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Compounds › Verified against primary sources

Neuro and cognition — the Russian bloc and what has a label

Noopept, phenylpiracetam, bromantane, and cortexin together have 0 registered studies on ClinicalTrials.gov; lecanemab and donanemab already have active registration

Partially approvedVerified against primary sources

Experimental material. Read before using anything from here.

Nothing on this page is a medical recommendation, prescription or treatment plan. It is an organized translation of protocols circulating in research communities and, where it exists, of what published trials tested. The two are marked differently — and they are not equivalent.

Most of the compounds here have no FDA approval for human use. Several are sold labeled "research use only", which means they have not gone through purity, sterility or dosage controls for human consumption. A community-reported dose is not a validated dose: it is what someone reported having done.

Talk to a licensed health professional before considering any of these compounds. If you already use one and feel anything unexpected, seek care — do not wait for the next routine test.

Specific note on this compound: This site already has a nootropics page and one on Eastern European medications, and their central finding still holds: literature published within a single research system, with little replication outside it, isn't the same thing as absent evidence — but it isn't confirmed evidence either. The anti-amyloids are here as a contrast of scale, not as a suggestion: they are hospital infusions with imaging monitoring, and their risk profile has no parallel with anything sold in a bottle.

Summary

Thirteen lines split into two halves that don't look alike. On one side, the nootropics from the East — noopept, phenylpiracetam, bromantane, cortexin — and the experimental dihexa and P021. On the other, the ones with a package insert: modafinil, esketamine, zuranolone, KarXT, and the two anti-amyloids lecanemab and donanemab. The split shows up in a single column. The four from the Russian bloc total 0 registered studies on ClinicalTrials.gov, despite totaling 435 articles on PubMed. Already, lecanemab and donanemab have active registration — LEQEMBI and KISUNLA — in the nervous system and anti-dementia classes.

Two halves the conversation usually lumps together

The conversation about cognition lumps together, on the same list, a Russian powder bought online and a monoclonal antibody approved by an agency. The table below measures both with the same ruler — number of articles, number of registered studies, number of phase 3 trials — and the ruler does the separating on its own.

Four methodological caveats, written before the numbers. One: the KarXT search uses xanomeline AND trospium, the two active ingredients, because that's how the registration is written. Two: "P021" in quotes returns articles that use the code for other things — the number is a ceiling. Three: the only phase 3 registration for XPro1595 that the search returns is for COVID-19, not Alzheimer's. Four: esketamine appears under the spelling ESCETAMINA, which is the one the database uses.

No number on this page came from the site's secondary source.

How much evidence exists, compound by compound

The numbers below were compiled by me on September 12, 2026, on PubMed and ClinicalTrials.gov. Each row's query is written out in full, next to the number, so anyone can repeat it and contradict me — and so the script that rechecks this site's counts can run all of them.

The condition column is not a claim about mechanism: it's the Condition field copied from the phase 3 records that the search itself returned. When there is no phase 3 record, the cell says so.

CompoundCondition in phase 3 registrationsQueryArticles in PubMedStudies on ClinicalTrials.gov
Noopeptno phase 3 registration in this searchnoopept OR "GVS-111"1130
Phenylpiracetamno phase 3 registration in this searchphenylpiracetam OR fonturacetam310
Bromantaneno phase 3 registration in this searchbromantane OR ladasten740
Cortexinno phase 3 registration in this searchcortexin2170
Dihexano phase 3 registration in this searchdihexa180
P021no phase 3 registration in this search"P021"450
ModafinilCocaine Addiction; Cocaine Dependence; Narcolepsy; Attention Deficit Hyperactivity Disordermodafinil2.412216
LecanemabAlzheimer's Disease; Preclinical Alzheimer's Disease; Early Preclinical Alzheimer's Disease; Early Alzheimer's Diseaselecanemab91934
DonanemabMild Cognitive Impairment (MCI); Alzheimer Disease; Dementia; Plaquedonanemab46419
KarXTSchizophreniaxanomeline AND trospium15945
ZuranoloneMajor Depressive Disorder; Depressive Disorder; Major; Insomniazuranolone19017
EsketamineTreatment Resistant Depression; Major Depressive Disorder; Depressive Disorder; Majoresketamine2.420353
XPro1595COVID-19XPro1595755

What exists in phase 3, and who it belongs to

Article count measures academic attention, not outcome evidence. The table below separates what has a registered phase 3 trial — and shows the largest registration the search returned in each row, with the declared number of participants and the sponsor.

A registration is not a result. A recruiting phase 3 trial is declared intent with money behind it, and nothing more than that.

