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

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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.

Released: December 16, 2021

Expiration: December 15, 2022

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Supported by educational grants from

AbbVie

AstraZeneca

Daiichi Sankyo, Inc.

GlaxoSmithKline

Incyte Corporation

Jazz Pharmaceuticals, Inc.

Merck Sharp & Dohme Corp.

Novartis Pharmaceuticals Corporation