drugset / Trial / NCT07671287

GMMG-HD11/DSMM XXI/64007957MMY3010

NCT07671287

Phase 3 Not yet recruiting 399 enrolled University of Heidelberg Medical Center
RandomizedParallel-groupOpen-labelTreatment

Summary

This is an open-label, randomized interventional multicenter Phase 3 clinical trial to investigate the efficacy and safety of Tec-DRd induction therapy and fixed-duration Tec-D maintenance post ASCT in adult participants with TE NDMM, compared with the SoC PERSEUS regimen. A total of 399 participants with TE NDMM aged ≥18 and ≤70 years and an Eastern CooperativeOncology Group (ECOG) status 0-2 will be included. The primary objective of the clinical trial: To determine the efficacy of Tec-DRd compared to DVRd after 6 cycles of induction/consolidation therapy and HD melphalan and ASCT, before start of maintenance therapy in participants with TE NDMM. Endpoint: Cumulative MRD negativity by NGS at a sensitivity level of 10-6 before start of maintenance therapy.

Timeline

Start
2026-06-30
Primary completion
2031-02-14
Completion
2033-01-30

Drugs

EvaluationDrugModalityDoseRoute
Comparator Bortezomib Small molecule Subcutaneous
Subject Teclistamab Monoclonal antibody Subcutaneous
Background Daratumumab Monoclonal antibody Subcutaneous
Background Lenalidomide Other / unclassified Oral
Background dexamethsone Unknown Intravenous

Indications