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Idec Zevalin

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Executive Summary

FDA's Oncologic Drugs Advisory Committee will review Zevalin (ibritumomab tiuxetan) on Sept. 11 for treatment of relapsed or refractory low-grade, follicular, CD20+ transformed, B-cell non-Hodgkin's lymphoma and rituximab-refractory follicular NHL. Meeting will begin at 8 a.m. at the Holiday Inn in Bethesda, Md

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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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