drugset / Trial / NCT06993675

Engaging T-cells to Eliminate MRD in Newly Diagnosed Myeloma Optimizing Response With Talquetmab and Teclistamab (ROTATE)

NCT06993675

Phase 2 Recruiting 50 enrolled Noffar Bar Johnson & Johnson · collab
NaSingle-groupOpen-labelTreatment

Summary

Multiple myeloma is characterized by a pattern of recurrent relapse and remains an incurable malignancy. Participants with minimal residual disease (MRD) after front line therapy with induction and transplant have worse prognosis than those with MRD negative disease. Bispecific T-cell-based immunotherapies have the potential to promote further reduction of malignant plasma cells thus improving rates of MRD negativity and improve patient outcomes. In this study, participants who are MRD positive after front line therapy will receive consolidation with GPRC5D-targeted bispecific talquetamab. We will test MRD negative conversion and if MRD negativity was not achieved, the participant will switch to a different target using the B-cell maturation antigen TCE, teclistamab. Consolidation will be continued for up to 1 year in participants who have achieved MRD negativity. After consolidation therapy on this protocol is complete, participants may continue to be treated with standardof- care (SOC) maintenance therapy.

Timeline

Start
2025-08-21
Primary completion
2029-08
Completion
2029-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Talquetamab Monoclonal antibody Subcutaneous
Subject Teclistamab Monoclonal antibody Subcutaneous

Indications