COMPOUNDS / PEPTIDE / CEREBROLYSIN
PEPTIDE

CEREBROLYSIN

MEDIUM RISK
BEST FOR:Cognition●●●●●●○○○○6/10
CEREBROLYSIN · CEREBROLYSINUM · CERE · CEREBROLYSIN CONCENTRATED SOLUTION
NootropicNeuroprotectivePeptide MixtureSoviet / RussianStroke Recovery

Porcine brain-derived peptide mixture used as a neuroprotective and nootropic agent in stroke and dementia, primarily in Eastern Europe and Asia.

ROUTE / DOSAGE
LOW1mL
STANDARD5mL
HIGH10mL
Note: Slower absorption; used when IV access is unavailable; daily for 10-21 days
CYCLE
10-20 day courses repeatable after rest periods
BIOAVAILABILITY
100% IV ~80-90% IM
ACTIVE DURATION
Days to weeks (cumulative course effect) (subjective)
STORAGE
Refrigerate at 2-8°C protect from light do not freeze
HALF-LIFE
Variable (peptide components degrade rapidly effects persist beyond elimination) (plasma)
DURATION BREAKDOWN
Total2-4 weeks (per treatment course)
OnsetDays (cumulative)
Come up1-2 weeks
Peak2-3 weeks
Offset1-2 weeks
After effectsWeeks to months
Duration varies by route, dose, and individual. Source: community reports.
§ 01 — EFFECTS
6 documented
Neuroprotective activity
Neurotrophic support
Improved cognitive function in vascular dementia
Promotes synaptic plasticity
Promotes neuronal survival
No proven mortality benefit in acute stroke
§ 02 — RISKS
Potential increase in non-fatal serious adverse events (moderate-certainty evidence)
Injection site reactions
Allergic/hypersensitivity reactions to porcine-derived proteins
Vertigo and sweating
Insomnia or agitation
No proven benefit on mortality in acute ischaemic stroke
§ 03 — INTERACTIONS
Interaction data not yet available for this compound.
§ 04 — SCIENCE

Cochrane reviews of Cerebrolysin for acute ischaemic stroke (7 RCTs, 1773 participants) found moderate-certainty evidence that it probably has no beneficial effect on all-cause death and no effect on total serious adverse events, but noted a potential increase in non-fatal serious adverse events, particularly at the 30 mL/day for 10 days dosing schedule. For vascular dementia, a Cochrane review (6 RCTs, 597 participants) found very low-quality evidence suggesting modest improvements in cognitive and global function, but studies had high risk of bias and heterogeneity. Many trials were industry-supported, and no studies reported quality of life or caregiver burden. Overall, the evidence base is weak and insufficient to confirm clinically meaningful benefit.

§ 06 — SOURCES
[1]
Cerebrolysin for acute ischaemic stroke (2023 Cochrane Review)
pubmed.ncbi.nlm.nih.gov ↗
[2]
Cerebrolysin for vascular dementia (2019 Cochrane Review)
pubmed.ncbi.nlm.nih.gov ↗
[3]
Cerebrolysin for acute ischaemic stroke (2020 Cochrane Review)
pubmed.ncbi.nlm.nih.gov ↗
[4]
Cerebrolysin for acute ischaemic stroke (2016 Cochrane Review)
pubmed.ncbi.nlm.nih.gov ↗
[5]
PubMed PMID 28430363
pubmed.ncbi.nlm.nih.gov ↗
[6]
PubMed PMID 30004268
pubmed.ncbi.nlm.nih.gov ↗
[7]
PubMed PMID 26083192
pubmed.ncbi.nlm.nih.gov ↗
[8]
PubMed PMID 30961868
pubmed.ncbi.nlm.nih.gov ↗
Disclaimer. Protokol.wiki is an informational reference. Nothing on this site is medical advice. Compounds listed may be unapproved, unregulated, or illegal in your jurisdiction. Consult a licensed physician before use. Data compiled from peer-reviewed literature.
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