drugset / Trial / NCT00630968

S.K.A.T.E.: Safety of Keppra as Adjunctive Therapy in Epilepsy

NCT00630968

Phase 4 Completed 1541 enrolled UCB Pharma
Non-randomizedSingle-groupOpen-labelTreatment

Summary

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.

Timeline

Start
2000-08
Primary completion
2004-02
Completion
2004-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Levetiracetam Other / unclassified 1000 mg

Indications