Reviewed & approved by Dr. Nova Reyes · Last checked 2026-10-25. ← Back to Evidence Library
Cortexin: what the evidence says
At a glance
What it is: a mix of polypeptides extracted from animal brain cortex, sold in Russia as a nervous-system drug. R6 It is usually described as coming from pig (porcine) cortex: UNVERIFIED against the Russian label.
What the evidence says: Russian randomized trials in ischemic stroke and chronic poor brain blood flow report better recovery scores. They are Russian-language, mostly small, and not repeated outside Russia; a small trial found a rival drug (Cellex) worked better. R1, R2, R3, R4
Biggest risks: in the trials, side-effect rates were described as low and similar between groups. R2, R4 Reporting is limited to abstracts. Unknown
Rating
| Human Human evidence | Limited: ischemic stroke and chronic brain ischemia, Russian RCTs R1, R2, R3, R4 · Nootropic use in healthy people: No human data |
| Animal Animal / lab evidence | Not rated here |
| Regulatory | Not FDA-approved (no Drugs@FDA record) · Russia: reported as registered in GRLS UNVERIFIED · WADA 2026: not named; S0 depends on Russian registration status UNVERIFIED |
| Established human dose | None outside Russia. Study details lists what trials used |
Evidence verdict: Human: Limited (ischemic stroke); nootropic use: No human data Card verdict: Limited (ischemic stroke) · Nootropic use: No human data Card note: Varies by use, see page
This page reports what studies used. It is not dosing advice.
Legend: HUMAN data · ANIMAL / LAB data · UNKNOWN · UNVERIFIED: not yet confirmed against a primary source
About the evidence: nearly all Cortexin trials are Russian-language and published in one Russian neurology journal. Abstracts rarely state who funded the trial. UNVERIFIED whether the manufacturer sponsored them.
What is it?
Cortexin is an animal-brain peptide extract, similar in concept to Cerebrolysin. R6 A Cochrane review covers Cerebrolysin in stroke, not Cortexin, so its conclusions do not carry over. R8
Does it work?
- Human Acute ischemic stroke, placebo-controlled: a 62-patient double-blind trial reported better recovery scores than placebo. R1 A 272-patient double-blind, placebo-controlled trial reported the best results with two courses. R2 Full numbers are not in the abstracts.
- Human IV vs intramuscular: a 490-patient double-blind trial found the two forms performed similarly (93.6% vs 86.5% with little or no disability at 90 days). There was no placebo group, so this does not show Cortexin works. R3
- Human Chronic brain ischemia: a 189-patient randomized trial reported larger benefits at the higher amount on symptoms, fatigue and sleep; effects on mood were small. R4
- Human Head-to-head: in 40 stroke patients, Cellex did better than Cortexin on stroke and memory scores. R5
- Human Other uses: Russian trials also report benefits in children's neurological conditions and in neurological complications of type 2 diabetes (110 patients, unblinded comparison). R7
- Unknown Nootropic or "brain boost" use in healthy people: no trials found.
Is it safe?
- Human In the 490-patient trial, 74 adverse events in 60 patients (IV group) vs 51 in 41 (IM group), no significant difference. R3
- Human Smaller trials describe it as well tolerated. R1, R2
- Unknown As an animal-brain extract, allergy and contamination are theoretical concerns.
Gray-market "research use only" Cortexin: extra risks
Unknown contents. Vials sold online as "research use only" are not made under drug-quality rules, so identity, strength and sterility are unknown. This is a general caution; we have not found independent testing data for this product. Unknown Vendor claims about effects in people are marketing, not evidence. Unknown
What we don't know
- Unknown Whether results repeat in trials outside Russia or in English-language peer review
- Unknown Who funded the trials
- Unknown Anything about use in healthy people
Is it legal?
Not FDA-approved (no Drugs@FDA record, openFDA query Oct 25, 2026). Russia: reported as a registered medicine in the State Register of Medicines (GRLS) UNVERIFIED, not checked against grls.rosminzdrav.ru. EU, UK, Japan, China: UNVERIFIED not checked against EMA, MHRA, PMDA or NMPA. WADA: not named on the 2026 Prohibited List; S0 bans substances with no current governmental health-authority approval, which depends on Russian registration status UNVERIFIED.
Study details
These are amounts researchers used, not recommendations.
