Open-Label Extension Study to Evaluate the Safety, Tolerability and Activity of Oral Fampridine-SR in Patients With Multiple Sclerosis

PHASE3CompletedINTERVENTIONAL
Enrollment

177

Participants

Timeline

Start Date

November 30, 2003

Primary Completion Date

January 31, 2011

Study Completion Date

April 30, 2011

Conditions
Multiple Sclerosis
Interventions
DRUG

Fampridine-SR b.i.d. (Twice Daily)

Dosage form - tablets.

Trial Locations (22)

10029

Corinne Goldsmith Dickinson Center for MS, New York

11219

Maimonides MS Care Center, Brooklyn

11794

SUNY Stony Brook, Stony Brook

14642

University of Rochester, Rochester

19107

Thomas Jefferson University Physicians, Philadelphia

21201

Maryland Center for MS, Baltimore

28207

CMC - Neuroscience & Spine Institute, Division of Neurology, Charlotte

30309

Shepherd Center, Atlanta

43221

Ohio State University MS Center, Columbus

44195

Cleveland Clinic Foundation, Cleveland

55422

The Schapiro Center for MS, Golden Valley

60637

University of Chicago, Chicago

63110

Washington University School of Medicine, Div. of Rehab/Neurology, St Louis

77030

University of Texas-Houston, Houston

85013

Barrow Neurology Clinic, St. Joseph's Hospital and Medical Center, Phoenix

87131

University of Mexico, MIND Imaging Center, Albuquerque

90033

USC, Keck School of Medicine Health Care Consultation Center, Los Angeles

97239

Oregon Health & Science University, MS Center of Oregon, UHS-42, Portland

98034

MS Center at Evergreen, Kirkland

07666

Gimbel MS Center at Holy Name Hospital, Teaneck

T2N 2T9

Foothills Medical Center, Calgary

M5B 1WB

St. Michael's Hospital, Toronto

Sponsors
All Listed Sponsors
lead

Acorda Therapeutics

INDUSTRY

NCT00654927 - Open-Label Extension Study to Evaluate the Safety, Tolerability and Activity of Oral Fampridine-SR in Patients With Multiple Sclerosis | Biotech Hunter | Biotech Hunter