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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