7-residue chain
Tuftsin-derived heptapeptide; registered in Russia as a nasal anxiolytic
Selank is approved in Russia (not by FDA/EMA/MHRA) as an anti-anxiety agent, marketed as a 0.15% intranasal formulation. The official Russian label could not be retrieved, so no label dose is encoded. Injectable vial use is community practice.
Short community courserecommended
Community practice, not from a label or trial: within the 100-500 mcg/day subcutaneous range, with a 10-14 day clinical-style course length.
Longer, upper-range community course
Community practice, not from a label or trial: top of the 100-500 mcg/day subcutaneous range, for a 2-4 week course.
Route: Intranasal is the studied and marketed route. Reconstituting a lyophilized vial for subcutaneous injection (or nasal use) is community use, not from a label or trial.
Timing: No reliable figure found in the sources; ask your prescriber or supplier.
No reliable figure found in the sources; ask your prescriber or supplier.
Courses in the source run from 10-14 days to 2-4 weeks; no sourced rest period.
Why:
Approved only in Russia (GAD and neurasthenia, nasal). Not FDA-, EMA- or MHRA-approved; not on the US 503A bulks list per Superpower; WADA S0 per Outliyr. Online vials have no quality oversight.
Common side effects:
Stop and call your prescriber if:
Labs and monitoring:
What sources report this compound changes, or say to check. A record of the evidence, not targets or advice.
Shifted in patients with generalised anxiety disorder and neurasthenia after 14 days of Selank; in vitro, IL-6 expression was suppressed in blood from depressed patients only. The abstract gives no figures.
PubMed 18577961: Immunomodulatory effects of selank in anxiety-asthenic disorders