The European Medicines Agency will this week again consider whether to recommend pan-EU marketing approval for belantamab mafodotin, GlaxoSmithKline’s novel multiple myeloma treatment that last week overcame ocular toxicity concerns to score a US Food and Drug Administration panel endorsement.
The antibody-drug conjugate, for relapsed or refractory multiple myeloma, is among a number of new drugs that are up for...








