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CERebrolysin In CADASIL — CERICA  

Cadasil Clinical Trial

Official title:
A Randomized, Double-blind, Single-centre, Two-period Cross-over, Placebo-controlled Trial on Safety and Efficacy in Patients With Genetically Proven CADASIL

Clinical Trial Summary

The objective of this trial is the global risk-benefit assessment of Cerebrolysin as compared to Placebo in patients with genetically proven CADASIL. In addition, a traditional approach will be taken based on an evaluation of the separate risk and benefit domains in comparison with placebo.

Clinical Trial Description

Safety data area collected throughout the study (adverse events, vital signs and laboratory tests) and thereafter in case of ongoing serious adverse events (SAEs) at study endpoint. Optional secondary parameters include analyses of biomarkers (samples of blood, hair, urine, and saliva). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05755997
Study type Interventional
Source Ever Neuro Pharma GmbH
Contact Stefan Winter, Ph.D.
Phone +1143 7665 20555
Email Stefan.Winter@everpharma.com
Status Recruiting
Phase Phase 2
Start date November 29, 2023
Completion date December 31, 2026
View Details
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