Takeda wins new EC approval for Adcetris

4 June 2025

The European Commission (EC) has approved Adcetris (brentuximab vedotin) in combination with etoposide, cyclophosphamide, doxorubicin, dacarbazine and dexamethasone (ECADD) – a chemotherapy regimen – in adult patients with newly diagnosed Stage IIb with risk factors/III/IV Hodgkin lymphoma.

The decision follows a positive opinion from the Committee for Medicinal Products for Human Use (CHMP) on April 25, 2025, said Japan’s Takeda (TYO: 4502).

The drug, which Takeda licensed for Pfizer (NYSE: PFE) for certain territories including Europe, generated sales of $895 million in the last fiscal year, up 18% year-on-year, for the Japanese firm.

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