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Double-blind, Randomized Study Evaluating the Efficacy and Safety of Brivaracetam in Adults With Partial Onset Seizures

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UCB

Status and phase

Completed
Phase 3

Conditions

Epilepsy

Treatments

Drug: Brivaracetam
Other: Placebo

Study type

Interventional

Funder types

Industry

Identifiers

NCT00490035
2006-006344-59 (EudraCT Number)
N01252

Details and patient eligibility

About

This study will evaluate the efficacy and safety of Brivaracetam to support the submission file in the indication of adjunctive treatment in adolescents and adults with partial onset seizures.

Enrollment

399 patients

Sex

All

Ages

16 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subjects were from 16 to 70 years, both inclusive. Subjects under 18 years of age were only included where legally permitted and ethically accepted
  • Subjects with well-characterized focal epilepsy or epileptic syndrome according to the International League Against Epilepsy (ILAE) classification
  • Subjects had a history of partial onset seizures (POS) whether or not secondarily generalized (Type I seizures according to the ILAE classification)
  • Subjects had at least 2 POS whether or not secondarily generalized per month during the 3 months preceding Visit 1
  • Subjects had at least 8 POS whether or not secondarily generalized during the 8-Week Baseline Period
  • Subjects were uncontrolled while treated by 1 to 2 permitted concomitant antiepileptic drugs (AEDs). Vagal nerve stimulation was allowed and was not counted as a concomitant AED

Exclusion criteria

  • History or presence of seizures occurring only in clusters (too frequently or indistinctly separated to be reliably counted) before Visit 3
  • History or presence of status epilepticus during the year preceding Visit 1 or during Baseline

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

399 participants in 4 patient groups, including a placebo group

Placebo
Placebo Comparator group
Description:
Matching Placebo tablets administered twice a day
Treatment:
Other: Placebo
Brivaracetam 20 mg/day
Experimental group
Description:
Brivaracetam 20 mg/day, 10 mg administered twice a day
Treatment:
Drug: Brivaracetam
Drug: Brivaracetam
Drug: Brivaracetam
Brivaracetam 50 mg/day
Experimental group
Description:
Brivaracetam 50 mg/day, 25 mg administered twice a day
Treatment:
Drug: Brivaracetam
Drug: Brivaracetam
Drug: Brivaracetam
Brivaracetam 100 mg/day
Experimental group
Description:
Brivaracetam 100 mg/day, 50 mg administered twice a day
Treatment:
Drug: Brivaracetam
Drug: Brivaracetam
Drug: Brivaracetam

Trial contacts and locations

76

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Data sourced from clinicaltrials.gov

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