Exploratory Study to Assess the Effect of Fampridine (BIIB041) on Walking Ability and Balance in Participants With Multiple Sclerosis.

PHASE2CompletedINTERVENTIONAL
Enrollment

132

Participants

Timeline

Start Date

August 31, 2012

Primary Completion Date

August 31, 2013

Study Completion Date

August 31, 2013

Conditions
Multiple Sclerosis
Interventions
DRUG

BIIB041 (PR Fampridine)

10 mg twice daily, given orally. Doses of study treatment must be spaced at least 12 hours apart. If a dose of study treatment is delayed or missed, the participant should not dose again until their next scheduled dose. Tablets must be swallowed whole and should be taken without food.

OTHER

Placebo

Twice daily, given orally. Doses of study treatment must be spaced at least 12 hours apart. If a dose of study treatment is delayed or missed, the participant should not dose again until their next scheduled dose. Tablets must be swallowed whole and should be taken without food.

Trial Locations (23)

Unknown

Research Site, Ath

Research Site, Bruges

Research Site, Brussels

Research Site, Leuven

Research Site, Yvoir

Research Site, Halifax

Research Site, London

Research Site, Gatineau

Research Site, Greenfield Park

Research Site, Montreal

Research Site, Ancona

Research Site, Brescia

Research Site, Empoli

Research Site, Palermo

Research Site, Roma

Research Site, Breda

Research Site, Sittard-Geleen

Research Site, Gothenburg

Research Site, Stockholm

Research Site, Edgbaston

Research Site, Poole

Research Site, Swansea

Research Site, London

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Biogen

INDUSTRY

NCT01597297 - Exploratory Study to Assess the Effect of Fampridine (BIIB041) on Walking Ability and Balance in Participants With Multiple Sclerosis. | Biotech Hunter | Biotech Hunter