Approved outside the US

Semax Dosage Chart

Clinic/vendor intranasal protocol and source limits for the Russian-approved cognitive and neuroprotective peptide.

Written by
Megan Williams
Editor-in-Chief
Fact-checked by
Brian Williams
Co-founder & Research Editor
Last updated
August 25, 2026

Fact-checking at PeptideProbe is editorial, not clinical. Our editors check claims, dosing figures, and trial results against primary sources; they are not licensed clinicians and do not provide medical review. Nothing here is medical advice — talk to a qualified healthcare provider before starting any therapy.

Educational tool — not medical advice. This calculator provides estimates based on population averages and published trial data. Outputs are not clinical recommendations and do not replace evaluation by a qualified prescriber. Do not start, stop, or change a peptide therapy based on the result of this tool.

Semax is a synthetic analog of ACTH (4-10) developed at Russia's Institute of Molecular Genetics. It is approved in Russia for stroke recovery, cognitive impairment, and as a nootropic. Mechanism studies describe BDNF/trkB and neuroprotective effects, but it is not FDA-approved in the US. On July 24, 2026, FDA's Pharmacy Compounding Advisory Committee recommended Semax-related bulk drug substances for the 503A Bulks List; that vote is advisory only, is not approval, and has not changed federal legal status.

Semax at a Glance

Clinic/vendor dose200–600 mcg per nostril (total 400–1,200 mcg per dose)
Frequency2–3× per day intranasal
Course length10–14 days, repeated as needed (not source-derived)
RouteIntranasal spray
FDA statusNot FDA-approved. Russian-approved; July 2026 PCAC recommendation is advisory only and legally unchanged.
Source qualityMechanism studies plus Russian-language clinical stroke literature; no English replicated dose-ranging trial.

Semax Dosing by Use Case

Commonly cited protocols vary by what Semax is being used for. The table below summarizes typical ranges reported in clinical practice and published literature.

Use caseTypical doseFrequencyCycle lengthNotes
Cognitive support / nootropic400–600 mcg total per dose2× daily intranasal10–14 days, may repeat after 2 weeks offCommon clinic/vendor convention; not established by the cited literature.
Acute ischemic stroke (Russian clinical literature)12–18 mg/day in the cited 1997 studyDivided intranasal dosing under supervision5 days for moderate stroke; 10 days for severe stroke in the cited studyClinical setting only; this does not validate nootropic microgram protocols.
ADHD / focus support (off-label)400 mcg total per doseMorning + midday intranasal2 weeks on, 2 weeks offOff-label clinic/vendor convention; not validated in Western trials.

Stacking Semax

Semax and Selank are sometimes alternated for combined nootropic + anxiolytic support. Co-administration is less common than alternating cycles.

Where these numbers come from

The cited Semax literature supports a limited evidence base, not the intranasal nootropic protocol printed here. Two 2006 Dolotov papers and the 2025 Filippenkov paper are mechanism/animal studies involving BDNF, trkB, gene-expression, and ischemia models. The human clinical citation is a Russian-language acute ischemic stroke study, with a much higher supervised stroke regimen than the microgram nootropic doses clinics and vendors commonly print. None of these sources establishes 200-600 mcg per nostril, 2-3x daily, 10-14 day nootropic or focus protocols, and the trial literature has not been independently replicated in English-language journals. Semax is approved in Russia but not FDA-approved in the US; the July 2026 PCAC recommendation for the 503A Bulks List is advisory only, is not approval, and has not changed federal legal status.

Safety profile

Semax has limited Russian clinical safety data and sparse Western validation.

  • Common side effects: mild nasal irritation; rare reports of headache or transient blood pressure changes.
  • Does not produce sedation or stimulant-like dependence in published data.
  • Long-term continuous use beyond labeled course lengths is not well-studied.
  • Not FDA-approved.
Do not use if
  • Pregnancy or breastfeeding
  • Active sinusitis or nasal pathology (avoid intranasal route)
  • Bipolar disorder or active mania (theoretical concern with dopaminergic modulation)

Semax Dosing FAQ

Mechanism studies measured neurotrophin changes within hours after intranasal dosing in animals. Human onset claims for nootropic use are not well established in English-language trials; clinic protocols usually use short courses rather than continuous daily use.

The cited sources do not establish dependence or withdrawal. That is not the same as a long-term safety study, so repeated courses should be clinician-supervised.

Sources

Related Dosage Charts

Where to get Semax with a prescription

Semax requires a prescription and medical supervision. Each service below states that a licensed provider reviews your intake and prescribes through a US compounding pharmacy where appropriate. Those are the companies’ own descriptions of how they operate, not findings of ours. Compounded medications are not FDA-approved, and a consultation does not guarantee a prescription.

Some telehealth links below are affiliate links. If you buy through them, we may earn a commission at no extra cost to you. Commission never affects which products or clinics we list, how they are ordered, or what we say about them — see our editorial policy.

HealthRx — telehealth consultationAd

Says a board-certified physician reviews each intake and prescribes through a licensed 503A compounding pharmacy where appropriate, and lists a LegitScript certification. Compounded medications are not FDA-approved.

We are not a clinic and do not prescribe. Listing a service here is not a clinical endorsement of it, and you should confirm licensure and pharmacy sourcing yourself before treatment.

Want the full Semax guide?

Mechanism, clinical evidence, side effects, costs, and provider listings for Semax therapy.

Medical Disclaimer: This content is for informational purposes only and should not be considered medical advice. Always consult with a qualified healthcare provider before beginning any peptide therapy treatment.