Phase I DREAMM-9 Study of Belantamab Mafodotin + VRd in ASCT-Ineligible Newly Diagnosed MM

December 11-14, 2021; Atlanta, Georgia
The safety profile of belantamab mafodotin plus VRd for patients with newly diagnosed MM who are not eligible for ASCT was similar to the known safety of single-agent belantamab mafodotin in patients with R/R MM.
Format: Microsoft PowerPoint (.ppt)
File Size: 497 KB
Released: December 16, 2021

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