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 ANTIGEN×CD3¿DIRECTED BISPECIFIC ANTIBODY THERAPY

Registry ID
TAK-339-3001
Source registry
HEALTH_CANADA
Status
Ongoing
Phase
PHASE3
Study type
INTERVENTIONAL
Sponsor
TAKEDA DEVELOPMENT CENTER AMERICAS INC
Start date
2026-04-16
Last update
2025-07-16

Conditions

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