drugset / Trial / NCT05123131

Isa-RVD Study in Patients With Newly Diagnosed Multiple Myeloma

NCT05123131

NaSingle-groupOpen-labelTreatment

Summary

This study aims to evaluate the stringent Complete Response (sCR) rate by the end of two cycles of induction treatment, defined as the proportion of patients who have achieved sCR, according to International Myeloma Working Group (IMWG) criteria, by the end of two cycles of induction treatment.

Timeline

Start
2022-04-01
Primary completion
2025-06-24
Completion
2027-12-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Bortezomib Small molecule 1.3 mg/m2 Subcutaneous
Subject Dexamethasone Small molecule 20 mg Intravenous
Subject Isatuximab Monoclonal antibody 10 mg/kg Intravenous
Subject Lenalidomide Other / unclassified 10 mg Oral
Subject Lenalidomide Other / unclassified 25 mg Oral

Indications