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A Multicenter, Double-blind, Randomized, Placebo-controlled, 4 Parallel Groups, Dose-ranging Trial Evaluating the Efficacy and Safety of Brivaracetam Used as Adjunctive Treatment at Doses of 5, 20 and 50 mg/Day in b.i.d. Administration (Oral Tablets of 2.5 or 10 mg) for a Maximum of 7 Weeks in Subjects From 16 to 65 Years With Refractory Epilepsy Suffering From Partial Onset Seizures Whether or Not Secondarily Generalized
This trial will evaluate the efficacy and safety of brivaracetam (at doses of 5, 20 and 50 mg/day in twice a day administration) as add-on therapy in subjects with focal epilepsy.
Age
16 - 65 years
Sex
ALL
Healthy Volunteers
No
Phoenix, Arizona, United States
Little Rock, Arkansas, United States
Fresno, California, United States
Bradenton, Florida, United States
Jacksonville, Florida, United States
Chicago, Illinois, United States
Paducah, Kentucky, United States
Ruston, Louisiana, United States
Bethesda, Maryland, United States
Burlington, Massachusetts, United States
Start Date
November 7, 2005
Primary Completion Date
June 29, 2006
Completion Date
June 29, 2006
Last Updated
October 2, 2018
210
ACTUAL participants
Placebo
OTHER
Brivaracetam
DRUG
Lead Sponsor
UCB Pharma
NCT06700356
NCT02531880
NCT05871372
Data Source & Attribution
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