drugset / Trial / NCT04896658

Belantamab Mafodotin, Cyclophosphamide, and Dexamethasone in Relapsed/Refractory Multiple Myeloma

NCT04896658 ↗

Phase 1/2 Terminated 10 enrolled University of Maryland, Baltimore
Non-randomizedSequentialOpen-labelTreatment

Summary

Evaluate the efficacy and safety of Belantamab Mafodotin, cyclophosphamide, and dexamethasone in patients with Relapsed/Refractory Multiple Myeloma

Timeline

Start
2021-12-03
Primary completion
2023-06-30
Completion
2024-12-01

Outcome

Outcome not reported

Stopped (Enrollment): “The study was terminated due to FDA withdrawal of the drug and lack of enrollment with available BCMA therapies that were deemed safer.”

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Belantamab mafodotin Monoclonal antibody 1.9 mg/kg —
Subject Belantamab mafodotin Monoclonal antibody 2.5 mg/kg —
Subject Cyclophosphamide Other / unclassified 300 mg —
Subject Cyclophosphamide Other / unclassified 500 mg —
Background Dexamethasone Small molecule 40 mg —