Content reviewed by clinical research staff

Last reviewed: March 2026Sources: PubMed, FDA, WADA Prohibited List

Evidence graded using the PeptideScholar A-D system

Cerebrolysin

BHuman Studies
55
Moderate Credibility
1 cited studyy · Evidence level B

Neuropeptide preparation (porcine brain-derived) · Brand: Cerebrolysin

Not FDA ApprovedPrescription Required

Cerebrolysin is a parenteral neuropeptide preparation produced from purified porcine brain proteins. It contains a mixture of low-molecular-weight peptides and free amino acids with neurotrophic activity. Approved for use in several countries for dementia and stroke recovery, though not FDA-approved.

Mechanism of Action

Contains neurotrophic factors including BDNF-like and CNTF-like peptides that promote neuronal survival, synaptic plasticity, and neurogenesis. Stimulates protein synthesis in neurons, reduces excitotoxicity, and inhibits amyloid aggregation. Also has anti-inflammatory and antioxidant properties in the CNS.

Benefits

  • Improves cognitive function in vascular dementia and Alzheimer's disease
  • May enhance recovery after acute ischemic stroke[1]
  • Neuroprotective via multiple mechanisms (anti-apoptotic, anti-inflammatory)
  • Extensive clinical use outside the US with established safety profile
Not Medical Advice — Research-Reported Information Only

This content is for informational purposes only and does not constitute medical advice.

Cerebrolysin — Dosing in Published Research

Reported Routes: Intravenous, Intramuscular injection
Typically 10-30 mL IV or IM daily for 10-20 days, followed by maintenance dosing. Used in post-acute stroke, traumatic brain injury, and dementia protocols in Europe, Asia, and Latin America. Not available in the US.

The dosing information above is sourced from published research literature and clinical trials. These are not recommendations. Individual responses vary. Always consult a healthcare provider before considering any peptide-based therapy.

Side Effects

  • Dizziness and headache
  • Nausea and sweating
  • Injection site reactions
  • Rare allergic reactions (porcine-derived product)
  • Potential risk of prion transmission (theoretical; no cases reported)

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Cerebrolysin is not FDA-approved. Always consult a licensed healthcare provider before considering any peptide.

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Research & Evidence

ReviewCochrane Database Syst Rev, 2023

Cerebrolysin for acute ischaemic stroke.

Cochrane review found cerebrolysin may improve functional outcomes in acute ischemic stroke, but evidence quality was low to moderate; more rigorous trials needed

PMID: 37818733

References

  1. 1. Cerebrolysin for acute ischaemic stroke.. Cochrane Database Syst Rev, 2023. Cochrane review found cerebrolysin may improve functional outcomes in acute ischemic stroke, but evidence quality was low to moderate; more rigorous trials needed [PMID: 37818733]

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Cerebrolysin FAQ

Medical Disclaimer

This content is for informational and educational purposes only and does not constitute medical advice, diagnosis, or treatment recommendations.

Always consult a qualified healthcare provider before starting, stopping, or modifying any treatment. Do not disregard professional medical advice based on information found on this site.

No claims of therapeutic efficacy are made for substances that are not FDA-approved for the discussed indications. Research citations reflect published findings and do not imply endorsement.

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