drugset / Trial / NCT05064358

Study to Investigate Alternative Dosing Regimens of Belantamab Mafodotin in Participants With Relapsed or Refractory Multiple Myeloma

NCT05064358

Phase 2 Completed 177 enrolled GlaxoSmithKline
RandomizedParallel-groupOpen-labelTreatment

Summary

This study aims to evaluate alternative dosing regimens of single-agent belantamab mafodotin in participants with relapsed or refractory multiple myeloma (RRMM) to determine if an improved overall benefit/risk profile can be achieved by modifying the belantamab mafodotin dose, schedule, or both.

Timeline

Start
2022-03-03
Primary completion
2024-08-19
Completion
2026-02-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Belantamab mafodotin Monoclonal antibody

Indications