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October 31, 2012
07:09 EDTSGENSeattle Genetics' Adcetris receives European Commission marketing authorization
Seattle Genetics' collaborator, Millennium: The Takeda Oncology Company, a wholly owned subsidiary of Takeda Pharmaceutical, announced that the European Commission has granted conditional marketing authorization for Adcetris (brentuximab vedotin). Adcetris was approved for two indications: (1) the treatment of adult patients with relapsed or refractory CD30-positive Hodgkin lymphoma following autologous stem cell transplant or following at least two prior therapies when ASCT or multi-agent chemotherapy is not a treatment option, and (2) for the treatment of adult patients with relapsed or refractory systemic anaplastic large cell lymphoma. As a result, under the collaboration Seattle Genetics will receive two milestone payments from Millennium, one for each indication, totaling $25M. ADCETRIS is an antibody-drug conjugate directed to CD30.
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May 14, 2013
09:04 EDTSGENSeattle Genetics announces ADCETRIS supplemental filing accepted by FDA
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May 7, 2013
16:22 EDTSGENSeattle Genetics reports Q1 EPS (14c), consensus (20c)
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