Yescarta approved in Europe for specific lymphomas

28 August 2018

The European Commission has granted marketing authorization for Yescarta (axicabtagene ciloleucel) as a treatment for adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) and primary mediastinal large B-cell lymphoma (PMBCL), after two or more lines of systemic therapy.

The drug was originated by US biotech Kite Pharma, which was acquired by US biotech major Gilead Sciences (Nasdaq: GILD) in an $11.9 billion deal in August 2017. Gilead’s shares were up 1.62% at $74.78 in mid-morning trading on Monday.

Axicabtagene ciloleucel was approved by the US Food and Drug Administration on October 18, 2017, and in the second quarter of this year generating sales of $68 million for Gilead.

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