A 12-week, multi-center,randomized, double-blind, placebo-controlled efficacy and safety study examining seizure frequency of BGG492 capsules administration orally three times daily (TID) as adjunctiv...

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Reference: EUCTR2009-017961-52

A 12-week, multi-center,randomized, double-blind, placebo-controlled efficacy and safety study examining seizure frequency of BGG492 capsules administration orally three times daily (TID) as adjunctive treatment in patients with partial onset seizures

Woman and Man

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Extract

Detect a dose-response of BGG492 as measured by change in seizure frequency from the 4-week baseline period (week -4 to .1) to the 4-week double-blind maintenance period (weeks 7 to 10).


Inclusion criteria

  • refractory partial-onset seizures