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On July 9, 2021, the U.S. Food and Drug Administration (FDA) approvedĀ daratumumab and hyaluronidase-fihj in combination with pomalidomide and dexamethasone for adult patients with multiple myeloma (MM) who have received at least one prior line of therapy including lenalidomide and a proteasome inhibitor.
Read the FDA announcement.
Read Janssen's announcement.
Posted 7/12/2021