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Pfizer's ELREXFIO™ Receives U.S. FDA Accelerated Approval for Relapsed or Refractory Multiple Myeloma – India Education | Latest Education News | Global Educational News

Pfizer Inc. (NYSE:PFE) today announced the U.S. Food and Drug Administration (FDA) has granted accelerated approval to ELREXFIO™ (elranatamab-bcmm) for the treatment of adult patients with relapsed or refractory multiple myeloma (RRMM) who have recei ....

Angela Hwang , Ajay Nooka , Jenny Ahlstrom , Approval Program , Japanese Ministry Of Health , Pfizer Inc , Healthtree Foundation For Multiple Myeloma , European Hematology Association , Drug Administration , European Medicines Agency , Chief Commercial Officer , Global Biopharmaceuticals Business , Hematology Association , Multiple Myeloma Program , Winship Cancer Institute , Boxed Warning , Mitigation Strategy , Chief Executive Officer , Healthtree Foundation , Patient Access Navigators , Pfizer Oncology Together , Breakthrough Therapy Designation , Orphan Drug Designations , Project Orbis , Japanese Ministry ,

FDA Approves Elranatamab for Relapsed or Refractory Multiple Myeloma

The FDA has granted accelerated approval to elranatamab-bcmm (Elrexfio) for the treatment of adult patients with relapsed or refractory multiple myeloma who have previously received at least 4 lines of therapy, including a proteasome inhibitor, an immunomodulatory agent, and an anti-CD38 monoclonal antibody. ....

Angela Hwang , Ajay Nooka , International Myeloma Working Group , Global Biopharmaceuticals Business , Multiple Myeloma Program , Winship Cancer Institute , Emory University , Multiple Myeloma , Fda Approval ,

FDA Grants Accelerated Approval to Elranatamab-bcmm for Relapsed or Refractory Multiple Myeloma

Elranatamab-bcmm (Elrexfio; Pfizer) is a BCMA-CD3-targeted bispecific antibody approved for adults with relapsed or refractory multiple myeloma who were previously administered at least 4 lines of therapy that included a proteasome inhibitor, an immunomodulatory agent, and an anti-CD38 monoclonal antibody. ....

United States , Angela Hwang , Ajay Nooka , American Society Of Hematology Annual Meeting , Breakthrough Therapy Designation , Priority Review , Global Biopharmaceuticals Business , American Society , Hematology Annual Meeting , Multiple Myeloma Program , Winship Cancer Institute , Emory University ,

New Bispecific Antibody Nabs Conditional FDA Approval for Myeloma

Elranatamab produced 58% response rate as fifth-line therapy ....

Ajay Nooka , Charles Bankhead , Winship Cancer Institute , Emory University , Medpage Today ,

Pfizer's ELREXFIO™ Receives U.S. FDA Accelerated Approval for Relapsed or Refractory Multiple Myeloma

The approval of ELREXFIO is based on clinically meaningful response rates and duration of response from Phase 2 MagnetisMM-3 study

ELREXFIO is the first off-the-shelf fixed-dose subcutaneous.
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