IGI 10% (TAK-339)
A Multicenter, Randomized, Controlled, Open-label, Group-Sequential, Phase 3 Study to Investigate the Efficacy, Safety, and Tolerability of Intravenous Gammagard Liquid (Immune Globulin Infusion, 10%) for Primary Infection Prophylaxis Compared With Secondary Infection Prophylaxis in Adult Subjects With Multiple Myeloma Receiving B-Cell Maturation AntigenxCD3-Directed Bispecific Antibody Therapy
Arms / Cohorts
Experimental:Primary Infection Prophylaxis: IGI, 10%
Not yet accepting
Active Comparator:Secondary Infection Prophylaxis: IGI, 10%
Not yet accepting
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