community reported | Often conflated with Cortexin |
| Laboratory exposure | Cell and tissue studies | Not human dosing |
| Cortexin | Different porcine extract | Not interchangeable |
Routes and amounts are not interchangeable unless a verified study explicitly establishes a conversion.
| Measure | Finding | Evidence limit |
|---|---|---|
| Human half-life | Not established | No human PK study |
| Animal half-life | Not established | No PK study identified |
| Bioavailability | Not established | No route-specific exposure data |
| Frequency | Daily is community reported | Not trial derived |
| Route | Amount | Frequency | Source | Human validation |
|---|---|---|---|---|
| Subcutaneous | 0.5 mg | Once daily | Community report | No |
| Subcutaneous or intramuscular | 1 mg | Once daily | Community report | No |
| Subcutaneous or intramuscular | 2 mg | Once daily | Community report | No |
Published study values describe those studies. Community-reported values are not validated dosing recommendations.
Concentration: 10 mg/mL
| Entered amount | Volume | U-100 units |
|---|---|---|
| 1 mg | 0.1 mL | 10 units |
| 2 mg | 0.2 mL | 20 units |
| 3 mg | 0.3 mL | 30 units |
Reconstitution does not establish identity, purity, sterility, stability, or an appropriate amount.
Cortagen is Ala-Glu-Asp-Pro.
Current status · verified September 15, 2026
Research-use listing; not FDA approved
This is an evidence-gap and precaution list, not an approved prescribing label.
Pregnancy or breastfeeding
No safety data
Children or adolescents
No safety data
Neurologic disease needing diagnosis
No established clinical use
Known ingredient sensitivity
Potential allergic risk
Concurrent medicines
No interaction studies
Long-term or repeated use
No safety data
Important limitation: No controlled incidence.
Important limitation: No human safety dataset.
Important limitation: No immunogenicity study.
Important limitation: No controlled human assessment.
Important limitation: No interaction studies.
Important limitation: No follow-up evidence.
Community course convention, not a clinical study period.
Community reported; no restart criteria.
Not established in humans.
No validated biomarker panel or stopping rule exists.
| Claim | Evidence level | What research shows | Important limitation |
|---|---|---|---|
| Nerve regeneration | Level 2 — preclinical | Rat model | No human confirmation |
| Cortical-neuron effects | Laboratory evidence | Tissue culture | Clinical meaning unknown |
| Gene-expression regulation | Preclinical hypothesis | Limited research group | No human validation |
| Cognitive benefit | Not established | Often conflated with Cortexin | Different product |
No Cortagen-specific stability study was identified.
Community 2–8°C and 28-day guidance is not validated stability evidence.
Different formulation and handling; not transferable.
Visual inspection cannot establish purity or sterility.
Do not assign it to synthetic Cortagen.
Recheck vial mg, liquid mL, target mg, and U-100 conversion.
No controlled human Cortagen trial exists.
Do not describe the current batch as verified.
No validated procedure exists.
| Compound | Class or mechanism | Evidence | FDA status |
|---|---|---|---|
| Cortagen | Synthetic AEDP tetrapeptide | Preclinical evidence | Not approved |
| Cortexin | Porcine cortical polypeptide extract | Separate human literature | Different product |
| Cerebrolysin | Porcine peptide/amino-acid mixture | Mixed randomized evidence | Different product |
| Pinealon | Short peptide bioregulator | Limited preclinical evidence | Not approved |
The synthetic tetrapeptide Ala-Glu-Asp-Pro.
No.
No.
No controlled human Cortagen trial was identified.
Not established.
No; routes are community reported.
No.
No.
No.
It performs concentration and volume arithmetic only.
Coverage source
Community schedule and explicit Cortagen-versus-Cortexin boundary.
Open direct sourceAnimal research
Preclinical rat research; not human dosing evidence.
Open direct sourcePreclinical review
Mechanistic and preclinical context for peptide bioregulators.
Open direct source