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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

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NCT05730036 · readout in 2,435 d

Sponsored by Regeneron Pharmaceuticals (industry) · REGN — their whole pipeline →.

Phase
Phase 3
Status
Recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
410estimated
Sites
159
Countries
Australia, Belgium, Brazil +15

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2023-09-18actualWhen the study began enrolling
Primary completion2033-04-19estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2033-04-19estimatedThe whole study's end, after follow-up
First posted2023-02-15actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-03-06actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Relapsed Refractory Multiple Myeloma (RRMM)

Interventions

  • Drug: Linvoseltamab — also filed as REGN5458, Lynozyfic™
  • Drug: Elotuzumab — also filed as Empliciti
  • Drug: Pomalidomide — also filed as Pomalyst
  • Drug: Dexamethasone — also filed as Decadron

Primary outcome

what the primary-completion date above is the date OF
Progression Free Survival (PFS) per International Myeloma Working Group (IMWG) response criteria determined by Independent Review Committee (IRC) in CD38 antibody exposed participants
measured Up to approximatively 5 years

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