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
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Pink Sheet for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?