Open Label Extension Study to Evaluate the Safety and Tolerability of Oral Fampridine-Sustained Release (SR) in Canadian Participants With Multiple Sclerosis Who Participated in Acorda Extension Trials.

PHASE3CompletedINTERVENTIONAL
Enrollment

38

Participants

Timeline

Start Date

December 31, 2010

Primary Completion Date

June 30, 2012

Study Completion Date

June 30, 2012

Conditions
Multiple Sclerosis
Interventions
DRUG

BIIB041 (Fampridine-SR)

10 mg twice a day (BID) sustained-release (SR) tablets by mouth for up to 27 months (in addition to treatment in previous studies) or until the product is commercially available, whichever comes first. Doses of study treatment must be spaced at least 12 hours apart.

Trial Locations (5)

Unknown

Foothills Medical Center, Calgary

University of British Columbia, Vancouver

River Valley Health, Fredericton

QEII Health Sciences Centre, Halifax

Ottawa Hospital General Campus, Ottawa

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Acorda Therapeutics

INDUSTRY

lead

Biogen

INDUSTRY