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

Completed · Phase 2

Conditions studied: Partial Epilepsies

In brief

The purpose of this trial is to determine whether lacosamide is safe and effective for long-term use in patients with partial-seizures from epilepsy.

Key facts

Study ID

NCT00552305

Run by

UCB Pharma

People needed

370

Starts

2001-08-01

Expected to finish

2010-02-01

Last updated by the study team

2018-07-17

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Completion of parent clinical trial for treatment of partial seizures.

You may not qualify if…

• Receiving any study drug or experimental device other than lacosamide.
• Meets withdrawal criteria for parent trial or experiencing ongoing serious adverse event.

Where it is running

• Study site — Huntsville, Alabama, United States
• Study site — Phoenix, Arizona, United States
• Study site — Tucson, Arizona, United States
• Study site — Little Rock, Arkansas, United States
• Study site — Los Angeles, California, United States
• Study site — Englewood, Colorado, United States
• Study site — Gainesville, Florida, United States
• Study site — Hollywood, Florida, United States
• Study site — Miami, Florida, United States
• Study site — Ponte Vedra Beach, Florida, United States
• Study site — Chicago, Illinois, United States
• Study site — Springfield, Illinois, United States
• Study site — Indianapolis, Indiana, United States
• Study site — Iowa City, Iowa, United States
• Study site — Wichita, Kansas, United States
• Study site — Crestview Hills, Kentucky, United States
• Study site — Lexington, Kentucky, United States
• Study site — Baltimore, Maryland, United States
• Study site — Frederick, Maryland, United States
• Study site — Boston, Massachusetts, United States
• Study site — Ann Arbor, Michigan, United States
• Study site — Detroit, Michigan, United States
• Study site — Saint Paul, Minnesota, United States
• Study site — Chesterfield, Missouri, United States
• Study site — Birmingham, Alabama, United States

Full record on ClinicalTrials.gov

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