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Takeda's HYQVIA® Approved by European Commission as Maintenance Therapy in Patients with Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) -January 29, 2024 at 02:01 am EST

HYQVIA [Immune Globulin Infusion 10% with Recombinant Human Hyaluronidase] becomes the Only Facilitated Subcutaneous Immunoglobulin, Offering Patients an up to Once-Monthly Treatment...
United States Kristina Allikmets Demyelinating Polyneuropathy Research Development For Takeda Plasma Committee For Medicinal Products Human Use European Commission

Takedas HYQVIA Approved by European Commission as Maintenance Therapy in Patients with Chronic Inflammatory Demyelinating Polyneuropathy CIDP

Takeda TSE4502NYSETAK today announced that the European Commission EC approved HYQVIA Immune Globulin Infusion 10 Human with Recombinant Human Hyaluronidase as maintenance therapy in patients of all ages with chronic inflammatory demyelinating polyneuropathy CIDP after stabilization with intravenous immunoglobulin therapy IVIG.
United States Kristina Allikmets Demyelinating Polyneuropathy European Medicines Agency Peripheral Nerve Society Clinical Program

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