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A Study to Examine the Effects of Novel Therapy Linvoseltamab in Combination With Other Cancer Treatments for Adult Participants With Multiple Myeloma That is Resistant to Current Standard of Care Treatments

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NCT05137054 · readout in 584 d

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

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
317estimated
Sites
42
Countries
France, Greece, Israel +2

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
Start2022-08-17actualWhen the study began enrolling
Primary completion2028-03-25estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2032-03-24estimatedThe whole study's end, after follow-up
First posted2021-11-30actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-08actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Multiple Myeloma

Interventions

  • Drug: Linvoseltamab — also filed as REGN5458, Lynozyfic™
  • Drug: Daratumumab — also filed as Darzalex®; Darzalex Faspro™
  • Drug: Carfilzomib — also filed as Kyprolis®
  • Drug: Lenalidomide — also filed as Revlimid®
  • Drug: Bortezomib — also filed as Velcade®
  • Drug: Pomalidomide — also filed as Imnovid, Pomalyst®
  • Drug: Isatuximab — also filed as Sarclisa®
  • Drug: Fianlimab — also filed as REGN3767
  • Drug: Cemiplimab — also filed as LIBTAYO, REGN2810
  • Drug: Nirogacestat — also filed as PF-03084014
  • Drug: Cevostamab — also filed as BFCR4350A, RO7187797

Primary outcomes

what the primary-completion date above is the date OF
Incidence of Dose Limiting Toxicities (DLTs) for each study regimen during the observation period
measured Up to 28 Days
Incidence of Treatment-Emergent Adverse Events (TEAEs)
measured Up to 5 Years
Severity of TEAEs
measured Up to 5 Years
Incidence of Serious Adverse Events (SAEs)
measured Up to 5 Years
Severity of SAEs
measured Up to 5 Years
Incidence of Adverse Events of Special Interest (AESIs)
measured Up to 5 Years
Severity of AESIs
measured Up to 5 Years
Incidence of laboratory abnormalities
measured Up to 5 Years

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