drugset / Trial / NCT04246047

Evaluation of Efficacy and Safety of Belantamab Mafodotin, Bortezomib and Dexamethasone Versus Daratumumab, Bortezomib and Dexamethasone in Participants With Relapsed/Refractory Multiple Myeloma

NCT04246047

Phase 3 Active not recruiting 494 enrolled GlaxoSmithKline
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a Phase 3, randomized, open-label study designed to evaluate safety and efficacy of belantamab mafodotin in combination with bortezomib/dexamethasone (Arm A) versus daratumumab in combination with bortezomib/dexamethasone (Arm B) in the participants with relapsed recurrent multiple myeloma.

Timeline

Start
2020-05-07
Primary completion
2023-10-02
Completion
2028-06-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Belantamab mafodotin Monoclonal antibody 2.5 mg/kg Intravenous
Comparator Daratumumab Monoclonal antibody 16 mg/kg Intravenous
Background Bortezomib Small molecule 1.3 mg/m2 Subcutaneous
Background Dexamethasone Small molecule 20 mg Oral

Indications