R1 Human Human: acute ischemic stroke vs placebo (Skoromets 2008)
| Study | People / model | Route | Amount used | Follow-up | Reported | Side effects / limitations | Citation |
|---|---|---|---|---|---|---|---|
| Skoromets 2008 | 62 hemispheric ischemic stroke | Intramuscular | 20 mg/day for 10 days, started within 6 h | 28 days | Better NIHSS, Rankin, Barthel vs placebo | Small; numbers not in abstract | PMID 19431244 |
R2 Human Human: acute ischemic stroke, low amount (Aliferova 2014)
| Study | People / model | Route | Amount used | Follow-up | Reported | Side effects / limitations | Citation |
|---|---|---|---|---|---|---|---|
| Aliferova 2014 | 272 ischemic stroke | Intramuscular | 10 mg three times a day; 2 courses, 1 course + placebo, or placebo | 70 days | Best with two 10-day courses | Numbers not in abstract | PMID 24874316 |
R3 Human Human: IV vs IM equivalence (Fedin 2025)
| Study | People / model | Route | Amount used | Follow-up | Reported | Side effects / limitations | Citation |
|---|---|---|---|---|---|---|---|
| Fedin 2025 | 490 acute ischemic stroke | IV vs IM (double-dummy) | 10 mg twice a day for 10 days, then IM 10 mg twice a day for 10 days | 90 days | mRS 0–2: 93.6% vs 86.5% | No placebo arm; AEs 74/60 pts vs 51/41 pts | PMID 41524350 |
R4 Human Human: chronic cerebral ischemia (Fedin 2018)
| Study | People / model | Route | Amount used | Follow-up | Reported | Side effects / limitations | Citation |
|---|---|---|---|---|---|---|---|
| Fedin 2018 | 189 chronic brain ischemia | Intramuscular | 20 mg vs 10 mg vs basic treatment, 10 days, repeated at 6 months | ~6+ months | Dose-dependent benefit on symptoms, asthenia, sleep | Blinding not stated | PMID 30335070 |
R5 Human Human: Cellex vs Cortexin (Khabirov 2020)
| Study | People / model | Route | Amount used | Follow-up | Reported | Side effects / limitations | Citation |
|---|---|---|---|---|---|---|---|
| Khabirov 2020 | 40 early stroke recovery | IM (Cortexin) | 10 mg/day for 10 days | Not in abstract | Cellex better on NIHSS and MMSE | Small, active comparator | PMID 33449527 |
R6 Review: mechanisms (Gomazkov 2015)
R7 Human Human: type 2 diabetes neurological complications (DIACORT 2026)
| Study | People / model | Route | Amount used | Follow-up | Reported | Side effects / limitations | Citation |
|---|---|---|---|---|---|---|---|
| DIACORT 2026 | 110 T2D with neuro complications | IM | 10 mg, ten injections, added to glycine + B vitamins | 90 days | Better MoCA, HADS, neuropathy scores vs control | Blinding not stated; 5 AEs total | PMID 42133422 |
R8 Cochrane review of Cerebrolysin (not Cortexin) in stroke (2023)
Full reference list (PubMed entries checked Oct 25, 2026)
- Skoromets AA, et al. Zh Nevrol Psikhiatr Im S S Korsakova. 2008;Suppl 22:32-8. PMID 19431244
- Aliferova VM, et al. Zh Nevrol Psikhiatr Im S S Korsakova. 2014;114(4):41-6. PMID 24874316
- Fedin AI, et al. Zh Nevrol Psikhiatr Im S S Korsakova. 2025;125(12):60-7. PMID 41524350
- Fedin AI, et al. Zh Nevrol Psikhiatr Im S S Korsakova. 2018;118(9):35-42. PMID 30335070
- Khabirov FA, et al. Zh Nevrol Psikhiatr Im S S Korsakova. 2020;120(12 Vyp 2):11-5. PMID 33449527
- Gomazkov OA. Zh Nevrol Psikhiatr Im S S Korsakova. 2015. Cortexin: molecular mechanisms and targets of neuroprotective activity. PMID 26356623
- [No authors listed]. Zh Nevrol Psikhiatr Im S S Korsakova. 2026;126(4):101-12 (DIACORT). PMID 42133422
- Ziganshina LE, et al. Cochrane Database Syst Rev. 2023. Cerebrolysin for acute ischaemic stroke. PMID 37818733
Disclaimer
This page is for education and harm reduction, not medical advice or a recommendation to use Cortexin. Talk to a clinician you trust before using any drug, and report problems to FDA MedWatch (https://www.fda.gov/safety/medwatch).
Approved for Adam Greene by Dr. Nova Reyes, 2026-10-25.