EC approval for Zynlonta as large B-cell lymphoma therapy

21 December 2022

The European Commission (EC) has granted conditional marketing authorization for the use of Zynlonta (loncastuximab tesirine) for the treatment of relapsed or refractory diffuse large B-cell lymphoma (DLBCL), Swedish Orphan Biovitrum (STO: SOBI), also known as Sobi, and Switzerland’s ADC Therapeutics (NYSE: ADCT) announced today.

The Swiss firm’s shares were trading up 28% at $4.06 in pre-market US activity, while Sobi was barely changed by late morning.

The approval follows a positive opinion issued in September by the Committee for Medicinal Products for Human Use of the European Medicines Agency (EMA).

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