Clinical Trial

Trial Protocol ID USOR 24073: R/R 2L+ MM Ph3 Study comparing teclistamab monotherapy vs pomalid or carfilzomib MM

Trial Description

A Phase 3 Randomized Study Comparing Teclistamab Monotherapy versus Pomalidomide, Bortezomib, Dexamethasone (PVd) or Carfilzomib, Dexamethasone (Kd) in Participants with Relapsed or Refractory Multiple Myeloma who have Received 1 to 3 Prior Lines of Therapy, Including an Anti-CD38 Monoclonal Antibody and Lenalidomide (MajesTEC-9)

MOA: Teclistamab is a BCMA x CD3 bispecific antibody.

Key Eligibility Criteria:

  • Documented diagnosis of relapsed or refractory multiple myeloma that is measurable
  • Subject should have received 1 to 3 prior lines of antimyeloma therapy
    • Minimum of 2 consecutive cycles of an anti-CD38 monoclonal antibody at approved dosing schedule
    • Minimum of 2 consecutive cycles of lenalidomide in any prior line
  • ECOG score ≤ 2
  • Subjects that received any prior BCMA-directed therapy are excluded
  • Subject that received prior pomalidomide therapy and do not meet bortezomib retreatment criteria are not allowed on PCd
  • Subjects with prior carfilzomib therapy are not allowed on Kd

Contact us regarding Clinical Trials at MOHRSCH@usoncology.com or call us at 877-664-7724

Investigator

  • Vinni Juneja, MD

Disease Types

Sponsor

  • Janssen

ClinicalTrials.gov NCT ID

  • NCT05572515