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Takeda's HyQvia receives EC approval for rare neuromuscular disorder CIDP

Takeda's HyQvia receives EC approval for rare neuromuscular disorder CIDP
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Kristina Allikmets , Giles Platford , Takeda Hyqvia , European Commission , Drug Administration , Plasma Derived Therapies Business Unit ,

Takeda's HYQVIA® Approved by European Commission as Maintenance Therapy in Patients with Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) | Region

OSAKA, Japan & CAMBRIDGE, Mass. (BUSINESS WIRE) Jan 29, 2024 ....

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Takeda's HYQVIA® Approved by European Commission as Maintenance Therapy in Patients with Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) | Business

OSAKA, Japan & CAMBRIDGE, Mass. (BUSINESS WIRE) Jan 29, 2024 ....

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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. ....

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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. ....

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