108
Participants
Start Date
June 30, 2012
Primary Completion Date
May 31, 2014
Study Completion Date
May 31, 2014
Fampridine-SR
Subjects will all receive Fampridine-SR in an open label enrichment phase lasting four weeks. Those 40% improvin the most measured by SSST will go onto the intervention. Here randomization in a 1:1 key between Fampridine-SR and placebo will be undertaken. Treatment will be of either Fampridine-SR 10 mg BID or placebo BID for four weeks. Arms will be double blind.
Odense University Hospital, Odense
Sønderborg Hospital, Sønderborg
Esbjerg Hospital, Esbjerg
Vejle Hospital, Vejle
Collaborators (1)
Region of Southern Denmark
OTHER
Biogen
INDUSTRY
University of Southern Denmark
OTHER