NCT04483739: Phase 3: EMN 24 - Isa-KRd vs KRd New Multiple Myeloma Eligible for ASCT - IsKia TRIAL
Updated: Jan 27
(IsKia TRIAL) (IsKia) - (EMN24/HOVON503)
NCT04483739: Phase 3: Isa-KRd vs KRd in Newly Diagnosed Multiple Myeloma Patients Eligible for Autologous Stem Cell Transplantation (IsKia TRIAL) (IsKia)
IsKia trial (EMN24/HOVON503)
Isa-KRd vs KRd in Newly Diagnosed Multiple Myeloma Patients Eligible for Autologous Stem Cell Transplantation (IsKia TRIAL) (IsKia)
This protocol is a phase III study designed to compare the efficacy and the safety of Isa-KRd induction, transplant, Isa-KRd post ASCT consolidation and Isa-KRd light consolidation vs KRd induction, transplant, KRd post ASCT consolidation and KRd light consolidation After confirmation of eligibility criteria patients will be randomized to one of the 2 treatment groups in a 1:1 randomization ratio.
Sponsor
Collaborators
EMN Research Italy
ClinicalTrials.gov Identifier: NCT04483739
Official Title: Phase III Study of Isatuximab-Carfilzomib-Lenalidomide-Dexamethasone (Isa-KRd) Versus Carfilzomib-Lenalidomide-Dexamethasone (KRd) in Newly Diagnosed Multiple Myeloma Patients Eligible for Autologous Stem Cell Transplantation (IsKia TRIAL
First Posted: July 23, 2020
Click here for details on ClinicalTrials.gov
Drug: Carfilzomib Lenalidomide Dexamethasone
Drug: Isatuximab Carfilzomib Lenalidomide Dexamethasone
Locations:
Europe
Czechia
Germany
Greece
Italy
Netherlands
Norway
Spain
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