A Study Of The Safety And Efficacy Of Levetiracetam (Keppra®) (Ucb L059) In Children With Epilepsy
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|ClinicalTrials.gov Identifier: NCT00150709|
Recruitment Status : Completed
First Posted : September 8, 2005
Last Update Posted : February 15, 2017
|Condition or disease||Intervention/treatment||Phase|
|Epilepsy, Partial||Drug: Levetiracetam (Keppra)||Phase 3|
|Study Type :||Interventional (Clinical Trial)|
|Enrollment :||238 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||A Multi-Center, Open-Label, Long-Term, Follow-Up Study Of The Safety And Efficacy Of Levetiracetam (Ucb L059) In Children With Epilepsy|
|Study Start Date :||February 1998|
|Actual Primary Completion Date :||January 2006|
|Actual Study Completion Date :||January 2006|
- To allow pediatric patients who have participated in a previous trials the opportunity to receive open-label levetiracetam (Keppra) treatment.
- Efficacy measured by weekly seizure frequency.
- To obtain standardized descriptive safety and efficacy data in pediatric epileptic patients
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00150709
|Study Director:||UCB Clinical Trial Call Center||UCB Pharma|