Copaxone Approved In Switzerland For Relapse-Remitting Multiple Sclerosis
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Copaxone Approved In Switzerland For Relapse-Remitting Multiple Sclerosis

JERUSALEM, ISRAEL -- May 11, 1999-The Swiss Intercantonal Medicines Control office has approved Hoechst Roussel Schweiz’s Copaxone(R) (glatiramer acetate for injection) for the treatment of relapsing-remitting multiple sclerosis (RRMS), marking Copaxone’s first Western European approval.

The approved multiple sclerosis therapeutic indication is for the reduction of frequency of relapses and decreasing the progression of disability. Copaxone is the only MS-specific immunomodulator available today.

There are approximately 3,500 people with RRMS in Switzerland, of whom only less than one-third are currently being treated. People who suffer from relapsing remitting MS experience relapses - episodes of impaired vision, movement disorders -- followed by remission. These symptoms are caused by attacks on the myelin sheath, the covering which surrounds nerve fibres.

The most commonly-observed adverse reactions associated with the use of Copaxone are injection site reactions, flushing and chest pain. Approximately 10 percent of patients exposed to the drug in pre-marketing studies experienced a constellation of symptoms that could include flushing, chest pain, palpitations, anxiety, dyspnea, constriction of the throat and urticaria. These symptoms were invariably transient and self-limited.

The cause of MS is unknown and usually strikes people between the ages of 20 and 40. Seventy-three per cent of MS patients are women.

Related Links: Copaxone, Hoechst Roussel Schweiz

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