
FDA approved Betaseron, the first of several biotech products that have had a major impact on multiple sclerosis treatment
On Jul. 23, 1993, the U.S. Food and Drug Administration (FDA) approved Betaseron, developed by Chiron and Berlex Laboratories, the first of several biotechnology products that have had a major impact on multiple sclerosis treatment.
Today, a Bayer company product, BETASERON® (interferon beta-1b) is a prescription medicine used to treat relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, in adults.
Five injectables – four beta interferons (Avonex, Betaseron, Extavia, and Rebif) and the copolymer polypeptide mixture glatiramer acetate – are generally viewed as first-line treatments for MS. Most experts recommend that treatment begin with one of these drugs as soon as the diagnosis of relapsing -remitting MS has been confirmed.
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Source: Multiple Sclerosis Association of America
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