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

Outcome

Met primary endpoint

registry analysis (superiority test); Belantamab Mafodotin + Bortezomib (Bor) + Dexamethasone (Dex) vs Daratumumab + Bor + Dex; p <0.00001; Hazard Ratio (HR) 0.41 (95% CI 0.31 to 0.53) NCT04246047 ↗

paper CONCLUSIONS: As compared with DVd therapy, BVd therapy conferred a significant benefit with respect to progression-free survival PMID 38828933 ↗

release “The application is based on interim results from the DREAMM-7 and DREAMM-8 phase III trials, which both met their primary endpoints” gsk.com ↗

release “statistically significant and clinically meaningful progression-free survival (PFS) results for Blenrep combinations versus standards of care in both trials and overall survival (OS) in DREAMM-7” gsk.com ↗

release “In DREAMM-7, the Blenrep combination (n=243) nearly tripled median PFS versus the daratumumab-based comparator (n=251) (36.6 months versus 13.4 months, respectively” gsk.com ↗

release “Both DREAMM-7 and DREAMM-8 showed statistically significant and clinically meaningful PFS improvements for the Blenrep combinations” gsk.com ↗

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