drugset / Trial / NCT04140162

Phase 2 Study With Minimal Residual Disease (MRD) Driven Adaptive Strategy in Treatment for Newly Diagnosed Multiple Myeloma (MM) With Upfront Daratumumab-based Therapy

NCT04140162 ↗

NaSingle-groupOpen-labelTreatment

Summary

This phase 2 trial will test whether the combination of DaraRd (daratumumab + lenalidomide + dexamethasone) as induction therapy, followed by DRVd (daratumumab + lenalidomide + bortezomib + dexamethasone) consolidation therapy, if needed, will result in more patients achieving minimal residual disease (MRD)-negative status, relative to the standard of care. Consolidation therapy will be administered only to those patients with MRD-positive status after induction therapy. This is a study based on adaptive design for decision making of treatment options. Duration of therapy (daratumumab cycles) will depend on individual approach, response, evidence of disease progression and tolerance.

Timeline

Start
2020-10-05
Primary completion
2024-05-02
Completion
2026-05-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Bortezomib Small molecule 1.5 mg/m2 Subcutaneous
Subject Daratumumab Monoclonal antibody 16 mg/kg Intravenous
Subject Daratumumab Monoclonal antibody 1800 mg Intravenous
Subject Dexamethasone Small molecule 20 mg Oral
Subject Dexamethasone Small molecule 40 mg Oral
Subject Lenalidomide Other / unclassified 10 mg Oral

Indications