Seattle Genetics' Adcetris Gets EC Nod For Label Expansion

 | Feb 12, 2019 05:30AM ET

Seattle Genetics, Inc. (NASDAQ:SGEN) announced that its Japanese partner, Takeda Pharmaceutical Company Limited received approval from the European Commission (EC) to extend the marketing authorization for Adcetris (brentuximab vedotin) to include the combination of the drug and AVD (Adriamycin, vinblastine and dacarbazine) for the treatment of adult patients with previously untreated CD30+ stage IV classical Hodgkin lymphoma (HL).

As a result, Seattle Genetics will receive a milestone payment of $30 million from Takeda. Adcetris in combination with AVD is also approved in the United States for treatment of adult patients with previously untreated stage III or IV classical HL.

The approval was supported by positive results from the ECHELON-1 phase III study.

Seattle Genetics’ shares have returned 27.2% in the past year, against the industry ’s decline of 16.2%.