FDA accepts Seattle Genetics' lymphoma drug Adcetris for review

05/16/2013 | Bloomberg Businessweek · PharmaTimes (U.K.)

The FDA has accepted Seattle Genetics' supplemental biologics license application for the use of Adcetris, or brentuximab vedotin, for retreatment and use beyond 16 cycles of therapy in patients with relapsed Hodgkin lymphoma and systemic anaplastic large cell lymphoma. A decision is expected by Sept. 14.

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Bloomberg Businessweek · PharmaTimes (U.K.)

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