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Genentech, Biogen Idec, and Roche File Supplemental Biologics License Application for Rituxan in Non-Hodgkin Lymphoma

Genentech, Inc. (DNA), Biogen Idec, Inc. (BIIB), and Roche (SWX) have completed the filing of a supplemental biologics license application (sBLA) with the U.S. Food and Drug Administration (FDA) for an additional indication of Rituxan (Rituximab) in previously untreated patients with intermediate-grade or aggressive, CD-20-positive, B-cell, non-Hodgkin lymphoma (NHL)