Having withdrawn Blenrep (belantamab mafodotin-blmf) from the US market in 2022 after failing to confirm the benefit of the antibody-drug conjugate in late-line multiple myeloma, GSK plc is preparing to refile this year for use in the second-line setting based on the DREAMM-8 trial presented 2 June at the American Society of Clinical Oncology annual meeting. The company is confident that the DREAMM-7 and 8 trials together show a “consistency of treatment effect.”
Blenrep originally received accelerated approval from the US Food and Drug Administration in 2020 for patients with relapsed/refractory multiple myeloma...








