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Safety and Efficacy study of Oral Fampridine-SR on Walking Ability in Multiple Sclerosis - Article


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Clinical Trial: Safety and Efficacy study of Oral Fampridine-SR on Walking Ability in Multiple Sclerosis

This study has been completed.

Sponsored by: Acorda Therapeutics
Information provided by: Acorda Therapeutics

Purpose

Multiple Sclerosis (MS) is a disorder of the body's immune system that affects the Central Nervous System (CNS). Normally, nerve fibers carry electrical impulses through the spinal cord, providing communication between the brain and the arms and legs. In people with MS, the fatty sheath that surrounds and insulates the nerve fibers (called "myelin") deteriorates, causing nerve impulses to be slowed or stopped. As a result patients with MS may experience periods of muscle weakness and other symptoms such as numbness, loss of vision, loss of coordination, paralysis, spasticity, mental and physical fatigue and a decrease in the ability to think and/or remember. These periods of illness may come (exacerbations) and go (remissions). Fampridine-SR is an experimental drug that increases the ability of the nerve to conduct electrical impulses. This study will evaluate the effects of Fampridine-SR on the walking ability of subjects with MS, as well as to examine the effects on muscle strength and spasticity. The study will also examine the possible risks of taking Fampridine-SR.

Condition Treatment or Intervention Phase
Multiple Sclerosis
 Drug: Fampridine-SR (4-aminopyridine, 4-AP)
Phase II

MedlinePlus related topics:  Multiple Sclerosis

Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study

Official Title: Double-Blind, Placebo-Controlled, 20-Week, Parallel Group Study to Evaluate Safety, Tolerability and Activity of Oral Fampridine-SR in Subjects with Multiple Sclerosis

Further Study Details: 

Expected Total Enrollment:  180

Study start: February 2003;  Study completion: December 2003

Eligibility

Ages Eligible for Study:  18 Years   -   70 Years,  Genders Eligible for Study:  Both

Criteria

INCLUSION CRITERIA:

  • Have a confirmed diagnosis of Multiple Sclerosis
  • Are able to walk with or without an assisted device

EXCLUSION CRITERIA:

  • Pregnancy, breastfeeding or females of childbearing potential not using adequate birth control
  • Participating in other investigational drug trials
  • A medical history or clinical findings that preclude entry into the study
  • A medication history that precludes entry into the study
  • Previously treated with 4-aminopyridine (4-AP)

Location Information


Arizona
      Barrow Neurological Institute at St. Joseph Hospital and Medical Center, Phoenix,  Arizona,  85013,  United States

California
      USC School of Medicine, Los Angeles,  California,  90033,  United States

Connecticut
      Yale University MS Center, New Haven,  Connecticut,  06510,  United States

Georgia
      MS Center at Shepherd Center, Atlanta,  Georgia,  30309,  United States

Illinois
      University of Chicago, Chicago,  Illinois,  60637,  United States

Maryland
      University of Maryland at Baltimore, Baltimore,  Maryland,  21210,  United States

Minnesota
      Fairview MS Center, Minneapolis,  Minnesota,  55454,  United States

Missouri
      Washington University School of Medicine, St. Louis,  Missouri,  63110,  United States

New Jersey
      Gimbel MS Center, Teaneck,  New Jersey,  07666,  United States

New Mexico
      University of New Mexico, Albuquerque,  New Mexico,  87131,  United States

New York
      SUNY Stony Brook, Stony Brook,  New York,  11794,  United States

      Mt. Sinai School of Medicine - MS Center, New York,  New York,  10029,  United States

      Maimonides MS Care Center, Brooklyn,  New York,  11219,  United States

      University of Rochester Medical School, Rochester,  New York,  14642,  United States

North Carolina
      Carolinas Medical Center MS Clinic, Charlotte,  North Carolina,  28207,  United States

Ohio
      Cleveland Clinic Foundation, Cleveland,  Ohio,  44195,  United States

      Ohio State University, Columbus,  Ohio,  43210,  United States

Oregon
      Oregon Health Sciences University; MS Center, Portland,  Oregon,  97201,  United States

Pennsylvania
      Thomas Jefferson University, Philadelphia,  Pennsylvania,  19107,  United States

Texas
      University of Texas-Houston, Houston,  Texas,  77030,  United States

Washington
      University of Washington MS Clinical Center, Seattle,  Washington,  98195,  United States

      Swedish Medical MS Center, Seattle,  Washington,  98122,  United States

Wisconsin
      University of Wisconsin, Madison,  Wisconsin,  53792,  United States

Canada, Alberta
      University of Calgary and Foothills Hospital, Calgary,  Alberta,  T2N 2T9,  Canada

Canada, Ontario
      St. Michael's Hospital, Toronto,  Ontario,  M5B 1WB,  Canada

More Information

http://www.acorda.com

Study ID Numbers:  MS-F202
Record last reviewed:  January 2004
Last Updated:  October 13, 2004
Record first received:  January 29, 2003
ClinicalTrials.gov Identifier:  NCT00053417
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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