Nootropic

Cerebrolysin

Controlled trials

Cerebrolysin is not a single peptide.

IMIntermediateApproved outside the USneuroprotectionfocus and cognitionlongevity

Also known as FPF-1070 · Cerebrolysin concentrate · Porcine brain peptide preparation

At a glance

Dose summary

Typical dose430.4 mg
Range215.2 mg–1076 mg
Frequency5 on, 2 off
Half-lifeUnknown
Schedule5 days on, 2 off
Cycle length4 weeks
RouteIM
Experience levelIntermediate
Evidence gradeControlled trials
ApprovalApproved outside the US
Where the dose comes fromAn approved product label

No reliable human half-life has been published for Cerebrolysin, so none is listed rather than guessed at.

Form

Supplied ready to use

Cerebrolysin is not a lyophilized powder. It arrives as a ready-made sterile solution in sealed ampoules, so there is no vial to mix, no bacteriostatic water to add and no concentration to work out — the dose is measured straight out of the ampoule. The figures listed as vial sizes are ampoule contents.

Mechanism & evidence

What it is, and what is known

Cerebrolysin is not a single peptide. It is a standardised enzymatic hydrolysate of purified porcine brain protein containing low-molecular-weight neuropeptides and free amino acids, so no single half-life or molecular weight applies. DOSING CONVENTION: it is supplied as a ready-made sterile solution at 215.2 mg of peptide concentrate per mL, in sealed ampoules of 1, 2, 5, 10 and 20 mL, and it is prescribed in mL, never in mcg.

The figures in this entry are the mg equivalents of that solution converted to mcg for consistency with the rest of the dataset: 215,200 mcg = 1 mL, 430,400 mcg = 2 mL, 1,076,000 mcg = 5 mL. It is NOT reconstituted, so the vial sizes above are ampoule contents and the bacteriostatic water field does not apply. Route matters: 5 mL is the practical ceiling for a single intramuscular injection, and the larger doses used in trials (10-50 mL/day) are given as slow intravenous infusions in a clinical setting, not IM.

It is approved in a number of European, Asian and CIS countries but is NOT FDA approved. Human evidence is more substantial than for the other compounds in this class - randomized trials and Cochrane reviews in acute ischaemic stroke, vascular dementia, Alzheimer disease and traumatic brain injury - but the results are mixed, the stroke reviews found no convincing benefit on death or dependency, and much of the trial base is manufacturer-sponsored.

Courses are conventionally given 5 days a week for about 4 weeks rather than continuously.

The caveat

Randomized trials and Cochrane reviews exist, but the results are mixed, the stroke reviews found no convincing benefit, and much of the trial base is manufacturer-sponsored.

Tolerability

Reported side effects

  • Injection site pain, burning or induration; volumes are large for an IM shot
  • Flushing or a sensation of warmth, worse with fast injection
  • Dizziness, headache
  • Agitation, restlessness or insomnia
  • Rarely, hypersensitivity reactions

Hard stops

Do not use this if

  • Pregnancy, possible pregnancy, or breastfeeding
  • Severe renal impairment
  • Under 18

These are flags, not a screening. They do not replace a conversation with a clinician who knows your history.

Handling

Storage

Sealed, as supplied48 months
Once opened1 day

Keep it cold, keep it dark, and label the vial with the date you mixed it. Discard anything cloudy or past the window above.

Combinations

Commonly stacked with

Stacking multiplies the side-effect surface and makes it impossible to tell which compound did what. Add one thing at a time.

References

Sources

Educational information only, not medical advice. Talk to a licensed clinician before starting, changing, or stopping anything.