Linvoseltamab vs. Standard Treatment for Relapsed/Refractory Multiple Myeloma

This study is comparing an experimental drug called linvoseltamab (also known as REGN5458) to a combination of three standard drugs: elotuzumab, pomalidomide, and dexamethasone. We want to learn which treatment works better for adults with multiple myeloma that has come back or gotten worse after previous treatments (relapsed/refractory multiple myeloma). Linvoseltamab has shown promise in earlier studies, shrinking tumors in some patients who had no other good treatment options. The main goal is to see how long patients live without their cancer getting worse (Progression Free Survival). We are looking for about 410 participants who are 18 or older and meet certain health criteria. The current recruitment status is unclear.

Study design
This interventional study plans to enroll about 410 participants. It is comparing two different treatment approaches.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed for up to approximately 5 years to monitor how long they live without their cancer getting worse.

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NCT05730036

A Trial to Learn How Well Linvoseltamab Works Compared to the Combination of Elotuzumab, Pomalidomide and Dexamethasone for Adult Participants With Relapsed/Refractory Multiple Myeloma

Recruiting
PHASE3Ages 18+InterventionalTreatment
Regeneron Pharmaceuticals
~410 participants
Updated 2026-03-06 on ClinicalTrials.gov
What's tested:LinvoseltamabElotuzumabPomalidomideDexamethasone

At a glance

Recruiting sites
20 of 159 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Progression Free Survival (PFS) per International Myeloma Working Group (IMWG) response criteria determined by Independent Review Committee (IRC) in CD38 antibody exposed participants
Measured over Up to approximatively 5 years
Relapsed Refractory Multiple Myeloma (RRMM)
159 sites across 85 states
Spain11
Taiwan9
Italy7
South Korea7
Brazil5
Israel5
United Kingdom5
Santiago Metropolitan4
  • Clinical Trial Management · STUDY_DIRECTOR · Regeneron Pharmaceuticals

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  • Progression Free Survival (PFS) per International Myeloma Working Group (IMWG) response criteria determined by Independent Review Committee (IRC) in CD38 antibody exposed participantsUp to approximatively 5 years