The purposes of the study were to obtain further information about the optimal dose and the efficacy of Keppra in daily clinical practice, and to confirm the favorable safety and tolerability profiles of the drug observed during clinical development.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
1,541
Percentage reduction in seizure frequency.
Time frame: 16-week treatment period
To further assess safety.
The patient-weighted Quality Of Life In Epilepsy inventory.
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