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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 Elrexfio® (elranatamab) Prescribing Information for United Kingdom click here.​

MagnetisMM-3 Study Design and Baseline Demographics

MagnetisMM-3 Study Design

MagnetisMM-3 (trial ongoing) is an open-label, global, multicentre, non-randomised Phase 2 study evaluating ELREXFIO® monotherapy in patients with relapsed or refractory multiple myeloma (RRMM), refractory to at least 1 proteasome inhibitor (PI), 1 immunomodulatory drug (IMiD), and 1 anti-CD38 monoclonal antibody.1

The primary endpoint is objective response rate (ORR) as assessed by blinded independent central review (BICR). Key secondary endpoints include: minimal residual disease (MRD) negativity rate (10-5), time to response (TTR), duration of response (DoR), progression-free survival (PFS), complete response rate (CRR), and safety.1

Adapted from ELREXFIO® Summary of Product Characteristics.1

*The dosing interval was changed from QW to Q2W in patients who achieved an IMWG response category of partial response or better with responses persisting for at least 2 months.1

Baseline Patient Characteristics:
Patients with no prior BCMA-directed therapy (Cohort A)

Patient demographics and key prognostic factors for MM1,2

  BCMA-directed therapy-naïve (n=123)
Median age (range), years 68.0 (36-89)
Male, n (%) 68 (55.3)
Female, n (%) 55 (44.7)
Race, n (%)
White
Asian
Hispanic/Latino
Black or African American
72 (58.5)
16 (13.0)
11 (8.9)
9 (7.3)
Extramedullary disease,* n(%) 39 (31.7)
High cytogenic risk,† n(%) 31 (25.2)
Revised International Staging System (R-ISS stage), n(%)
I
II
III
28 (22.8)
68 (55.3)
19 (15.4)
Median lines of prior therapy, n (range) 5 (2-22)
Triple-class refractory, n (%) 119 (96.7)
Refractory to last line of therapy, n (%) 118 (95.9)
Prior allogenic stem cell transplantation, n (%) 7 (5.7)
Prior autologous stem cell transplantation, n (%) 84 (68.3)

Adapted from ELREXFIO® Summary of Product Characteristics and Pfizer Data on File. REF-E1A2136.1

Please note that percentages may not total 100 due to rounding. 

*Defined as the presence of any plasmacytoma (extramedullary and/or paramedullary with a soft tissue component).1
†Includes the following chromosomal abnormalities: t(4;14), t(14;16), and del(17p).1

ReferencesBCMA: B-cell maturation antigen; IMWG: International Myeloma Working Group; MM: multiple myeloma; RRMM: relapsed or refractory multiple myeloma; SC: subcutaneous; ​​​​QW: once-weekly; Q2W: once every 2 weeks; ULN: upper limit of normalReferences:ELREXFIO® Summary of Product Characteristics.Kumar S, et al. Lancet Oncol. 2016;17:e328-3346. 
Efficacy OutcomesDeep and durable responses were observed in some BCMA-directed therapy-naïve patients treated with ELREXFIO®*†1
*Deep response defined as ≥CR.†As assessed by BICR.1
Read moreLoading
Efficacy Outcomes MagnetisMM-3 Study Follow-up Analyses Outcomes Read moreLoading
PP-L1A-GBR-0551. January 2025

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

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