drugset / Trial / NCT05900882

SVRd for the Treatment of Newly Diagnosed Multiple Myeloma Patients Presenting With Extramedullary Disease

NCT05900882

NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of SVRd in NDMM patients presenting with extramedullary disease.

Timeline

Start
2022-07-15
Primary completion
2025-08-30
Completion
2025-08-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Bortezomib Small molecule 1.3 mg/m2 Intravenous
Subject Dexamethasone Small molecule 20 mg Oral
Subject Lenalidomide Other / unclassified 25 mg Oral
Subject Selinexor Other / unclassified 60 mg Oral

Indications