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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
