Semax Labs

Compounded, not FDA-approved

The same molecule is stroke medicine in Moscow and a research chemical in Miami

Semax has been described in peer-reviewed journals as a registered Russian nootropic used to treat ischemic stroke, and in the United States it has no approved product at all: in July 2026 FDA proposed that it not even be allowed into compounded drugs. Both of those are true, and the gap between them is not a conspiracy. It is a translation problem. Of the 206 papers indexed on this peptide, 83 are in Russian and 50 are indexed with an English abstract and nothing else, so most of the evidence cannot be read by the people arguing about it. Exactly one record in the entire literature carries a randomized-controlled-trial tag, and it is a 27-patient motor neuron disease study. Every row in our evidence table is labeled by species, and every human row is labeled by the language it was published in.

  • 206papers indexed on semax in Europe PMC
  • 83of them published in Russian, which is 40.3 percent of everything written about this peptide
  • 1carries a randomized-controlled-trial tag, and it studied 27 patients with motor neuron disease
  • 26rows in our evidence table, each labeled by species, including 4 documented absences of evidence
  • 41fetch-verified citations, 100.0 percent peer-reviewed or government sources

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Semax nasal spray care, made simple

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Compounded nasal sprayPrepared after approval
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Key facts

  • StatusCompounded, not FDA-approved
  • Human half-lifeNot establishedsource
  • Human intranasal bioavailabilityNot establishedsource
  • Human Cmax or AUCNot establishedsource
  • Published human PK studies0source
  • Animal brain access (rat, intranasal)Demonstrated by membrane binding and gene expression change within 1 hoursource
  • Animal effective dose used in mechanism work50 micrograms per kilogram (rat)source
  • In vitro potency, human serum enkephalinase inhibitionIC50 10 micromolarsource
  • ClassSynthetic heptapeptide; ACTH(4-7) fragment extended with Pro-Gly-ProChemical referencesource
  • SequenceMet-Glu-His-Phe-Pro-Gly-Pro (MEHFPGP)Chemical referencesource
  • Molecular weight813.9 Da (C37H51N9O10S)Chemical referencesource
  • CAS80714-61-0Chemical referencesource
  • US FDA statusNot approved for any use; on FDA's compounding safety-risks listRegulatory recordsource
  • July 2026 PCACFDA proposed semax NOT be added to the 503A Bulks ListRegulatory recordsource
  • Route in the literatureIntranasal (0.1 and 1 percent solutions); endonasal electrophoresis in ophthalmology studiesReview or guidelinesource
  • Indexed literature206 Europe PMC records; 83 Russian-language (40.3 percent)Analytical studysource
  • English abstract only50 records: the abstract is all a non-Russian reader can readAnalytical studysource
  • Randomized controlled trials1 in the entire literature (27 patients, motor neuron disease, Russian)Analytical studysource
  • Double-blind studies0Absence of evidencesource
  • Meta-analyses and systematic reviews0Absence of evidencesource
  • Registered trials (ClinicalTrials.gov)0Absence of evidencesource
  • Human pharmacokineticsNone publishedAbsence of evidencesource
  • Established human doseNone; published regimens disagree by orders of magnitudeAbsence of evidencesource
  • Russian statusDescribed in peer-reviewed literature as a registered Russian nootropic; registration not verified against the state registerReview or guidelinesource
  • Anti-doping statusUnclear; a 2025 anti-doping review pairs semax with tetracosactide (WADA class S2)Review or guidelinesource

Read the full Semax monograph

Browse by topic

Everything on Semax, organized the way you research it.

All guides

51 in-depth, individually cited guides.

Dosing 14 guides

Evidence 11 guides

Sourcing 10 guides

Safety 9 guides

Comparisons 7 guides

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