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Clinical Trial Summary

The primary efficacy objective of the study is to determine if adjunctive therapy of natalizumab 300 mg intravenous (IV) every 4 weeks reduces the frequency of seizures in adult participants with drug-resistant focal epilepsy. The secondary efficacy objective is to assess the effects of natalizumab versus placebo in drug-resistant focal epilepsy on additional measures of seizure frequency.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03283371
Study type Interventional
Source Biogen
Contact
Status Completed
Phase Phase 2
Start date March 20, 2018
Completion date November 18, 2020