Takeda files for brentuximab vedotin approval in Japan; sanctioned by JPMA

22 March 2013

Japan’s largest drugmaker, Takeda Pharmaceutical (TYO: 4502) and its oncology subsidiary Millennium have submitted a new drug application to Japan’s Ministry of Health, Labor and Welfare (MHLW) for brentuximab vedotin for the treatment of adult patients with relapsed or refractory CD30 positive Hodgkin lymphoma (HL) and relapsed or refractory CD30 positive anaplastic large cell lymphoma (ALCL).

Seattle Genetics (Nasdaq: SGEN) and Millennium are jointly developing brentuximab vedotin, which the former already markets in the USA and has recently gained approval in Canada (the two territories for which it has commercialization rights) under the trade name Adcetris.

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