drugset / Trial / NCT04808037

Blmf, Lenalidomide and Dexamethasone in Transplant-ineligible Patients With Newly Diagnosed Multiple Myeloma

NCT04808037

Phase 1/2 Active not recruiting 66 enrolled Hellenic Society of Hematology GlaxoSmithKline · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a phase 1/2, open label, study designed to assess the safety and clinical activity of different Belantamab Mafodotin doses in combination with lenalidomide and dexamethasone.

Timeline

Start
2021-02-22
Primary completion
2028-09-08
Completion
2028-11-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Belantamab mafodotin Monoclonal antibody 1.4 mg/kg
Subject Belantamab mafodotin Monoclonal antibody 1.9 mg/kg
Subject Belantamab mafodotin Monoclonal antibody 2.5 mg/kg

Indications