300
Participants
Start Date
May 31, 2005
Primary Completion Date
June 30, 2006
Study Completion Date
September 30, 2006
Fampridine-SR
Tablets, 10 mg, twice daily, 14 weeks
Placebo
sugar pill, twice a day (b.i.d.)
Corinne Goldsmith Dickinson Center for MS, New York
Maimonides Medical Center, Brooklyn
SUNY - Stony Brook, Stony Brook
University of Rochester, Rochester
Allegheny General Hospital, Allegheny Neurological Associates, Pittsburgh
Thomas Jefferson University Physicians, Philadelphia
Maryland Center for MS, Baltimore
Carolinas Healthcare System, Charlotte
Shepard Center, Atlanta
University of Alabama, Birmingham
Ohio State University MS Center, Columbus
Cleveland Clinical Foundation, Cleveland
Indiana University MS Center, Indianapolis
Wayne State University, Department of Neurology, Detroit
The Schapiro Center for MS, Golden Valley
University of Chicago, Chicago
Washington University SOM, St Louis
University of Texas - Houston, Houston
University of Colorado Health Sciences Center, Denver
Barrow Neurology Clinic, St. Joseph's Hospital and Medical Center, Phoenix
University of Mexico, MIND Imaging Center, Albuquerque
USC, Keck School of Medicine, Los Angeles
UC Davis, Sacramento
Oregon Health & Science University, MS Center of Oregon, UHS-42, Portland
MS Hub Medical Group, Seattle
University of Washington, MS Research Center, Seattle
Multiple Sclerosis Treatment Center, Derby
Gimbel MS Center at Holy Name Hospital, Teaneck
Neurological Research Center, Inc., Bennington
Fletcher Allen Health Care, Burlington
Foothills Medical Center, Calgary
University of British Columbia, Vancouver Coastal Health Research Institute, Vancouver
QEII Health Sciences Centre, Nova Scotia Rehabilitation Centre Site, Halifax
Ottawa Hospital General Campus, Ottawa
Lead Sponsor
Acorda Therapeutics
INDUSTRY