An Open-label, Multinational, Multicenter, Follow-up Study to Evaluate the Long-term Safety and Efficacy of Brivaracetam
Status: | Completed |
---|---|
Conditions: | Neurology, Epilepsy |
Therapuetic Areas: | Neurology, Other |
Healthy: | No |
Age Range: | 16 - Any |
Updated: | 7/13/2018 |
Start Date: | November 2008 |
End Date: | March 2017 |
An Open-label, Multinational, Multicenter, Follow-up Study to Evaluate the Long-term Safety and Efficacy of Brivaracetam Used at a Flexible Dose up to a Maximum of 200 mg/Day in Subjects Aged 16 Years or Older Suffering From Epilepsy.
The Sponsor wishes to develop brivaracetam as an anti-epileptic treatment in subjects 16
years and older with epilepsy. This study permits continued access to treatment for subjects
who participated in a previous epilepsy study. The study will explore the long-term safety
and efficacy of brivaracetam.
years and older with epilepsy. This study permits continued access to treatment for subjects
who participated in a previous epilepsy study. The study will explore the long-term safety
and efficacy of brivaracetam.
Inclusion Criteria:
- Subjects with epilepsy who participated in previous brivaracetam trials which allow
access to the present trial.
- Subjects from whom the Investigator believes a reasonable potential benefit from the
long-term administration of brivaracetam may be expected.
Exclusion Criteria:
• Severe medical, neurological and psychiatric disorders, including current suicidal
ideation or behaviour, or laboratory values which may have an impact on the safety of the
subject, as determined by the investigator.
We found this trial at
26
sites
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