drugset / Trial / NCT01822951

Cerebrolysin Compared to Donepezil in Patients With Mild to Moderate Dementia of Alzheimer's Type (DAT)

NCT01822951

Phase 4 Withdrawn Ever Neuro Pharma GmbH
RandomizedParallel-groupTriple-blindTreatment

Summary

The objective of this trial is the global risk-benefit assessment of Cerebrolysin as compared to donepezil in patients with mild to moderate dementia of Alzheimer's Type (DAT). In addition, a traditional approach will be taken based on the evaluation of the separate risk and benefit domains in comparison with donepezil. Global risk-benefit as compared to donepezil will be analyzed by determining whether the Cerebrolysin group shows a statistically significant non-inferiority with regard to the combined primary safety and efficacy endpoints (weighted multivariate ensemble). The endpoints will be combined by a global multivariate non-parametric procedure, weighting the safety and efficacy part 50:50.

Timeline

Start
Primary completion
2016-09
Completion
2016-12

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Cerebrolysin Peptide 20 ml Intravenous
Comparator Donepezil Small molecule 10 mg Oral

Indications