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Cognitive & NeuroGrade DWeak, conflicting or negative3 primary sources

Cerebrolysin

Also known as FPF-1070 · porcine brain peptide preparation

A mixture of low-molecular-weight peptides from pig brain, licensed in parts of Europe and Asia for stroke and dementia. Large trials have been repeatedly inconclusive.

Overview

Cerebrolysin is not one molecule. It is a standardised extract of enzymatically broken-down pig brain tissue, containing a mixture of short peptides and free amino acids. The claim is that it mimics the action of the body's own neurotrophic factors — the signals that keep neurons alive and encourage them to form connections. The evidence has never been decisive: individual trials report benefit, large well-controlled trials tend to report much less, and meta-analyses come out cautious.

Research areas

Ischaemic strokeTraumatic brain injuryVascular dementia

Community-specified data

Community dosage information

Unverified
Community protocol

Cerebrolysin 30mg

Third-party
01Reconstitution solution
3 mL
02Dose
5 mg
03Syringe units
50 units
04Frequency
7x/week
05Cycle length
30 days
06Bacteriostatic water
3 mL
07Bottle size
30 mg
08Bottles needed
5

Source note: 30-day cycles, 5x/year

Track this schedule

Not medical guidance. These third-party figures have not been independently verified, clinically reviewed, or endorsed by DB Peptide. They may be inaccurate or unsafe and should not replace product labelling or advice from a qualified clinician.

Dosing reported in the literature

Every protocol below is reproduced from a published study or approved labelling, with its source named. These are records of what was studied — not recommendations, and not a suggestion that any of them is appropriate for any person.

Protocol as reportedSource
30 ml daily by intravenous infusion for 10 days, starting within 12 hours of stroke onsetThe trial did not demonstrate a significant benefit on its primary endpoint.CASTA trial protocol
30 ml daily for 21 days in traumatic brain injury rehabilitation studiesTBI rehabilitation trial literature

Trial status

Numerous randomised trials in stroke, TBI and dementia, with inconsistent results and a negative Cochrane assessment in acute stroke.

Reported safety signals

  • Generally well tolerated in trials, with dizziness, agitation and injection-site reactions reported.
  • Being a porcine tissue-derived biological, hypersensitivity reactions are a genuine consideration.
  • Contraindicated in status epilepticus and severe renal impairment per its European labelling.
  • Batch composition is not identical between production lots, which complicates any interpretation of trial results.

Common questions

Why is the evidence so mixed?

Two structural reasons. It is a biological hydrolysate whose exact composition varies between batches, so trials are not testing an identical product. And much of the positive literature comes from smaller trials in specific regions, while the largest and most rigorously controlled trials have generally been null.

Primary sources

3 citations
  1. 01

    Cerebrolysin for acute ischaemic stroke

    Cochrane Database of Systematic Reviews2020

  2. 02

    Cerebrolysin in patients with acute ischemic stroke in Asia: results of a double-blind, placebo-controlled randomized trial

    Stroke2012

  3. 03

    Cerebrolysin in vascular dementia: improvement of clinical outcome in a randomized, double-blind, placebo-controlled multicenter trial

    Journal of Neural Transmission2011

Medical disclaimer

This page is for informational and research purposes only. Nothing here constitutes medical advice. The compounds discussed are research chemicals. Consult a qualified clinician before starting any protocol.

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