FAME - Fampyra Outcome Measures Study: a Study of Different Outcome Measures on the Effect of Fampyra

PHASE4CompletedINTERVENTIONAL
Enrollment

108

Participants

Timeline

Start Date

June 30, 2012

Primary Completion Date

May 31, 2014

Study Completion Date

May 31, 2014

Conditions
Multiple Sclerosis
Interventions
DRUG

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.

Trial Locations (4)

5000

Odense University Hospital, Odense

6400

Sønderborg Hospital, Sønderborg

6700

Esbjerg Hospital, Esbjerg

7100

Vejle Hospital, Vejle

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Region of Southern Denmark

OTHER

collaborator

Biogen

INDUSTRY

lead

University of Southern Denmark

OTHER