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Unmet Need in Multiple MyelomaMode of ActionAboutReimbursement InformationStudy OverviewStudy Design and Baseline DemographicsEfficacy OutcomesFollow-up Analyses OutcomesSafety ProfileMagnetisMM-3 StudySafetyDosingMaterialsVideosEventsSupport & Resources

The content of this website has been produced in line with the ELREXFIO®▼ (elranatamab) Summary of Product Characteristics for Great Britain and Northern Ireland. For ELREXFIO®▼ (elranatamab) Prescribing Information for Great Britain and Northern Ireland click here.

NICE Final Guidance

Elrexfio® (elranatamab) is recommended by the National Institute for Health and Care Excellence (NICE) within managed access as an option for treating relapsed and refractory multiple myeloma in adults, only after 3 or more lines of treatment (including an immunomodulatory drug, a proteasome inhibitor and an anti-CD38 antibody) when the multiple myeloma has progressed on the last treatment. It is only recommended if the conditions in the managed access agreement for elranatamab are followed.

Click here to read the NICE Final Guidance for Elrexfio® in full on the NICE website.1

ELREXFIO® Support and Resources

Explore the resouces we have available to support you with the treatment of patients on ELREXFIO®

Explore Support and ResourcesLoading
ReferencesReferences:NICE: Final Guidance. Available at: https://www.nice.org.uk/guidance/ta1023
Mode of ActionELREXFIO® is a humanised BCMA-CD3-directed bispecific antibody Read moreLoadingELREXFIO® Safety ProfileSafety profile of ELREXFIO® in all patients treated at the recommended dose in the Phase 2 MagnetisMM-3 study (n=183) Read moreLoading
PP-L1A-GBR-0523. December 2024

Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search 

for MHRA Yellow Card in Google Play or Apple App Store

 

Adverse events should also be reported to Pfizer Medical Information on 01304 616161

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