FDA Approves Belantamab Mafodotin-blmf for R/R Multiple Myeloma

On August 6, 2020, GlaxoSmithKline announced the U.S. Food and Drug Administration (FDA) has approved Blenrep (belantamab mafodotin-blmf) as a monotherapy treatment for adult patients with relapsed or refractory (R/R) multiple myeloma who have received at least four prior therapies including an anti-CD38 monoclonal antibody, a proteasome inhibitor and an immunomodulatory agent.

Read the corporate press release.

Read the FDA announcement.

Posted 8/6/2020