Open-label Study to Evaluate the Safety and Tolerability of iv Lacosamide in Japanese Adults With Partial-onset Seizures

PHASE3CompletedINTERVENTIONAL
Enrollment

9

Participants

Timeline

Start Date

June 30, 2014

Primary Completion Date

October 31, 2014

Study Completion Date

December 31, 2014

Conditions
EpilepsyPartial-onset Seizures
Interventions
DRUG

Lacosamide (200 mg/20 mL)

"Active Substance: Lacosamide~Pharmaceutical form: Solution for intravenous (iv) infusion~Concentration: adapted on concentration of oral dose in EP0009~Route of Administration: Drip infusion"

Trial Locations (5)

Unknown

81027, Hamamatsu

81024, Kodaira

81025, Sapporo

81003, Shizuoka

81023, Suita

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Parexel

INDUSTRY

lead

UCB Japan Co. Ltd.

INDUSTRY