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PeptideWiki.bio

Cognitive

Cerebrolysin

Also called FPF-1070

InjectableEvidence AEvery day
Half-life
variesby component
Typical vial
30 / 50mg
Research amounts
30–50mg

per administration

Common schedule
Every day
Tested in people

A human trial worked out how much to take and how often, so a dosing schedule is shown.

Licensed as a medicine in roughly 40 countries.

The human evidence for Cerebrolysin used the intravenous route. The draw worked out here assumes a subcutaneous injection, so the amount is not a direct read-across.

Quick start

Cerebrolysin at a glance — the figures, plus how it's commonly run. Reference only, not medical advice.

Typical dose
30–50 mg per administration
How often
Every day
Where
Intravenous (clinical setting)
Storage
Dry vial kept cold and dark; a mixed vial in the fridge at 2–8 °C. Details

A research and community reference, not medical advice. Figures are descriptive, vary between sources, and are not a recommendation for use.

Work out your draw

These numbers are a starting point — change any of them.

Vial label

Copy this into your label printer.

Published research contexts for Cerebrolysin describe 3050 mg per administration. Descriptive only, not a recommendation.

A porcine-brain-derived mixture of low-molecular-weight peptides and free amino acids, not a single molecule, so no single elimination half-life describes it and none is modelled.

A porcine-brain-derived mixture of low-molecular-weight peptides and free amino acids, not a single defined molecule. It is supplied as a sterile solution and dosed by volume — about 30–50 mL given intravenously once daily for 10–21 days, at roughly 215 mg of peptide per mL — not as a milligram amount, so the vial sizes and dose range shown here are nominal placeholders for a calculator that expects milligrams. The human evidence used the intravenous route, so no subcutaneous schedule is established and no schedule table is shown.

Where these numbers come from

  • Heiss WD et al., Stroke 2012;43:630 (CASTA)Cerebrolysin 30 mL intravenously once daily for 10 days after acute ischemic stroke; the global outcome measure did not separate from placebo.

Next steps