Levetiracetam 250 mg
Drug- Active Substance: Levetiracetam
- Pharmaceutical Form: Film-coated tablet
- Concentration: 250 mg
- Route of Administration: Oral Use
Other names: Keppra
NCT Number: NCT00280696
A double-blind, randomized, multicenter, placebo controlled 5 parallel groups, confirmatory trial to evaluated the efficacy and safety of levetiracetam used as adjunctive treatment in patients from 16 to 65 years with epilepsy suffering from partial onset seizures.
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Notify Me16 year–65 year
All sexes
Interventional
Phase 3
Aichi-gun, Aichi-ken, Japan
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Epileptic patients who fulfill the following criteria are eligible for inclusion in the study:
Exclusion criteria
The following patients are not eligible for inclusion into the study:
Other names: Keppra
Other names: Keppra
Time frame: From Baseline to the 12-week Evaluation Period
Time frame: 12-week Evaluation Period
Time frame: From Baseline to the 12-week Evaluation Period
Time frame: 12-week Evaluation Period
Time frame: From Baseline to the 12-week Evaluation Period
Time frame: From Baseline to the 12-week Evaluation Period
UCB Japan Co. Ltd.
Industry
A Double-blind, Randomized, Placebo-controlled 5 Parallel Groups, Confirmatory Trial on the Efficacy and Safety of Levetiracetam Used as add-on Therapy at Doses of 0.5 to 3 g/Day in Patients From 16 to 65 Years With Epilepsy With Partial Onset Seizures Under Treatment With 1 to 3 Anti-epileptic Drug(s)
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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