Myeloma BCMA Therapy In Spotlight: EMA Considers Fast Tracking GSK Filing

EU Filing Understood To Be Expected in H1 2020

The European Medicines Agency is this week deciding whether GlaxoSmithKline’s planned EU marketing application for its BCMA-targeting therapy merits an accelerated assessment.

Running
GSK is leading the race to market a BCMA-targeting therapy for myeloma • Source: Shutterstock

GlaxoSmithKline should soon learn whether the European Medicines Agency will fast track its planned EU marketing application for belantamab mafodotin, one of several BCMA-targeting therapies being developed to treat multiple myeloma.

GSK’s request for accelerated assessment for the antibody-drug conjugate is due to be considered at this week's monthly meeting of the EMA’s drug evaluation committee, the CHMP, which is taking place on 11-14 November

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