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In May 2026, the company reported positive Phase II/III trial results for its investigational next-gen immune drug TAK-881 (immune globulin subcutaneous (human), 20% solution (SCIG 20%) with recombinant human hyaluronidase), which showed comparable efficacy, safety and immune protection to its existing lower dose immune globulin therapy HyQvia (immune globulin infusion (human) 10% with recombinant human hyaluronidase) in primary immunodeficiency disease, while offering the potential for lower infusion volumes and shorter treatment times.

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