Cognition
Semax
ACTH(4-7)-Pro-Gly-Pro
Semax is a synthetic peptide built from a fragment of the hormone ACTH, developed and studied mainly in Russia. It is not FDA-approved, and most of its clinical literature has not been replicated in Western trials.
Key facts
- Commonly discussed for: focus, memory and stroke recovery.
- Evidence (C): Human data come mostly from Russian clinical studies, such as a 2018 study of 110 ischemic-stroke patients comparing rehabilitation with and without Semax. These are small and not large, independently replicated randomized trials.
- FDA status: PCAC recommended. On July 24, 2026 the PCAC voted 8-5 (1 abstention) to recommend Semax for the 503A Bulks List for cerebral ischemia, migraine and trigeminal neuralgia; FDA must still publish a proposed rule; none appeared in the Federal Register as of October 1, 2026.
- Legitimate access: No clear legal route yet.
- Last reviewed: October 1, 2026.
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Open my stack →Sources
- Gusev et al. The efficacy of Semax in patients at different stages of ischemic stroke. Zh Nevrol Psikhiatr, 2018
- Effectiveness of Semax in the acute period of hemispheric ischemic stroke. Zh Nevrol Psikhiatr, 1997
- McDermott Will & Schulte: PCAC backs majority of peptides in two-day public meeting (July 2026)
- Federal Register notice of PCAC meeting and uses under review (April 16, 2026)