annual relapse rate prior to entry,
versus patients who received the 20 mg dose (62 percent reduction).
The time to the first relapse was significantly delayed from 80
days in the 20 mg group to 213 days in the 40 mg group (p =
0.0367). The overall safety profile was similar to that of the 20
mg dose. Some features of injection site reactions and immediate
post-injection reactions were more common.
About Multiple Sclerosis
Multiple Sclerosis (MS) is the leading cause of neurological
disability in young adults. It is estimated that 400,000 people in
the United States are affected by this disease, and that over two
million people are affected worldwide. MS is a progressive,
demyelinating disease of the central nervous system affecting the
brain, spinal cord and optic nerves.
Patients with MS may experience physical symptoms and/or
cognitive impairments, including weakness, fatigue, ataxia,
physical dysfunction, bladder and bowel problems, sensory effects,
and visual impairment. MS also has a significant impact on the
sufferers' social functioning and overall quality of life.
About COPAXONE(R)
COPAXONE(R) is indicated for the reduction of the frequency of
relapses in RRMS. The most common side effects of COPAXONE(R) are
redness, pain, swelling, itching, a lump or an indentation at the
site of injection, weakness, infection, pain, nausea, joint pain,
anxiety, and muscle stiffness.
COPAXONE(R) is now approved in 47 countries worldwide, including
the United States, Canada, Mexico, Australia, Israel, and all
European countries. In North America, COPAXONE(R) is marketed by
Teva Neuroscience, Inc., which is a subsidiary of Teva
Pharmaceutical Industries Ltd. (NASDAQ:TEVA). In Europe,
COPAXONE(R) is marketed by Teva Pharmaceutical Industries Ltd. and
sanofi-aventis. COPAXONE(R) is a registered trademark of Teva
Pharmaceutical Industries Ltd.
Teva Pharmaceutical Industries Ltd., headquartered in Israel, is
among the top 20 phar
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