LINKER-MM4

Phase 1/2 Study of Linvoseltamab (Anti-BCMA X Anti-CD3 Bispecific Antibody) in Previously Untreated Patients With Symptomatic Multiple Myeloma

Published Results

Linvoseltamab Generates Responses in Newly Diagnosed Myeloma

The LINKER-MM4 trial enrolled 45 adult patients with previously untreated, symptomatic multiple myeloma. The cohort included both transplant-eligible (62.2%) and transplant-ineligible patients. As of the September 15, 2025, data cutoff, the median follow-up was 11.2 months for the phase 1a dose-escalation cohort and 4.8 months for the phase 1b dose-expansion cohort.

Responses were rapid, with a median time to partial response or better of 1.2 months.

Among the 43 patients evaluable for response:

  • 56% achieved a very good partial response (VGPR) or better.
  • 26% achieved a complete response (CR) or better.
  • 82% of patients who achieved a CR did so within 6 months of treatment initiation.

The efficacy data indicated a dose-dependent response. Patients in the 200 mg cohort (n = 21) demonstrated higher response rates compared with the 50 mg cohort (n = 20), with 86% vs 70% ORR, respectively. At the time of analysis, all patients remained progression-free.

2025-12-08T00:00:00ZRead more
(888) 850-0650

Real People. Real Support.

Need help connecting with this clinical trial? We're here to help!

Print a patient-friendly report to share with your patient.

We can help answer any questions and connect you (or your patient) with the study team.

Schedule a time that is convenient and we’ll call you to see how we can help you and your patient.