CompoundQueryRegistered phase 3 trialsThe largest registration I opened
Noopept(noopept OR "GVS-111") AND AREA[Phase]PHASE30
Phenylpiracetam(phenylpiracetam OR fonturacetam) AND AREA[Phase]PHASE30
Bromantane(bromantane OR ladasten) AND AREA[Phase]PHASE30
Cortexin(cortexin) AND AREA[Phase]PHASE30
Dihexa(dihexa) AND AREA[Phase]PHASE30
P021("P021") AND AREA[Phase]PHASE30
Modafinil(modafinil) AND AREA[Phase]PHASE352NCT00343811 · n = 120 · Cephalon
Attention Deficit Hyperactivity Disorder
Lecanemab(lecanemab) AND AREA[Phase]PHASE36NCT03887455 · n = 1,906 · Eisai Inc.
Early Alzheimer's Disease
Donanemab(donanemab) AND AREA[Phase]PHASE38NCT05508789 · n = 1,500 · Eli Lilly and Company
Alzheimer Disease, Dementia, Brain Diseases
KarXT(xanomeline AND trospium) AND AREA[Phase]PHASE323NCT05304767 · n = 290 · Karuna Therapeutics, Inc., a Bristol Myers Squibb company
Schizophrenia
Zuranolone(zuranolone) AND AREA[Phase]PHASE38NCT03672175 · n = 581 · Biogen
Major Depressive Disorder
Esketamine(esketamine) AND AREA[Phase]PHASE330NCT03039192 · n = 226 · Janssen Research & Development, LLC
Depressive Disorder, Major
XPro1595(XPro1595) AND AREA[Phase]PHASE31NCT04370236 · n = 79 · Inmune Bio, Inc.
COVID-19

Where the numbers don't add up

  • The four in the Russian block add up to 0 registered studies. Noopept (0), phenylpiracetam (0), bromantane (0), and cortexin (0). The literature exists — 217 articles for cortexin alone — and the trial registration, in the international database, doesn't.
  • Dihexa and P021 are preclinical, and the database shows it. 18 and 45 articles, 0 and 0 registered studies. Whoever sells the two as a “next-generation nootropic” is selling a lab bench.
  • Lecanemab and donanemab have active registration in Brazil. LEQEMBI and KISUNLA, both in the biological category. It's the harshest contrast on this page: two hospital-infusion antibodies entered the Brazilian registration system while not a single nootropic did.
  • Esketamine has 8 active registrations, in two classes — injectable general anesthetic and antidepressant. Modafinil has 2. They are the only two stimulants/psychoactive drugs on this list with a legal product here, and the two are controlled prescriptions.
  • XPro1595's only phase 3 record is for COVID-19. 75 articles, 5 registered studies, 1 phase 3 — and that one is for pulmonary complications. The promise going around is neuroinflammation; the phase 3 record is a different matter.

In Brazil

I searched every active ingredient in the open data on registered medicines, downloaded on September 12, 2026 — 43,508 rows, counting only Active status. The therapeutic class column is the one the dataset itself declares.

The pattern is clean: the four in the Russian block, plus the xanomeline in KarXT and zuranolone, come back empty. Modafinil, esketamine, lecanemab, and donanemab have a product. Not being in the database isn't a ban — it's the absence of a legal product with that active ingredient.

Active ingredientSearch patternActive registrationsDeclared therapeutic classProducts
NoopeptNOOPEPT0
PhenylpiracetamFENILPIRACETAM0
BromantaneBROMANTAN0
CortexinCORTEXIN0
ModafinilMODAFINIL2OTHER PRODUCTS ACTING ON THE NERVOUS SYSTEMNUVIGIL, STAVIGILE
LecanemabLECANEMAB1OTHER PRODUCTS ACTING ON THE NERVOUS SYSTEMLEQEMBI
DonanemabDONANEMAB1OTHER ANTI-DEMENTIA MEDICATIONSKISUNLA
XanomelineXANOMELIN0
ZuranoloneZURANOLON0
EsketamineESCETAMIN8INJECTABLE GENERAL ANESTHETICS; ANTIDEPRESSANTSCLORIDRATO DE ESCETAMINA, KETAH, KETAH LC, KETAMIN, SPRAVATO

References

This page did not come from a secondary source. All the counts on this page were compiled by me on September 12, 2026, with the query stated next to each number. The four method caveats are written before the tables. This page was fact-checked on its own day, and so it carries its own date.
  1. Public ClinicalTrials.gov API, version 2 — the source for all the study and phase 3 counts on this page.
  2. PubMed E-utilities (esearch) — the basis for all article counts on this page.
  3. Registration NCT04370236 on ClinicalTrials.gov — INB03/XPro1595 in pulmonary complications of COVID-19, the only phase 3 the search returns.
  4. Registration NCT04468659 on ClinicalTrials.gov — lecanemab, sponsored by Eisai, one of the phase 3 trials the search returns.

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