VICD

Bortezomib, Isatuximab, Cyclophosphamide and Dexamethasone Induction in Transplant-Eligible Multiple Myeloma Patients (VICD)

What will happen during the trial?

The study hypothesis is that the isatuximab plus bortezomib, cyclophosphamide and dexamethasone (VCD) combination is safe and highly effective even in those with renal insufficiency (RI) from myeloma. In this study, we seek to improve the efficacy of VCD by adding isatuximab in newly diagnosed multiple myeloma patients undergoing autologous stem cell transplant (ASCT) irrespective of renal function.

The primary objective is to determine if the addition of isatuximab to VCD will increase the proportion of subjects achieving very good partial response (VGPR), as defined by the International Myeloma Working Group (IMWG) criteria and by the time of completion of post-ASCT consolidation treatment.

More Information

Trial Status
Accepting patients
Trial Phase
Phase 2
Enrollment
41 patients (estimated)
Sponsors
Medical College of Wisconsin
Tags
Monoclonal Antibody, CD38, Pre-Autologous Stem Cell Transplant
Trial Type
Treatment
Last Update
2 months ago
SparkCures ID
1153
NCT Identifier
NCT04240054

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