single10MG
Semax
10MG Protocol
Semax 10MG
Injection Freq.
Inject once daily
Cycle Sched.
8 weeks continuous; optional extension to 12–16 weeks with off‑periods (e
Reconstitution
3.0 mL BAC water
Support for attention, memory consolidation, and learning in cognitive-deficit populations
Studied in stroke/TBI/optic neuropathy with favorable safety profiles in month-long trials
Dose-dependent effects
titration helps find minimum effective exposure
1
Reconstitution Requirements
- 3.0 mL BAC water
| Step | Week Range | Dose | Units |
|---|---|---|---|
| 1 | Weeks 1–2 | 300 mcg | 9 |
| 2 | Weeks 3–4 | 500 mcg | 15 |
| 3 | Weeks 5–6 | 600 mcg | 18 |
| 4 | Weeks 7–8 | 800 mcg | 24 |
Inject once daily
8 weeks continuous; optional extension to 12–16 weeks with off‑periods (e
Semax is described as a synthetic analog of the ACTH(4–10) fragment with a C-terminal Pro-Gly-Pro extension that increases metabolic stability. In the protocol’s mechanism section, Semax is presented as a neuroactive peptide that influences neurotrophic and neurotransmitter pathways relevant to cognition and recovery. Specifically, the page describes modulation of brain-derived neurotrophic factor (BDNF) expression, support of neuronal survival, and effects on monoaminergic systems; other sections discuss cholinergic and dopaminergic neurotransmission in the broader literature. Human use described in cited clinical work is primarily intranasal, including research in cognitive impairment and stroke recovery, but the protocol notes that subcutaneous administration can serve as a practical alternative with potentially more sustained systemic absorption that supports once-daily dosing. Overall, Semax is framed as a nootropic/neuroprotective peptide that supports neuroplasticity and resilience through BDNF-linked and monoamine-linked signaling.
Mild injection-site reactions (redness/itching)
Generally well tolerated
no significant adverse effects reported at standard doses in cited studies
- Use aseptic technique: wipe vial stopper with alcohol; use new sterile syringe/needle
- Add diluent slowly down the vial wall to minimize foaming
- Gently swirl/roll until fully dissolved (do not shake)
- Label vial with reconstitution date and concentration; protect from light
- Refrigerate after reconstitution (commonly 2–8 °C) unless protocol states otherwise
- Avoid repeated freeze–thaw cycles
- Bacteriostatic Water for Injection contains benzyl alcohol preservative (multi-dose); follow protocol for beyond-use (many peptide protocols use ~28 days after mixing)
- Avoid benzyl-alcohol-containing diluents in neonates/infants (safety warning for benzyl alcohol)