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Randomized, Comparative, Double-blind, Placebo-controlled, Triple-dummy, Four-way Cross-over Study to Investigate Neurocognitive Effects of Brivaracetam in Healthy Subjects
The primary objective of the study is to evaluate the neurocognitive effects of brivaracetam
Age
18 - 50 years
Sex
ALL
Healthy Volunteers
Yes
Overland Park, Kansas, United States
Start Date
July 1, 2008
Primary Completion Date
October 1, 2008
Completion Date
October 1, 2008
Last Updated
May 28, 2012
20
ACTUAL participants
Brivaracetam
DRUG
levetiracetam
DRUG
lorazepam
DRUG
placebo
OTHER
Lead Sponsor
UCB Pharma
NCT06700356
NCT02531880
NCT05871372
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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