ID: cerebrolysin
Aliases: CEREBROLYSIN, porcine brain peptide mixture
Type: compound
Route/form: IV or IM injection in regional clinical use
Status: approved_in_some_countries
Evidence level: human RCT
Best data tier: human controlled/review; exact-use indirect
Support scope: human
Source types: human_rct, systematic_review
Linked sources: 3
Broad outcomes: Brain / mood / sleep
Reading note: These are curation notes anchored to linked sources, not a clinical recommendation or protocol.
Targets / mechanism
- neurotrophic peptide mixture
- stroke recovery and neurorehabilitation endpoints
- neuronal survival/plasticity hypotheses
Optimization domains
- brain
- stroke
- traumatic brain injury
- neurorehabilitation
- cognition
Research basis
- Multiple human trials exist in stroke/TBI rehabilitation contexts.
- More evidence-backed than typical nootropic research peptides, though still indication-specific.
Limits, risks, and missing evidence
- Systematic reviews have raised mixed efficacy and safety interpretation issues, including no clear all-cause mortality benefit in acute ischemic stroke.
- The Cochrane acute ischemic stroke review reports a potential increase in non-fatal serious adverse events.
- Disease rehabilitation trials should not be generalized to healthy cognitive enhancement.
Risk flags
- regional drug
- biologic extract
- disease specific evidence
- mixed systematic review context
- nonfatal sae signal
- medical supervision
Linked papers, labels, and reviews
- Cerebrolysin and Recovery After Stroke (CARS): a randomized, placebo-controlled, double-blind, multicenter trial
human_rct / pubmed_cerebrolysin_cars_2016
Human stroke recovery RCT; disease-specific neurorehabilitation context. - Cerebrolysin and repetitive transcranial magnetic stimulation in patients with traumatic brain injury: a randomized three-arm trial
human_rct / pubmed_cerebrolysin_tbi_2023
Human TBI trial; keep separate from generalized nootropic claims. - Cerebrolysin for acute ischaemic stroke
systematic_review / pubmed_cerebrolysin_stroke_review_2020
Cochrane systematic-review anchor; found no clear all-cause mortality benefit in acute ischemic stroke and a potential increase in non-fatal serious adverse events.