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Completed Phase 2 Interventional Results available

To Determine Tolerability and Efficacy of Long-term Oral Lacosamide in Patients With Partial Seizures

ClinicalTrials.gov ID: NCT00552305

Public ClinicalTrials.gov record NCT00552305. 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 Jul 23, 2026, 1:34 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 Extension Trial to Determine Tolerability and Efficacy of Long-term Oral SPM 927 as Adjunctive Therapy in Patients With Partial Seizures

Study identification

NCT ID
NCT00552305
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
UCB Pharma
Industry
Enrollment
370 participants

Conditions and interventions

Interventions

  • lacosamide Drug

Drug

Eligibility (public fields only)

Age range
Not listed
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, 2001
Primary completion
Jan 31, 2010
Completion
Jan 31, 2010
Last update posted
Jul 16, 2018

2001 – 2010

United States locations

U.S. sites
43
U.S. states
26
U.S. cities
43
Facility City State ZIP Site status
Not listed Birmingham Alabama
Not listed Huntsville Alabama
Not listed Phoenix Arizona
Not listed Tucson Arizona
Not listed Little Rock Arkansas
Not listed Los Angeles California
Not listed Englewood Colorado
Not listed Gainesville Florida
Not listed Hollywood Florida
Not listed Miami Florida
Not listed Ponte Vedra Beach Florida
Not listed Chicago Illinois
Not listed Springfield Illinois
Not listed Indianapolis Indiana
Not listed Iowa City Iowa
Not listed Wichita Kansas
Not listed Crestview Hills Kentucky
Not listed Lexington Kentucky
Not listed Baltimore Maryland
Not listed Frederick Maryland
Not listed Boston Massachusetts
Not listed Ann Arbor Michigan
Not listed Detroit Michigan
Not listed Saint Paul Minnesota
Not listed Chesterfield Missouri
Not listed St Louis Missouri
Not listed Somerset New Jersey
Not listed New York New York
Not listed Durham North Carolina
Not listed Cincinnati Ohio
Not listed Cleveland Ohio
Not listed Columbus Ohio
Not listed Hershey Pennsylvania
Not listed Philadelphia Pennsylvania
Not listed Nashville Tennessee
Not listed Dallas Texas
Not listed Irving Texas
Not listed Lubbock Texas
Not listed Wichita Falls Texas
Not listed Bennington Vermont
Not listed Charlottesville Virginia
Not listed Marshfield Wisconsin
Not listed Milwaukee 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 16 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00552305, 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 23, 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 protocol, eligibility criteria, and contact information for NCT00552305 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →