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Completed Phase 3 Interventional Results available

An Open-label, Multinational, Multicenter, Follow-up Study to Evaluate the Long-term Safety and Efficacy of Brivaracetam

ClinicalTrials.gov ID: NCT00761774

Public ClinicalTrials.gov record NCT00761774. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 12:20 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

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.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT00761774
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
UCB Pharma
Industry
Enrollment
108 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
16 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 2008 (Type not available)
Primary completion
Mar 2017 (Actual)
Completion
Mar 2017 (Actual)
Last update posted
Jul 11, 2018

2008 – 2017

United States locations

U.S. sites
25
U.S. states
18
U.S. cities
25
Facility City State ZIP Site status
304 Phoenix Arizona — —
281 Fresno California — —
288 Pasadena California — —
240 Riverside California — —
245 Sacramento California — —
285 Peoria Illinois — —
224 Indianapolis Indiana — —
266 Lexington Kentucky — —
231 Waldorf Maryland — —
278 Burlington Massachusetts — —
270 New York New York — —
284 Hickory North Carolina — —
241 Columbus Ohio — —
265 Oklahoma City Oklahoma — —
297 Germantown Tennessee — —
260 Austin Texas — —
236 Bedford Texas — —
267 Dallas Texas — —
268 Houston Texas — —
211 Layton Utah — —
235 Ogden Utah — —
218 Burlington Vermont — —
279 Danville Virginia — —
277 Charleston West Virginia — —
213 Marshfield Wisconsin — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 33 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00761774, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 11, 2018 · Synced Oct 21, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00761774 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →