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Stock impact report

Blenrep approved by US FDA for use in treatment of relapsed/refractory multiple myeloma

GlaxoSmithKline PLC (GSK) 
US:NYSE Investor Relations: gsk.com/en-gb/investors
Company Research Source: Business Wire
Significant unmet need for patients requires new and novel treatments1DREAMM-7 showed a 51% reduction in the risk of death and tripled median progression-free survival in 3L+ indicated population versus a daratumumab-based triplet2Blenrep is the only anti-BCMA accessible in the community setting where 70% of patients receive care, and with a new streamlined REMS program3Robust clinical development is ongoing to advance Blenrep in earlier lines of treatment, including newly diagnosed patients4  PHILADELPHIA--(BUSINESS WIRE)--GSK plc (LSE/NYSE: GSK) today announced the US Food and Drug Administration (FDA) has approved Blenrep (belantamab mafodotin-blmf) in combination with bortezomib and dexamethasone (BVd) for the treatment of adult patients with relapsed or refractory multiple myeloma who have received at least two prior lines of therapy, including a proteasome inhibitor (PI) and an immunomodulatory (IMID) agent.The Blenrep approval is supported by data from the pivotal DREAMM-7 p Show less Read more
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