FDA Approves Genentech’s Rituxan For Rare Autoimmune Disease Pemphigus Vulgaris

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via Genentech, announced on 6/8/2018 that the U.S. Food and Drug Administration (FDA) has approved Rituxan (rituximab) for the treatment of adults with moderate to severe pemphigus vulgaris (PV), a rare, serious, potentially life-threatening condition characterized by progressive painful blistering of the skin and mucous membranes.

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