Johnson & Johnson announces European approval of Talvey in myeloma

Johnson & Johnson’s Janssen Pharmaceutical announced that the European Commission has granted conditional marketing authorization of Talvey as monotherapy for the treatment of adult patients with relapsed and refractory multiple myeloma who have received at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor, and an anti-CD38 antibody and have demonstrated disease progression on the last therapy. The EC approval follows the Food and Drug Administration approval of talquetamab for the treatment of adult patients with relapsed or refractory multiple myeloma who received at least four prior lines of therapy, including a proteasome inhibitor, an immunomodulatory agent, and an anti-CD38 antibody.