17 August 2023 - Regeneron Pharmaceuticals today announced that the EMA has accepted for review the marketing authorisation application for odronextamab to treat adult patients with relapsed/refractory follicular lymphoma or relapsed/refractory diffuse large B-cell lymphoma, who have progressed after at least two prior systemic therapies.
The EMA previously granted odronextamab orphan drug designation for follicular lymphoma and diffuse large B-cell lymphoma.