European Commission approves Seagen’s Tukysa (tucatinib) for the treatment of patients with locally advanced or metastatic HER2 positive breast cancer

Seattle Genetics (Seagen)

12 February 2021 - Approved for adult patients with HER2 positive metastatic breast cancer who have received at least two prior anti-HER2 treatment regimens.

Seagen today announced that the European Commission has granted marketing authorization for Tukysa (tucatinib) in combination with trastuzumab and capecitabine for the treatment of adult patients with HER2-positive locally advanced or metastatic breast cancer who have received at least two prior anti-HER2 treatment regimens.

Read Seagen press release

Michael Wonder

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Michael Wonder

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Cancer , Outcome , Medicine , Europe