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Takeda Presents Phase 2/3 IgGNITE Study Results of Investigational Subcutaneous TAK-881 in Primary Immunodeficiency Disease (PID) at ESID 2026
Source: Business Wire
Healthcare & BiotechCompany Fundamentals
Takeda presented Phase 2/3 study results for TAK-881 in primary immunodeficiency, reporting comparability to HYQVIA with 50% less immunoglobulin (IG) volume. The brief report provides no further efficacy, safety, or market-reaction details.
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