CognitiveNot FDA ApprovedClinical Trials

Cerebrolysin

Also known as FPE 1070

A neuropeptide mixture derived from porcine brain tissue, indicated for neurological conditions including stroke recovery, cognitive decline, and traumatic brain injury.

Approved in 40+ countries - Not FDA approved

Regulatory Pathway

Preclinical
Phase I
Phase II
Phase III
Phase IV
Approved

Dosing Protocol

Typical Dose

5-10 mL IV/IM daily for 10-20 days

Frequency

Daily during treatment cycles

Duration

10-20 day cycles

Community-reported dosing. Individual results vary. Not a medical recommendation.
Typical community protocol: 5-10 mL IV/IM daily for 10-20 days via Intravenous or intramuscular injection, Daily during treatment cycles. Dose range: 5-30 mL per day. Duration: 10-20 day cycles.

Timing & Administration

Administer via Intravenous or intramuscular injection. Frequency: Daily during treatment cycles.

Mechanism of Action

Contains neurotrophic factors that mimic BDNF, NGF, and CNTF activity. Enhances neuroplasticity, protects neurons from excitotoxicity, promotes neurogenesis, and improves synaptic function.

Research Summary

Evidence level: clinical trials. Clinical status: Approved in 40+ countries - Not FDA approved.

Side Effects & Safety

Important Warnings

  • Not approved in the US
Dizziness
headache
nausea
agitation
confusion
anaphylactic shock (rare)

References

No references available.