Open-Label Extension Study to Assess the Safety and Seizure Frequency Associated With Lacosamide for Primary Generalized Tonic-Clonic Seizures in Subjects With Epilepsy
Public ClinicalTrials.gov record NCT01118962. 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.
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 Extension Study to Assess the Safety and Seizure Frequency Associated With Long-Term Oral Lacosamide for Uncontrolled Primary Generalized Tonic-Clonic Seizures in Subjects With Idiopathic Generalized Epilepsy
Study identification
- NCT ID
- NCT01118962
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 2
- Lead sponsor
- UCB BIOSCIENCES, Inc.
- Industry
- Enrollment
- 39 participants
Conditions and interventions
Conditions
Interventions
- Lacosamide Drug
Drug
Eligibility (public fields only)
- Age range
- 16 Years to 65 Years
- 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
- Jul 31, 2010
- Primary completion
- Sep 30, 2012
- Completion
- Sep 30, 2012
- Last update posted
- Jul 16, 2018
2010 – 2012
United States locations
- U.S. sites
- 19
- U.S. states
- 18
- U.S. cities
- 19
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| 603 | Phoenix | Arizona | — | — |
| 602 | Little Rock | Arkansas | — | — |
| 628 | Aurora | Colorado | — | — |
| 613 | Atlanta | Georgia | — | — |
| 617 | Boise | Idaho | — | — |
| 614 | Fort Wayne | Indiana | — | — |
| 605 | Lexington | Kentucky | — | — |
| 616 | Louisville | Kentucky | — | — |
| 619 | Scarborough | Maine | — | — |
| 609 | Bethesda | Maryland | — | — |
| 615 | Chesterfield | Missouri | — | — |
| 607 | New York | New York | — | — |
| 620 | Columbus | Ohio | — | — |
| 608 | Charleston | South Carolina | — | — |
| 601 | Nashville | Tennessee | — | — |
| 612 | Dallas | Texas | — | — |
| 610 | Norfolk | Virginia | — | — |
| 623 | Renton | Washington | — | — |
| 624 | Madison | Wisconsin | — | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT01118962, 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 16, 2018 · Synced Jul 22, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT01118962 live on ClinicalTrials.gov.