BOSTON--(BUSINESS WIRE)--May 2, 2007 - Acorda Therapeutics, Inc.(R)
(Nasdaq: ACOR) today presented data from a Phase 3 clinical trial
of Fampridine-SR in people with multiple sclerosis (MS) at the
American Academy of Neurology meeting. Andrew Goodman, M.D.,
Director of the Multiple Sclerosis Center at the University of
Rochester, presented top-line results on walking ability, leg
strength, spasticity and clinician and subject global impressions.
Dr. Goodman also presented a review of safety data.
Presentation Highlights
The prospectively-designed analysis plan for the study was based
on a responder criterion, defined as a consistent improvement in
walking speed, as measured with the Timed 25 Foot Walk. A
significantly greater proportion of people taking Fampridine-SR
were Timed Walk Responders compared to people taking placebo (34.8
percent vs. 8.3 percent, p less than 0.0001). Increased response
rate with treatment was seen across all four major (relapsing and
progressive) types of MS.
The mean increase in walking speed, compared to pre-treatment,
for Fampridine-SR treated Timed Walk Responders was significantly
greater at every visit during the treatment period, compared to
both Fampridine-SR Timed Walk Non-Responders and placebo treated
patients (p less than 0.0001). The average increase in walking
speed over the treatment period, compared to baseline, was 25.2
percent for the drug treated Timed Walk Responders vs. 4.7 percent
for the placebo group. In follow-up visits, at two and four weeks
after the end of the treatment period, Responder and Non-responder
groups returned to their baseline walking speeds.
The clinical significance of the consistent response on the
timed walk was validated in the trial primarily by the 12-Item
Multiple Sclerosis Walking Scale (MSWS-12), a patient
self-assessment of walking disability. There was a statistically
significant improvement in the MSWS-12 score
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