CerebrolysinNeurotrophic Peptide MixtureBlendSafety Rating 6/10

Primary research areaNeurotrophic research

Research-literature reference data, NOT patient instructions. Not for human use. Consult a licensed clinician for any human application.

Research dose range10–30 mL/day IV (stroke/AD trials)source ↗
AdministrationIV infusion (diluted in saline) or IM injection
Half-lifeNot well characterized (mixture of peptides)
Safety6/10 · Approved in some countries
NCAA D1Not listed

Price Comparison

Compare vendors

2 vendors competing

VendorPrice$ / mgUpdated
Pantheon PeptidesBest $/mgCOA ✓ · 3P$55.08$61.20−10% · code PEPTIDEPRI10$0.92Apr 23, 2026Buy →
Polar PeptidesCOA on request$143.99$2.40Apr 17, 2026Buy →

Overview

About Cerebrolysin

Mechanism of action

Mixture of low molecular weight neuropeptides and amino acids; mimics neurotrophic factors (BDNF, NGF, CNTF); promotes neurogenesis, synaptogenesis, and neuroprotection; BBB-penetrant.

Safety profile

Injection site reactions; dizziness; agitation with high doses; rare allergic reactions. Very well-studied with good long-term safety data. · Used in Europe/Asia for stroke/TBI; some clinical trial data; not FDA-approved but prescribed widely abroad

Storage

Stability & handling

❄️Lyophilized (powder)Supplied as solution — see labeling
💉Reconstituted2–8°Cper labeling
📈

Price tracking starts now.

Set an alert to get notified when this peptide drops.

Related pages

More on Cerebrolysin

Stack & Compare

Frequently Researched Together

Research

Studies & key findings

  • Cerebrolysin is a standardized porcine brain-derived peptide mixture containing low-molecular-weight neuropeptides with BDNF-like and NGF-like activity; it is widely approved and used in Russia, Eastern Europe, China, and parts of Asia for stroke, vascular dementia, and Alzheimer's disease, though it lacks full regulatory approval in the US and Western Europe.
  • A 2016 randomized Phase II trial (CARS) in acute ischemic stroke patients found Cerebrolysin produced significantly better upper extremity motor recovery than placebo at 90 days (effect size 0.71, p<0.0001); a 2018 meta-analysis of nine RCTs confirmed statistically significant neurological improvement at 30 days, with a number needed to treat of approximately 8.

6 peer-reviewed sources cited — clinical, preclinical, and regulatory.

Read full research →
Failed to fetch