A Multicenter, Randomized, Controlled, Open-label, Group-Sequential, Phase III 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 Antigen�CD3?Directed Bispecific Antibody Therapy
Study Type: Treatment
Phase: III
NCTID: NCT06980480
Principal Investigator:
Jenny Bhurtel