Blenrep receives FDA approval in relapsed or refractory multiple myeloma

Share on facebook
Share on twitter
Share on linkedin
Share on email
Share on print

Blenrep (belantamab mafodotin-blmf) has received FDA approval as a monotherapy treatment for adult patients with relapsed or refractory multiple myeloma who have received at least four prior therapies including an anti-CD38 monoclonal antibody, a proteasome inhibitor and an immunomodulatory agent.

To access this subscriber-only content please log in or subscribe.

If your institution has a site license, log in with IP-login or register for a sponsored account.*
*Not all site licenses are enrolled in sponsored accounts.

Login Subscribe
Table of Contents

YOU MAY BE INTERESTED IN

Login