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B-Cell Depletion with Rituximab in Relapsing–Remitting Multiple Sclerosis
B-Cell Depletion with Rituximab in Relapsing–Remitting Multiple Sclerosis
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B-Cell Depletion with Rituximab in Relapsing–Remitting Multiple Sclerosis
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B-Cell Depletion with Rituximab in Relapsing–Remitting Multiple Sclerosis
B-Cell Depletion with Rituximab in Relapsing–Remitting Multiple Sclerosis

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B-Cell Depletion with Rituximab in Relapsing–Remitting Multiple Sclerosis
B-Cell Depletion with Rituximab in Relapsing–Remitting Multiple Sclerosis
Journal Article

B-Cell Depletion with Rituximab in Relapsing–Remitting Multiple Sclerosis

2008
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Overview
In this phase 2 trial involving 104 patients with relapsing–remitting multiple sclerosis, patients who received rituximab on days 1 and 15 had fewer gadolinium-enhancing lesions on magnetic resonance imaging and fewer relapses during 48 weeks of follow-up than patients who received placebo. Rituximab was associated with more adverse events within 24 hours after the first infusion. The study was too small and short to assess uncommon adverse events or long-term safety. Patients with relapsing–remitting multiple sclerosis who received rituximab on days 1 and 15 had fewer gadolinium-enhancing lesions on MRI and fewer relapses during 48 weeks of follow-up than patients who received placebo. Multiple sclerosis, the prototypical inflammatory demyelinating disease of the central nervous system, is second only to trauma as a cause of acquired neurologic disability in young adults. 1 Multiple sclerosis usually begins as a relapsing, episodic disorder (relapsing–remitting multiple sclerosis), evolving into a chronic neurodegenerative condition characterized by progressive neurologic disability. 2 The traditional view of the pathophysiology of multiple sclerosis has held that inflammation is principally mediated by CD4+ type 1 helper T cells. Therapies (e.g., interferon beta and glatiramer acetate) developed on the basis of this theory decrease the relapse rate by approximately one third 3 , 4 but do not fully . . .