Trials / Completed
CompletedNCT00440518
A Study Designed to Test the Effectiveness and Safety of Treating Patients With Lacosamide for Migraine Prophylaxis
A Multicenter, Randomized, Double-blind, Placebo-controlled Trial to Assess the Efficacy and Safety of 100mg/Day and 300mg/Day Lacosamide for Migraine Prophylaxis.
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 218 (actual)
- Sponsor
- UCB Pharma · Industry
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to see how safe and effective Lacosamide (LCM) is when taken by mouth, twice a day for up to 18 weeks to prevent migraines.
Detailed description
This study is for subjects who have been diagnosed with migraine for at least one year and who are currently taking an effective abortive medication(s).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Lacosamide | Lacosamide 100mg immediate-release film-coated tablet (white,oval) oral administration twice daily 12 hours apart |
| OTHER | Placebo | Immediate-release film coated tablet (white, oval), oral administration twice daily 12 hours apart |
| DRUG | Lacosamide | Lacosamide 300mg, immediate-release film coated tablet (white,oval), oral administration twice daily 12 hours apart. |
Timeline
- Start date
- 2007-02-01
- Primary completion
- 2008-07-01
- Completion
- 2008-07-01
- First posted
- 2007-02-27
- Last updated
- 2018-07-17
- Results posted
- 2009-09-11
Locations
24 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00440518. Inclusion in this directory is not an endorsement.