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![]() The larger label increases the drug's reach to 43,000 patients a year and will be used as part of a therapy for previously untreated follicular occurrences of the disease, which are the most common forms, according to the National Cancer Institute. It will be used in patients who achieve a partial or complete response to first-line chemotherapy – or the primary stage of treatment. The new addition coincides with the 2002 FDA approval of Zevalin as a treatment for patients with relapsed or refractory, low-grade or follicular B-cell Non-Hodgkin's lymphoma. NEXT PAGE >> Related headlines Orange's St. Joseph Hospital debuts revolutionary procedure 'OC METRO Minute,' Sept. 3: Visiogen set to be acquired by Abbot for $400 million O.C. Affiliate of Susan G. Komen for the Cure launches Race Registration Suite |
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