Video content above is prompted by the following question:
- Discuss the data presented at EHA 2024 on the efficacy and safety of teclistimab in patients with relapsed/refractory multiple myeloma (RRMM) with high-risk features: a subgroup analysis of the phase 1/2 MajesTEC-1 study. (Abstract)
- What was the objective of the subgroup analysis of this study?
- How was this study designed/what methodology was used?
- What results were presented?
- N=165
- N=24 aged ≥75 years
- N=20 ISS stage III
- N=38 high-risk cytogenetics
- N=28 extramedullary disease
- N=18 bone marrow plasma cells
- N=50 penta-drug refractory
- Median follow up ~30 months across subgroups
- Objective Response Rate (ORR)
- Median duration of response (mDOR)
- Safety