drugset / Trial / NCT05060627

Study of Belantamab Mafodotin in Combination With Kd for the Treatment of Relapsed Myeloma Patients, Refractory to Lenalidomide

NCT05060627

Phase 1/2 Active not recruiting 60 enrolled PETHEMA Foundation Adknoma Health Research · collab
NaSequentialOpen-labelTreatment

Summary

This is a phase I-II open-label, multicenter, non-randomized study aiming to evaluate the efficacy and safety of belantamab mafodotin in combination with carfilzomib (Kyprolis®) and dexamethasone (Kd). Since this is the first time that this combination is being evaluated in a clinical trial, a first dose escalation part will be developed following the classic 3+3 design, to establish the maximum tolerated dose (MTD) of the combination. Once the MTD will be defined, a dose expansion phase will be open to recruit up to 60 patients. Patients will receive treatment with belantamab-mafodotin + Kd, until unacceptable toxicity, disease progression, patient withdrawal, loss to follow-up, end of study, or death.

Timeline

Start
2021-12-20
Primary completion
2024-10-23
Completion
2028-05-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Belantamab mafodotin Monoclonal antibody 1.9 mg/kg Intravenous
Subject Belantamab mafodotin Monoclonal antibody 2.5 mg/kg Intravenous
Subject Carfilzomib Other / unclassified 45 mg/m2 Intravenous
Subject Carfilzomib Other / unclassified 56 mg/m2 Intravenous
Subject Carfilzomib Other / unclassified 70 mg/m2 Intravenous
Subject Dexamethasone Small molecule 20 mg
Subject Dexamethasone Small molecule 40 mg

Indications