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Primary Immunodeficiency Diseases clinical trials at UC Irvine

1 in progress, 0 open to eligible people

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  • About How TAK-881 is Processed by the Body and Side Effects in People With Primary Immunodeficiency Diseases

    Sorry, in progress, not accepting new patients

    The main aim of this study is to compare the pharmacokinetics (PK) of subcutaneous (SC) administration of TAK-881 with HYQVIA in participants with chronic inflammatory demyelinating polyradiculoneuropathy (CIDP). The participants who are already receiving intravenous immunoglobulin G (IGIV)/conventional subcutaneous intravenous immunoglobulin G (cIGSC) will be treated with HYQVIA or TAK-881 with the same dose and dosing interval of immunoglobulin for up to 24 weeks. Participants will need to visit the clinic every 3 or 4 weeks during the duration of the study.

    Irvine, California and other locations

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