GSK/Corixa Bexxar NDA
Executive Summary
Corixa/GlaxoSmithKline's Bexxar (tositumomab) could receive review for treatment of low-grade or transformed low-grade non-Hodgkin's lymphoma by FDA's Oncologic Drugs Advisory Committee at the tentatively scheduled Sept. 23-24 meeting. Corixa requested committee review of the drug in its appeal of a March 12 "complete review" letter (1"The Pink Sheet" May 20, In Brief)...
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Corixa expects to present Bexxar (tositumomab) to FDA's Oncologic Drug Advisory Committee before the end of the year. The committee has cancelled its Sept. 23 meeting date, but is tentatively scheduled to reconvene Dec. 17 and 18. Corixa requested the review in its appeal of a March 12 "complete review" letter for the non-Hodgkin's lymphoma therapy (1"The Pink Sheet" July 1, In Brief)...
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